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 Building Stronger Teams Through Accountability -A One Day Workshop for Technology Managers

 

Category: TECHNICAL/ENGINEERING - Management

In this one day session, you'll take the first step towards developing your skills when it comes to accountability. You'll learn how to effectively deal with the finger pointing that takes place when something goes wrong, how to encourage your team to suggest positive change just by asking the right questions, and how to gain the trust and admiration of your team in your everyday work life. Take the first step towards building an accountable, high performing team that compensates for each others' bad days...Join us!


 

 10-Hour OSHA Compliance Course

 

Category: SECURITY/SAFETY

Earn your 10-Hour OSHA course completion card with 2 days of in-depth training!


 

 21 CFR Part 11 Compliance for SaaS/Cloud Applications

 

Category: Compliance-Regulation

The instructor will address the latest computer system industry standards for data security,data transfer,computer system validation related to FDA 21 CFR Part 11, European Annex 11, and HIPAA electronic security regulations for patient medical records.


 

 21 CFR Part 11/Annex 11 compliance for software validation and SaaS: In-person Seminar

 

Category: Compliance-Regulation

This interactive one-day course explores proven techniques for reducing costs associated with implementing, using, and maintaining computer systems in regulated environments.


 

 4th Annual ComplianceOnline Medical Device Summit 2018

 

Category: Compliance-Regulation

Learn More about Medical Device Global Regulatory Landscape and Off-label Promotion and Explore Upcoming Changes in Medical Devices under Trump Administration.


 

 A Comprehensive View of FDA Regulations for Medical Devices: 2 - Day In-Person Seminar

 

Category: Compliance-Regulation

The seminar will help you understand the four major parts of the US regulatory structure: laws regulations, guidance, and consensus standards. Risk class and the panels, established by law, characterize medical devices in the US.


 

 A risk based approach to GxP Compliant Laboratory Computerized Systems

 

Category: Compliance-Regulation

This hands-on seminar provides a practical, risk based approach to laboratory computerized system specification, verification, and implementation.


 

 Accounts Receivable/Consumer Debt Collection - From Delinquency to Bankruptcy

 

Category: Compliance-Regulation

Consumer debt collection is among the most regulated areas of business there is. In fact, the United States is known to be


 

 Advanced Lending, Deposit & Operations Seminar

 

Category: Compliance-Regulation

An in-depth look at complex and emerging compliance issues for more experienced compliance professionals. Class consists of lectures, with in-depth analysis of the laws and regulations, along with exercises and sample policies and relevant guidance.


 

 Advertising Research

 

Category: MARKETING - Marketing Research

In this seminar you will learn how marketing research techniques are used at the various stages of development and evaluation of print and broadcast advertising.


 

 Aerospace Program Management - It's More than Scheduling and Delivery

 

Category: Compliance-Regulation

Effective and efficient management of today's complex and integrated programs requires both the refinement of interpersonal and basic leadership skills as well as the application of appropriate technologies and tools.


 

 AML/BSA Boot Camp

 

Category: Compliance-Regulation

Attend this AML/BSA Boot Camp to learn 4 pillars of BSA, roles of FinCEN, OFAC and the USA Patriot Act. The workshop will focus on framework, education and tools needed to manage BSA/AML.


 

 An OSHA Compliance Update

 

Category: SECURITY/SAFETY

You’ll get a highly informative crash course in the legal basics of OSHA … what’s expected, what’s changed, where there are loopholes and where your company may be veering off course.


 

 Analyze Safety In The Workplace:  Inspections, Management Techniques & Training Methods: In-person Seminar

 

Category: Compliance-Regulation

This one day seminar will be jammed packed with numerous lessons learned applications, case studies and illustrations that showcase successful analyzation of safety inspection, management and training methods.


 

 Analyzing and Satisfying Requirements Creating and Validating Solutions That Deliver Business Results

 

Category: COMPUTERS / IT - Systems Management

The ultimate objective of a business analysis, process improvement or information technology project is to improve business results. Business process analysis techniques will be used to convert raw requirements data into the capabilities of the solution.


 

 Applications of Statistics to Pharmaceutical Operations with Explanatory Statistics and Sampling Software

 

Category: Compliance-Regulation

Understand the statistics methodologies associated with risk-based qualification of instruments and equipment, and validation of test methods and manufacturing processes.


 

 Applying Research & Insights: Customer, Brand Product

 

Category: MARKETING - Marketing Research

This seminar will provide a broad understanding of some of the most important applications found in marketing research, including segmentation, positioning, pricing, customer satisfaction, advertising and new product research.


 

 Associate in Human Resources Generalist Certificate Program

 

Category: Compliance-Regulation

Join us In-Person in Greenville, SC or Online via Live Stream / Webinar for our Instructor-Led 2-Day Associate in Human Resources Generalist Certificate Program.


 

 Attorney's Guide to Legal Research Strategies On- and Offline

 

Category: LAW - Legal Research

Join your colleagues in an engaging discussion of the latest challenges and opportunities evolving technology presents in legal research and law practice management.


 

 Bad Things Happen, But It Can Get Worse - Understanding FDA Post Market Regulations

 

Category: Compliance-Regulation

This Seminar will have you stop spinning your wheels with nonessential activities, and leave you with a comprehensive learning package that has only been offered by Casper Uldriks and Rita Hoffman, who bring over 68 years of combined experience.


 

 Basel III, IV and Beyond - Effective Risk Data Management and Reporting

 

Category: FINANCE/INVESTING - Risk Management

This training program will cover the most significant standards and guidelines issued by the Basel Committee on Banking Supervision and discuss the most effective strategies for their implementation.


 

 Best in Class Wage & Hour Compliance: The Federal Labor Standards Act (FLSA)

 

Category: Compliance-Regulation

Your participation in this seminar will assist you in ensuring wage and hour laws are being followed properly in your organization.


 

 BSA/AML/OFAC Risk Assessments - Are You Doing Them Correctly

 

Category: Compliance-Regulation

This Bank Secrecy Act risk assessment seminar will highlight BSA best practices that are being acknowledged and recognized by regulators and examiners and will discuss each risk assessment area.


 

 Building a Vendor Qualification Program for FDA Regulated Industries: One and Half Day In-Person Seminar

 

Category: Compliance-Regulation

This course will provide valuable assistance and guidance to all FDA regulated companies for building sustainable vendor qualification program


 

 CA HR 101 - HR Generalists and CA Supervisors Too

 

Category: HR MGMT - Training Development

Attend this seminar to get comprehensive knowledge on California compliance employment problems, discrimination and harassment, leave in CA (CFRA, FMLA, pregnancy leave), and different acts like Pregnancy Disability Leave (PDL), California Family Rights Act (CFRA), Family Medical Leave Act (FMLA), California New Parent Leave Act.


 

 CA&PA for Medical Devices

 

Category: Compliance-Regulation

This interactive two-day course provides the tools you need to develop and implement an effective medical device CA&PA system.


 

 CAL/OSHA 30-Hour Compliance Course (5-day)

 

Category: SECURITY/SAFETY

Earn your 30-hour Cal/OSHA course completion card with 5 days of in-depth training that will increase your understanding of workplace safety initiatives and bring you up to speed on all of Cal/OSHA’s rules, regulations and guidelines.


 

 Cal/OSHA Compliance

 

Category: SECURITY/SAFETY

Discover dozens of cost-effective ways for getting your organization into compliance, learn how to expand the effectiveness of your safety training program, find out how to keep the meticulous records required by Cal/OSHA, and learn how to assess your organization for a variety of hazards.


 

 California Special Education Law

 

Category: LAW - School Law

Comply With the Latest Special Education Laws to Avoid Liability


 

 Certificate Program in FMLA & ADA Compliance - HR Law

 

Category: HR MGMT

Discover vital employment law knowledge, critical strategies to perfect your HR skills, and earn your certificate in FMLA, ADA, GINA compliance and best practices!


 

 China & Pacific Rim Markets : Compliance Processes for Life Science Products - Company Establishment, Clinical Trials, Registrations, Renewals and Supply Chain Considerations

 

Category: Compliance-Regulation

This course specifically focuses on the overall regulatory compliance requirements and procedures for Pharmaceuticals, Medical Devices, Biologics and Combination Products in China and the listed Pacific Rim Countries.


 

 CLIA Waiver and Dual 510(k) CLIA Waiver Submissions to FDA

 

Category: Compliance-Regulation

FDA has granted precious few applications for waiver since their CLIA Waiver guidance was published on January 30, 2008. Between 2008 and 2012, FDA reviewed 34 applications for CLIA Waiver and approved 14, sometimes taking years to issue a denial.


 

 Coaching Skills to Build Peak Performance

 

Category: GENERAL MGMT - Coaching/Mentoring/Counseling

Learn how to give both positive & negative feedback skillfully, facilitate problem solving discussions, help employees be their best by coaching, and how to get problem behavior changed.


 

 Collections and FDCPA Compliance: A Comprehensive Guide

 

Category: LAW - Collections

Experienced faculty will walk you through the collections process from start to finish, and after all is said and done, you will leave with the information needed to protect you or your client's bottom line.


 

 Complete 1099, TIN Matching, B-Notice, FATCA and Nonresident Alien 1042-S Compliance Update: 2-Day In-Person Seminar

 

Category: Compliance-Regulation

In this two day workshop, participants will learn how to identify independent contractors and non-resident aliens. attendees will learn the best method to process 1099 and 1042-S reporting to both your payees and the IRS using best practices.


 

 Compliance Risk Management in Medical Devices, Pharmaceuticals, and Combination Products

 

Category: Compliance-Regulation

Effective risk management is the hallmark of a successful corporation. Increasingly, it is also the hallmark of a compliant corporation.


 

 ComplianceOnline Pharma Summit 2016 – Risk Control and Compliance

 

Category: Compliance-Regulation

This summit will provide a venue for industry experts, policymakers, manufacturers, inventors and clinician to discuss and debate these challenges as well as explore new strategies and opportunities for growth.


 

 Computer System Validation - Reduce Costs and Avoid 483s

 

Category: Compliance-Regulation

This Computer System Validation Training course will explore proven techniques for reducing costs associated with implementing, using, and maintaining computer systems in regulated environments.


 

 Confined Spaces for General Industry. Lockout/Tagout

 

Category: Compliance-Regulation

This is a complete treatment of the Confined Spaces Standard from “A to Z”. (However we will not be training people to conduct Entry Rescue.) It is also a complete analysis of OSHA’s Lockout/Tagout Standard (formally called “Control of Hazardous Energy”).


 

 COSO Framework for Internal Controls, Risk Assessment and Financial Statement Audit: 2-Day In-Person Seminar

 

Category: Compliance-Regulation

This course will address the procedures for conducting a risk assessment for errors and fraud. It will review risks for financial statement preparation, operations, and compliance.


 

 Creating Reader-Focused Technical Documents in FDA Regulated Industries

 

Category: Compliance-Regulation

Advanced technology may have pushed effective communication to the wayside to make clear writing a lost art, now due for revival! In the Information Age, a surplus of technical data proliferates with very little information communicated in plain language.


 

 Data Integrity, Good Documentation Practices and Electronic Data Governance

 

Category: Compliance-Regulation

Three interactive modules that tackle the requirements and the discipline needed to consistently manually document and electronically record the manufacturing & testing of APIs, Drug Formulations, Biosimilars and Vaccines DATA INTEGRITY MEANS Manual Entries


 

 Data Integrity: FDA, WHO and EMA's Requirements: 2-Day In-person Seminar

 

Category: Compliance-Regulation

Data Integrity has become a non-compliance area often observed by the FDA and reported within Form FDA 483s and Warning Letters.


 

 Design History Files, Device Master Records and Quality Management System for Medical Device Company - Principles of Lean Documents and Lean Configuration

 

Category: Compliance-Regulation

During this seminar, the Theory of Lean Documents and its corollary applied to lean configuration will be applied in order to construct, write, and configure the types of documents and records necessary for medical device design and manufacturing.


 

 Designing and Managing Best-in-Class Customer Engagement Programs

 

Category: MARKETING - Marketing Research

This seminar deals with research methods designed to monitor customer satisfaction and to gain customer loyalty.


 

 Designing Effective Questionnaires: A Step by Step Workshop

 

Category: MARKETING - Marketing Research

This seminar will appeal to those individuals responsible for designing questionnaires within their own organization or working directly with MR suppliers.


 

 Developing Your Analytical Skills: How to Research and Present Information

 

Category: PERSONAL DEVELOPMENT

Quickly synthesize qualitative data, determine implications, and make informed decisions.


 

 Driving Operational Excellence Through The Organization using Quality Tools and Processes : One and a Half-day In-Person Seminar

 

Category: ORGANIZATIONAL DEVELOPMENT

This course provides an Overview of the structure with more in-depth analysis of the Methods & Philosophy, Culture, and Tools that are necessary for the start of Operational Excellence.


 

 Effective Quality Oversight of Pharmaceutical Contract Manufacturing Organizations (CMOs)

 

Category: Compliance-Regulation

This seminar will help all personnel responsible for CMO oversight understand how to manage CMOs- from start to finish. In-depth focus will be placed on Selection and Qualification, Quality Agreements, Understanding of CMO Operations.


 

 Effective Technical Writing

 

Category: COMMUNICATIONS - Writing Skills

Improve your technical writing—without compromising your technical message!


 

 Effectively Addressing and Remediating FDA's Form 483 Findings, Warning Letters and Consent Decree Compliance Issues

 

Category: Compliance-Regulation

This seminar will guide the attendee in effectively handling, addressing and remediating FDA's and other related compliance issues associated such as FDA's Form 483, Warning Letter and Consent Decree Compliance Findings.


 

 Employee Accountability

 

Category: GENERAL MGMT - People Management

An article in the March 11, 2010 edition of TIME magazine purported to explain “why we have entered the post-trust era.” Indeed, we seem to be in a time where people act inappropriately and then refuse to take responsibility for their actions. Who can we blame for the world economic crisis, or issues with religion, or the outcomes of our governments, or the state of the environment? More to the point, why do we spend so much time and energy looking to pin the blame on someone (usually anyone but ourselves)?With this in mind, it’s no wonder that organizations who promote accountability are more successful and more productive. In this one-day workshop, you will learn about what accountability is, how to promote it in your organization, and how to become more accountable to yourself and others.


 

 Employment Law

 

Category: EMPLOYMENT LAW

Stay up-to-date and compliant with the latest developments in labor and employment law


 

 Employment Law 101 for Managers and Supervisors

 

Category: EMPLOYMENT LAW - General Employment Law

Join your fellow managers at this dynamic one-day personnel law seminar designed for the everyday manager and supervisor. You’ll discover your important role in complying with critical employment laws and gain practical guidelines for legally managing your employees. This seminar is simply the best, most painless way to get the significant personnel law knowledge you need as a manager or supervisor today!


 

 Employment Laws Certificate Program: 2 Days in person Seminar

 

Category: Compliance-Regulation

This training contains everything our Managers and Supervisors need to know to succeed and to protect our organizations by complying with Employment Laws by doing the right thing from a moral, ethical and legal way.


 

 Expense Reporting Best Practices: One and a Half Day In-Person Seminar

 

Category: Compliance-Regulation

This inter-active session will be filled with real-life examples and attendees will have the opportunity to not only interact with other attendees but see how they’d treat different delicate situations.


 

 Exploring Data Integrity To Include FDA, WHO and EMA's Latest Guidance for Industry (2018/2019)

 

Category: Compliance-Regulation

Data Integrity has become a non-compliance area often observed by the FDA and reported within Form FDA 483s and Warning Letters.


 

 FDA Audit, Quality Assurance Practices, Responsibilities and Expectations

 

Category: Compliance-Regulation

This training will examine the differences between Quality Assurance and Quality Control and the responsibilities of each. In addition, attendees will discuss what characteristics quality personnel should possess.


 

 FDA Penalties for Non-Compliance in Pharma - 2017 case studies and Readiness for 2018

 

Category: Compliance-Regulation

This hands-on seminar provides a comprehensive approach to learning how to proactively prevent non-compliance.


 

 FDA Recalls - Before You Start, and After You Finish

 

Category: Compliance-Regulation

The seminar will cover critical performance targets for conducting an effective recall. You will learn how missteps in the recall process become an expensive problem in terms of money and a sloppy corporate image.


 

 FDA Regulations for Dietary Supplements Manufacturers (21 CFR Part 111, GMP and QMS)

 

Category: Compliance-Regulation

This course will show the FDA’s requirements for dietary supplement manufacturing and teach how to implement the concepts in a plant and manage the compliance requirements using the quality management system approach.


 

 FDA Requirements for Food Defense Planning and Implementation

 

Category: Compliance-Regulation

The seminar also will involve a detailed discussion of an acceptable Food Safety Plan to be developed by the companies which are covered by the Rule.


 

 FDA's GMP Expectations for Phase I and First-in-Man Clinical Trials

 

Category: Compliance-Regulation

Because a phase 1 clinical trial initially introduces an investigational new drug into human subjects, appropriate CGMP help ensure subject safety.


 

 FDA's Import Program for 2016 - New Pathways and Pitfalls: 2-Day In-Person Seminar by Ex-FDA Official

 

Category: Compliance-Regulation

The FDA continues to change its import program to better manage new problems and to use new procedures to make the whole process easier.


 

 FDA's Medical Device Software Regulation Strategy

 

Category: Compliance-Regulation

This seminar will help those involved in overcoming these commercial and regulatory obstacles. It will highlight the need for firms to remain current with technological tools and strategy to remain competitive, and ideally, outside FDA’s regulatory radar.


 

 FDA's New Import Program for 2019 - Strict Precision

 

Category: Compliance-Regulation

The FDA continues to change its import program to better manage new problems and to use new procedures to make the whole process easier.


 

 FDA's Refuse to Accept Policy - How to Prepare 510 (K) Submission to Avoid the Pitfalls of the Policy

 

Category: Compliance-Regulation

This 2 day course will show how to submit a traditional, abbreviated and special 510(k) for a Class II Medical Device. It will discuss what to look for in a predicate device and how to show substantial equivalence.


 

 FDCPA Compliance for the Indiana Practitioner

 

Category: ACCOUNTING - Credit/Collection

Collect What's Owed - Legally and Effectively


 

 Financial Reporting Disclosure Statements: 2-Day In-person Seminar

 

Category: FINANCE/INVESTING

Over the past decade, the nature of Financial Reporting Disclosures Statements has evolved to meet the needs of users. Business and markets have become more complex business models,


 

 Find it Free and Fast on the Net: Strategies for Legal Research on the Web

 

Category: LAW

Harness the Many Uses of the Internet


 

 FMLA and ADA Compliance Certificate Program: Everything You Ever Wanted to Know

 

Category: Compliance-Regulation

This is a thorough Certificate Program which will provide you with the tools and resources you need to maintain compliance with these two important laws and regulations and to serve as an internal consultant to minimize organizational risk.


 

 FMLA Compliance Update

 

Category: EMPLOYMENT LAW - General Employment Law

A good working knowledge of the FMLA is not enough. You need not only the very latest information on how court rulings and interpretations are changing your rights and obligations but also cutting-edge tools for applying the law decisively in your workplace.


 

 FMLA Compliance Update

 

Category: HR MGMT

Can you afford to make a mistake when it comes to FMLA?


 

 FMLA, ADA and PDA Certificate Program : 2-Day In-Person Seminar

 

Category: Compliance-Regulation

This is a thorough Certificate Program Training which will provide you with the tools and resources you need to maintain compliance with these three important laws and regulations and to serve as your organization internal consultant to minimize organizational risk.


 

 Focus Group Moderator Training

 

Category: MARKETING - Marketing Research

This workshop, designed to train you to become a focus group moderator, covers both the logistics to setting up groups and the skills required to lead groups and answer questions.


 

 Food labelling and advertising requirements for foods sold in Australia and New Zealand

 

Category: Compliance-Regulation

n this two day workshop conference you will learn of the mandatory Australian and New Zealand requirements in labelling a compliant food


 

 Forecasting Models for Customer Behavior and Lifetime Value

 

Category: MARKETING - Marketing Research

During this 2-day in-depth analytical seminar you will learn how to use readily available purchasing data to examine forward-looking aspects of customer behavior.


 

 Foreclosure Compliance: New Requirements and Advanced Issues

 

Category: LAW

Learn from our expert faculty and get tips and strategies to minimize risk, satisfy requirements and ensure a smooth flowing process.


 

 Fundamentals of Lending, Deposit and Operations Seminar

 

Category: Compliance-Regulation

Fundamental concepts in compliance with a strong, basic understanding of common compliance rules and regulations. Class will include lectures and exercises designed to reinforce the information that attendees learn in the class.


 

 Getting the Most Out of Traditional and Online Qualitative Research

 

Category: MARKETING - Marketing Research

Designed for individuals who design, commission, and manage focus group research, this course will cover all of the necessary requirements to setting up and determining which type of qualitative research techniques we should use, when and why.


 

 Healthcare Privacy and Security Regulations: Satisfying HIPAA, GDPR, 42 CFR Part 2, FERPA, and State Laws Protecting Health Information

 

Category: Compliance-Regulation

This session is designed to provide intensive, one and a half-day training in healthcare information privacy and security regulatory compliance, touching on the key regulations needing attention today.


 

 HIPAA - The Requirements for a Compliance Program

 

Category: Compliance-Regulation

Attendees will leave the course clearly understanding of all the requirements for a comprehensive HIPAA compliance program and what steps need to be taken to mitigate risk.


 

 HIPAA Compliance Boot Camp

 

Category: LAW - Health Care

Don't risk severe fines, sanctions and suits. Learn how you - and your clients - can remain effective in everyday practice while ensuring full compliance with HIPAA in this comprehensive program.


 

 HIPAA Compliance for Healthcare Professionals

 

Category: Healthcare - Coding billing

Learn the latest HIPAA Privacy and Security rules governing electronic record keeping and patient privacy


 

 HIPAA Privacy Rule Compliance-Understanding New Rules and Responsibilities of Privacy Officer

 

Category: Compliance-Regulation

This seminar will also explain audits and enforcement, and how privacy regulations relate to security and breach regulations, as well as responding to privacy and security breaches and ways to prevent them.


 

 HIPAA Security and Breach Rule Compliance- Understanding Risk Analysis, Policies and Procedures and Managing Incidents

 

Category: Compliance-Regulation

This session will also explain HIPAA Security safeguards and the role of risk analysis in effectively evaluating and implementing Security Rule compliance. Audits and enforcement will be explained, as well as security breaches and how to prevent them.


 

 How Enterprise Risk Management, Sustainability and ROI Work Together

 

Category: GENERAL/ADMINISTRATIVE SERVICES

We will explore a practical approach to implementing ERM and will learn which risk framework to adopt for your organization.


 

 How to build and validate Excel spreadsheets for GxP compliance

 

Category: Compliance-Regulation

This two-day seminar teaches how to develop and validate Excel spreadsheets for 21 CFR Part 11 compliance. This training event covers all of the required features that have to be configured in Excel.


 

 How to Comply with Cal/OSHA

 

Category: SECURITY/SAFETY

Attend this intensive workshop and gain the skills you need to protect your company from a costly compliance error.


 

 How to Comply with Cal/OSHA: A Two-Day Workshop

 

Category: SECURITY/SAFETY

Attend this intensive two-day Cal/OSHA workshop and gain the skills you need to protect your company from a costly compliance error


 

 How to Comply With California OSHA

 

Category: SECURITY/SAFETY

Attend this intensive two-day Cal/OSHA workshop and gain the skills you need to protect your company from a costly compliance error.


 

 How to Improve Employee Accountability

 

Category: GENERAL MGMT

This seminar will help you learn to flex your managerial skills to get everyone to pull together and work side by side to achieve the organization's goals in the most efficient, productive way possible.


 

 How to Pass the Customs Broker Exam

 

Category: Compliance-Regulation

This course will advise on the best investment of physical products (book rack, calculator, tabs, notes), teach the way Customs approaches the classification of products in their scenario based tests.


 

 HR Legal Compliance: Advanced Practice

 

Category: HR MGMT

This advanced guide to HR law will give you the skills you need to tackle employee leave complexities, internal investigation complications, workplace special event landmines and more.


 

 Human Resource Essentials - HR Compliance Certification Program

 

Category: Compliance-Regulation

I think I am not even half way with the list that HR Professionals are expected to do. Don’t you worry. You have found the right Certificate Program that will provide with all the tools necessary to be the best HR Professional one can be!


 

 Human Resources and Employment Law Essentials: 2-Day In-Person Seminar

 

Category: HR MGMT

This Human Resources and Employment Law Seminar will assist companies in maintaining employment law compliance as well as litigation avoidance.


 

 I-9 and Immigration Enforcement Bootcamp: Employer Best Practices & Compliance

 

Category: HR MGMT

This I-9 and E-Verify “Compliance Bootcamp” will give you the tools to function as a subject matter expert, develop and implement a solid compliance program, and protect your organization from potentially serious financial and reputational risk.


 

 Identify and Manage Data Integrity Issues, CSV and 21 CFR Part 11: 2-Day In-Person Seminar

 

Category: Compliance-Regulation

The FDA and other Health Authorities worldwide have focused their attention on data integrity, considering data integrity to be a significant risk to public safety.


 

 Improving Employee Accountability

 

Category: GENERAL MGMT

The buck stops here! Eliminate finger-pointing and blame-shifting ... and get people to own their jobs once and for all!


 

 Insurance Claims: Investigation and Adjuster Negotiations

 

Category: INSURANCE

Get your clients the claim settlements they deserve and build lasting working relationships with the insurance professionals you'll have to deal with for your next claim.


 

 Insurance Fraud Investigation: 2-Day Workshop

 

Category: Compliance-Regulation

Participants will have the opportunity to review the red flags that could be an indicator of insurance fraud. The procedures for conducting an insurance fraud investigation will be discussed and the legal issues will be examined.


 

 Insurance Investigation and Litigation of a Fire

 

Category: LAW - Insurance

Walk through the investigation and claim process – and gain practical insights along the way.


 

 Integration of Human Factors into Medical Device Design: FDA and European Commission - 2-Day In-person Seminar

 

Category: Compliance-Regulation

The benefits of this course include the following:Show you how Human Factors can actually decrease development time and overall product development costs.Show how to plan and execute strategic Human Factors testing cycles.


 

 Investigational New Drug (IND) & Investigational Device Exemptions (IDE) Applications Preparation and Submission, and Conducting FDA Meetings

 

Category: Compliance-Regulation

In this practical course, which is designed to help participants to acquire the knowledge and insight needed to understand and begin to construct core U.S. drug and biologics submissions, including Investigational New Drug (IND), and Investigational Device Exemptions (IDE) applications. Participants also will gain experience with tools that help manage timelines and sections needed from contributors.


 

 Laboratory, Medical and Device Performance and Validation following Regulatory and ICH Statistical Guidelines

 

Category: Compliance-Regulation

In this two day workshop seminar one will learn the different regulatory agencies expectations of the quantification and development of a sound statistical monitoring of process control that are accepted, effective, and efficient.


 

 Latest International Financial Reporting Standards (IFRS) Updates: 2-Day In-person Seminar

 

Category: Compliance-Regulation

his training course will give you an understanding of the recent issues and accounting standards which are part of International Financial Reporting Standards (IFRS) reporting. As companies enter into arrangements with their global counterparts.


 

 Linking Customer, Employee and Process Data to Drive Profitability

 

Category: MARKETING

This seminar is designed for people who want to learn how to plan, execute, and/or manage linkage research and analysis initiatives.


 

 Managing Marketing Research to Enhance Accountability and ROI

 

Category: MARKETING - Marketing Research

This seminar, designed for marketing research managers, addresses key managerial issues that impact on the effectiveness of real world marketing research.


 

 Market Research: How to Get the Right Data to Make the Right Decisions Onsite Training

 

Category: MARKETING

Improve your market research to gain a clear understanding of what your customers value—and what they’re willing to pay.


 

 Market Segmentation and Positioning Research

 

Category: MARKETING - Marketing Research

This seminar is designed to teach you how to segment your markets and select the best target markets for your products and services.


 

 Mastering International Customs - INCOTERMS, NAFTA, TPP, TAA, 19 CFR 152 and more: In-person Seminar

 

Category: Compliance-Regulation

In this one day seminar, you will learn a broad range of topics to introduce you to the areas of import trade management.


 

 Medical and Dental Practice OSHA Compliance Course

 

Category: HEALTH CARE

This one-day comprehensive training is the perfect solution to help you keep your practice safe and 100% OSHA compliant!


 

 Medical Device Architecture - Design for Safety: 2-Day In-Person Seminar

 

Category: Compliance-Regulation

This two day interactive course will also address the basic risk management methods and risk related methodologies like FMECA that significantly influence the architectural design.


 

 Medical Device Risk Management A to Z - Best Practices for Effectiveness and Efficiency

 

Category: Compliance-Regulation

The medical device risk management (ISO 14971) course will be given using an interactive workshop format taking attendees through all of the risk management activities required by ISO 14971.


 

 Medical Device Single Audit Program [MDSAP] Implementation & Participating Country Regulatory Processes: U.S., Canada, Brazil, Australia and Japan

 

Category: Compliance-Regulation

This two-day seminar is focused on understanding the Medical Device Single Audit Program, the scope of the program, how to apply, the Authorized Organizations, the rating system developed and what you can expect when signing onto the program.


 

 Medical Records Management and Legal Compliance

 

Category: HEALTH CARE

Handle critical healthcare records confidentially, efficiently, and accurately while maintaining legal compliance.


 

 Medicare Compliance: Covering All Aspects of Personal Injury Litigation for Plaintiffs and Defendants Counsel

 

Category: LAW - Medical

This engaging legal course includes in-depth discussions on mandatory insurer reporting, Medicare conditional payments, and Medicare Set-Asides.


 

 Microlaunch Marketing Research Simulation – Experiential Learning In A Competitive Environment

 

Category: MARKETING - Marketing Research

In this one-day program you will compete in teams against other seminar participants to bring a new product to market, by building upon the fundamental learning's from the 101 Practical Marketing Research course. Each group will design and commission research projects based upon allocated budgets and make decisions on: the marketing objective; the research technique, which includes time and cost parameters; the sample size needed for the research; and the input (stimulus) material to be used.


 

 Modern HIPAA Compliance - Managing Privacy, Security, and Breach Notification in a World of New Technologies, New Threats, and New Rules

 

Category: Compliance-Regulation

The HIPAA Regulations carry significant obligations to protect the privacy and security of Protected Health Information, and significant penalties in the millions of dollars can result from non-compliance.


 

 Mortgage Lending Workshop

 

Category: Compliance-Regulation

An in-depth look at the recent issuances of final regulations required under Dodd-Frank, looking into topics like qualified mortgages, the new HOEPA requirements, revised escrow rules, higher risk mortgages, and the new loan originator compensation rules.


 

 Navigating the Maze for Post-Market Compliance -- Complaint Handling, MDRs, Recalls and Proposed Guidance on FDA Risk Benefits

 

Category: Compliance-Regulation

Medical Device Reporting (MDR), and Recall compliance are critical to the continue survival of all device manufacturers.


 

 Neuroscience Toolkit for Business Decisions

 

Category: MARKETING - Marketing Research

This intensive 1.5-day workshop is designed to provide critical knowledge to evaluate, understand and interpret the application of neuroscience knowledge and tools to test content effectiveness, marketing communication, branding and customer experiences. The workshop will offer a lens into the new tools that neuroscience offers the business world which replace traditional methods for research, analytics and insight gathering.


 

 New Product Research: Laying the Foundation for New Product Success

 

Category: MARKETING - Marketing Research

In this seminar you will learn how to design and implement marketing research studies to guide the total product service development and evaluation process.


 

 Next Generation Qualitative Tools: Social Media, Online Communities & Virtual Research Platforms

 

Category: MARKETING - Marketing Research

This limited enrollment, intensive 2-day workshop is designed to educate you on the latest technology offerings and methodologies available for conducting qualitative research as well as teach you how to use it.


 

 Next Generation Quantitative Tools: Online Innovations, Mobile, Best Practices

 

Category: MARKETING - Marketing Research

During this two-day seminar, get up to date with the most recent developments relating to Web surveys and learn the when, where, why, and how about online research.


 

 Operations Risk Management and Mitigation - from Assessment to Implementation

 

Category: Compliance-Regulation

Operations Risk Management is about protecting a bank’s sustainability & long-term health. It’s about growing a bank’s revenue & increasing its reputation in the market. In short, Operations Risk Management is a value added rather than a cost center.


 

 OSHA 30-Hour Compliance Course

 

Category: SECURITY/SAFETY

Earn your 30-hour OSHA course completion card with 5 Days of in-depth training!


 

 OSHA 30-hour Outreach Training Compliance Course

 

Category: SECURITY/SAFETY

A 5-Day course for safety professionals who are serious about providing the highest level of OSHA compliance.


 

 OSHA Compliance

 

Category: SECURITY/SAFETY

Keep your workplace safe and stay fully compliant with OSHA's ever-changing regulations


 

 Packaging and Labeling in Pharmaceutical Production: 2-Day In-Person Seminar

 

Category: Compliance-Regulation

Pharmaceutical and life sciences companies are under an extreme amount of pressure to maintain an ever-increasing amount of regulation and legislation.


 

 PCI COMPLIANCE

 

Category: INTERNET - Security

Ensure that your organization is in complete compliance with the latest PCI Data Security Standards to protect your customers and your reputation


 

 Positioning Research

 

Category: MARKETING - Marketing Research

In this seminar you will learn why positioning research is important to market success and the consequence of an ill-defined positioning strategy.


 

 Practical Conjoint Analysis and Discrete Choice Modeling

 

Category: MARKETING - Marketing Research

This 2.5-day comprehensive seminar is designed to help marketing research practitioners obtain a complete understanding of conjoint analysis and discrete choice modeling, starting with the design process through utility estimation to translating results into actionable information.


 

 Practical Marketing Research

 

Category: MARKETING - Marketing Research

This seminar is designed for people who want to learn how to plan and implement marketing research studies from start to finish.


 

 Practical Multivariate Analysis

 

Category: MARKETING - Marketing Research

In this seminar you will learn how to select and interpret the best multivariate technique for analyzing the complex relationships between many variables typically encountered in marketing research studies.


 

 Pricing Research

 

Category: MARKETING - Marketing Research

This seminar will cover both traditional as well as conjoint/simulation based research methods for evaluating alternative pricing strategies.


 

 Project Management in Clinical Research

 

Category: Compliance-Regulation

This course is an integrative learning experience, combining a comprehensive review of the good clinical practice core principles and project management strategies applicable to clinical research during the new drug development process.


 

 Project management tools to improve productivity and compliance in Analytical laboratories: 2-day Workshop

 

Category: PROJECT MANAGEMENT

In this two day workshop you will learn the different tools of PM, proper mind set/expectations and sound lean lab management program skills in order to develop and implement efficient techniques.


 

 Qualitative Research with Children

 

Category: MARKETING - Marketing Research

This course is designed for marketing researchers from such industries as toys, accessories, snacks, breakfast cereals, and others who market products and services for children 6 years of age and older.


 

 Quality and GMP Compliance for Virtual Companies (Pharmaceutical, Medical Device & Biologics Industries)

 

Category: Compliance-Regulation

In this two day workshop conference you will learn the requirements and expectations of major health care regulators that are applicable to


 

 Quality Control Laboratory Compliance - cGMPs and GLPs

 

Category: Compliance-Regulation

This course will examine the fundamental requirements for all QC laboratories subject to FDA inspection, recent trends from FDA inspection reports and enforcement actions


 

 Raw Material Requirements (Health Canada/USP/EP) in a cGMP Environment - Issues and Solutions

 

Category: Compliance-Regulation

The objective of this two day seminar is to explore raw materials and their requirements – issues and solutions


 

 REACH and RoHS Compliance: Gain a Deeper Understanding

 

Category: Compliance-Regulation

This 2 day seminar will go into the specifics of the REACH and RoHS regulations, provide case studies and share lessons learned so your organization can benefit from the mistakes of others.


 

 REACH and RoHS Compliance: Protecting Revenues with Advanced Compliance

 

Category: Compliance-Regulation

REACH and RoHS have been referred to as …one of the most complex regulations in the history of the EU. Do not miss this 2 day seminar to find out why


 

 Records Retention and Destruction

 

Category: LAW

Eliminate risk and ensure compliance with the latest legal requirements


 

 Reduce costs for compliance with data integrity: 21 CFR Part 11, SaaS/Cloud, EU GDPR

 

Category: Compliance-Regulation

This highly interactive two-day course uses real life examples and explores proven techniques for reducing costs, usually by two-thirds, associated with implementing, and maintaining computer systems in regulated environments.


 

 Registration & Listing, FDA Inspection Strategies and Compliance Initiatives - Medical Device. - By Compliance Global Inc.

 

Category: Compliance-Regulation

webinar on FDA Inspection Strategies and how they reach decisions in developing inspection and compliance plans. Registration and how FDA uses this data will be discussed


 

 Roadmap of California Medical Leaves - Ultimate Guide to PDL, FMLA, FEHA, SDI, CFRA, PFL, ADA and Workers Compensation and Handling Performance Management Challenges

 

Category: Compliance-Regulation

The seminar will focus on how California leaves such as FEHA and CFRA interact with Federal medical leaves, such as the FMLA and ADA.


 

 Roadmap to Advanced Human Resources and Employment Law Essentials

 

Category: Compliance-Regulation

Are you prepared to protect your organization? The average lawsuit is $165,000 without lawyer fees. If the case goes to trial it could cost $1,000,000 or more! Also, non-compliance of employment laws can land you in jail. Be prepared!


 

 Roadmap to Human Resources and Employment Law Essentials: 3-Day In-person Seminar

 

Category: HR MGMT

Attendees in this seminar will address the legal consequences of human resource decision making, as well as, the managerial significance of federal regulations and applicable state laws.


 

 Robust Quality System Approach to Pharmaceutical Products: Scientific Basis and Implementation of Current Regulations

 

Category: Compliance-Regulation

This course will provide an overview of some relevant rules and regulations concerning their scientific basis, development and interpretation.


 

 Sales and Use Tax - Compliance and Best Practices

 

Category: Compliance-Regulation

Sales and Use Tax Compliance is among the most challenging areas for Accounts Payable professionals to master. Currently, 45 states and the District of Columbia levy a sales and use tax.


 

 Secrets for Writing Excellent SOPs (Standard Operating Procedures) Webinar

 

Category: Compliance-Regulation

Standard Operating Procedures (SOPs) are a critical ingredient in an effective and efficient Quality Management System. SOPs are typically one of the first things an investigator asks for in an inspection. Well written SOPs send a message to the FDA and Notified Bodies that your QMS is complete, accurate, and followed. More importantly, well written SOPs ensure that your personnel can consistently and accurately follow your processes resulting in correct outcomes and quality work. This webinar will help you structure your QMS and develop accurate, clear, unambiguous SOPs.


 

 Seminar on 21 CFR Part 11 Compliance for Computer Systems Regulated by FDA

 

Category: Compliance-Regulation


 

 Seminar on 21 CFR Part 11 compliance for software validation and SaaS/Cloud

 

Category: Compliance-Regulation

This interactive two-day course explores proven techniques for reducing costs associated with implementing, using, and maintaining computer systems in regulated environments.


 

 Seminar on Applied Statistics, with Emphasis on Risk Management in R&D, QA/QC, and Manufacturing

 

Category: Compliance-Regulation

The 2-day seminar explains how to apply statistics to manage risk in R&D, QA/QC, and Manufacturing, with examples derived mainly from the medical device design/manufacturing industry.


 

 Seminar on Applying ISO14971 and IEC62304 - A guide to practical Risk Management

 

Category: Compliance-Regulation

This course will introduce all necessary steps to design, implement and test critical medical devices in a regulatory compliant environment. This course will additionally address the software risk management and the resulting interfaces to device level risk management.


 

 Seminar on Applying U.S. FDA Laws and Regulations to Each Phase of Total Product Life Cycle (TPLC)

 

Category: MEDICINE/NURSING

This workshop style training course is supported by comprehensive knowledge of U.S. FDA laws and regulations and 30 year of extensive experience working within in the U.S. FDA regulated industries.


 

 Seminar on Audit Like the FDA - What you need to know for a truly effective internal audit program

 

Category: Compliance-Regulation

This 2 day seminar will explore how to create and implement an efficient and effective internal audit program. Internal Audit is a required part of an effective quality system. More importantly, it is an incredibly powerful tool to identify areas of non-compliance.


 

 Seminar on Auditing Analytical Laboratories for FDA Compliance

 

Category: Compliance-Regulation


 

 Seminar on Biostatistics for the Non-Statistician

 

Category: Compliance-Regulation


 

 Seminar on Clinical Research for Cardiovascular Pharmaceuticals: Ensuring Compliance of Traditional and New Cardiovascular Medications

 

Category: Compliance-Regulation

Understanding basic clinical research requires excellent people and project management skills, and very good scientific writing and organization skills. Also paramount is gathering necessary information to manage the statistical analysis and data management of all the many clinical studies. The clinical development plans must be laid by experienced leaders and project managers.


 

 Seminar on Combination Products

 

Category: MEDICINE/NURSING

Combination products are especially challenging to register and maintain since they consist of two or more regulated components covered by different and usually independent sets of regulations in both the EU and US and various other regions.


 

 Seminar on Combination Products Regulations: Drug and Device Combinations in the USA and EU

 

Category: Compliance-Regulation


 

 Seminar on Complaints, Adverse Event Reporting, and Recalls - An Integrated Approach

 

Category: MANUFACTURING/OPERATIONS - QC/QA

This workshop covers these primary and secondary QMS processes and analyzes them in terms of US, EU, and Canadian regulations.


 

 Seminar on Complete 1099, TIN Matching, B-Notice, FATCA and Non-resident Alien 1042-S Compliance Update

 

Category: FINANCE/INVESTING - International Finance & Taxation


 

 Seminar on Compliance Boot Camp

 

Category: Compliance-Regulation

Course


 

 Seminar on Conducting Internal Investigations

 

Category: HR MGMT - Employee Problems/Special Employees

How you handle internal complaints can make all the difference of whether an employee goes externally with their complaints.


 

 Seminar on Construction: OSHA Construction Hazards for any Jobsite

 

Category: LAW - Construction

How to train staff to have the correct documentation in place. Ensure that the organization keeps documentation updated and realistic.


 

 Seminar on Data Integrity - Beyond 21 CFR 11 & Annex 11

 

Category: Compliance-Regulation

This course is appropriate for beginner and experienced person alike. The topics will build on each other and will give you the latest trends in our heavily regulated industry and how to make it easy for yourself while still achieving data integrity.


 

 Seminar on Developing Technical Training in the Life Sciences

 

Category: Compliance-Regulation

Developing Technical Training in the Life Sciences is a 2-day seminar that addresses the unique challenges of developing and managing training in Life Sciences companies. The Life Sciences pose unique challenges to training developers.


 

 Seminar on Drug dissolution testing and establishing plasma drug levels in humans

 

Category: LAW - Health Care


 

 Seminar on Effective Internal and External Quality Assurance Auditing for FDA Regulated Industry

 

Category: Compliance-Regulation

This seminar will provide an overview and in-depth snapshot and a refresh of internal and external auditing. Those interested in how to prepare for a QA audit and how to enhance their internal/external quality audit system as a valuable regulatory compliance tool will also benefit from this course.


 

 Seminar on FDA Device Software Regulation

 

Category: LAW - Environmental Law

Software's level of complexity and use is expanding at exponential levels. Likewise the potential risks to health follow suit. Problems with software create a number of different hurdles.


 

 Seminar on FDA's GMP Expectations for Phase I and First-in-Man Clinical Trials

 

Category: Compliance-Regulation

To gain an understanding of the requirements for advancing drugs from research into early clinical development and the minimum FDA requirements for phase I GMPs. To learn practical applications for implementing phase I manufacturing strategies to meet FDA requirements.


 

 Seminar on Food Safety and Defense: Key Factors to Safely Manufacture, Package and Handle Food Products

 

Category: FOOD INDUSTRY

This Seminar will focus on Food Defense & will detail what an organization needs to have in place in order to safely manufacture, package, & or handle food products. It will cover a broad range of: production types, facilities, & transportation of goods.


 

 Seminar on Fundamental Laboratory Record Keeping and Compliance Issue

 

Category: Compliance-Regulation

This seminar will go through many of the compliance areas and point out some of both types. IF or those implementing GLP or striving to maintain certification, this course should point out many areas to cover that would lessen an unsatisfactory audit.


 

 Seminar on Geological Exploration 2016

 

Category: EDUCATION/TRAINING

We will introduce you to an effective and affordable methodology that identifies prospective targets which are related to, or controlled by tectonic structures.


 

 Seminar on HIPAA - Putting an Organizational Compliance Program in Place

 

Category: HEALTH CARE

This starts with the fundamentals of a HIPAA compliance program.If your healthcare practice, business, or organization needs to understand how to put HIPAA compliance program in place or make sure the current program is adequate and can withstand government scrutiny, please join us for this informative and interactive 2 day training course.


 

 Seminar on HIPAA - Understanding Compliance Program Requirements

 

Category: HEALTH CARE

Attendees will leave the course clearly understanding of all the requirements for a comprehensive HIPAA compliance program and what steps need to be taken to mitigate risk.


 

 Seminar on HIPAA Compliance for Small Healthcare Providers

 

Category: HEALTH CARE

If your small healthcare practice needs to understand how to put a HIPAA compliance program in place or make sure the current program is adequate and can withstand government scrutiny, please join us for this informative and interactive Two-day training course.


 

 Seminar on HIPAA Privacy, Security and Breach Notification Compliance: Understanding the Requirements, Preventing Incidents, Surviving Audits, and Avoiding Penalties

 

Category: HEALTH CARE

This session is designed to provide intensive, two-day training in HIPAA compliance, including what's new in the regulations, what's changed recently, and what needs to be addressed for compliance by covered entities and business associates.


 

 Seminar on HIPAA Security & Privacy Official - Roles and Responsibilities

 

Category: HEALTH CARE

This seminar will cover reviews, creation, and amending policy and procedure. After completing this course, a HIPAA Security and Privacy Official will have a clear understanding for what needs to be place when it comes to all of the HIPAA regulations.


 

 Seminar on HIPAA Upcoming Changes

 

Category: HEALTH CARE

In addition, this course will cover the highest risk factors for being sued for wrongful disclosures of PHI and the manner in which patients are now using state laws to sue for wrongful disclosures.


 

 Seminar on Human Factors and Predicate Combination Products

 

Category: Compliance-Regulation

This seminar will compare these Guidance documents. Additionally, strategic recommendations will be presented on how to implement these requirements into the medical device design, development and approval processes. Finally, Human Factors methods and best practices will be covered that the FDA is requiring.


 

 Seminar on Human Subjects Research Seminar: Current Regulations under FDA and HIPAA

 

Category: Compliance-Regulation

This two day seminar will provide the foundation for the application, concepts and theories of clinical research. Within the two days, attendees will learn about the historical evolution of research, current regulations and guidelines including the Common Rule, FDA regulations and HIPAA.


 

 Seminar on Incorporating Risk Management into Your HR Policy

 

Category: HR MGMT

This workshop reviews the current risk management risks, discusses the use of HR audits and HR audit techniques, and analyzes how HR audits can be used to help organizations reduce risks and seize potential opportunities.


 

 Seminar on Japan - Regulatory Filing Requirements and Compliance Processes for Medical Devices - Singapore

 

Category: Compliance-Regulation


 

 Seminar on Marketing Products Without Getting Hammered by FDA

 

Category: Compliance-Regulation

Most importantly, you will understand the boundaries that FDA uses and how easy it is to cross them. With information from this course, you can step back and rationally evaluate your firm's regulatory profile for advertising and promotion.


 

 Seminar on Master HIPAA Compliance in Six Steps

 

Category: HEALTH CARE

In this seminar Paul Hales will capture your attention with visual presentations, discussion and learning exercises and show how to find the right rule with the step-by-step procedures you need when you need them.


 

 Seminar on Modern HIPAA Compliance - Managing Privacy, Security, and Breach Notification in a World of New Technologies, New Threats, and New Rules 2017

 

Category: HEALTH CARE

The HIPAA Regulations carry significant obligations to protect the privacy and security of Protected Health Information, and significant penalties in the millions of dollars can result from non-compliance.


 

 Seminar on Onsite GCP Review and Update including the all-important 'Investigators Responsibility'

 

Category: Compliance-Regulation


 

 Seminar on Overview of Device Regulation - FDA

 

Category: Compliance-Regulation

This course provides a basic description of an FDA regulatory strategy for medical devices and explains the relationships between regulatory strategy and product development. It offers guidelines for developing successful strategies for medical devices


 

 Seminar on Product Information for Medicinal Products in the EU

 

Category: MEDICINE/NURSING


 

 Seminar on QC Laboratory Compliance and Meeting FDA Requirements

 

Category: Compliance-Regulation

This two-day course is designed for all persons who work in, supervise, or are involved in the management of pharmaceutical and medical device Quality Control laboratories.


 

 Seminar on Quality by Design - Essential Techniques for Medical Devices

 

Category: MEDICINE/NURSING

In this seminar, we will cover Design Controls for medical devices. We will understand the requirements for design controls and how to translate them into an efficient and effective process for your company.


 

 Seminar on Texting and E-mail with Patients: Patient Requests and Complying with HIPAA

 

Category: HEALTH CARE

The session will be valuable for both newcomers to HIPAA compliance as well as seasoned veterans. HIPAA compliance will be explained and discussed in detail, from the basics through the latest changes and new technology issues, so that the attendee will have a coherent understanding of not only the rules, but also how to think about compliance and make sound compliance decisions on a day-to-day basis in the context of mobile devices.


 

 Seminar on The A to Z's of HIPAA Privacy, Security, and Breach Notification Rules

 

Category: HEALTH CARE

This session is designed to provide intensive, two-day training in HIPAA compliance, including what's new in the regulations, what's changed recently, and what needs to be addressed for compliance by covered entities and business associates.


 

 Seminar on The A to Z's of Writing and Enforcing Effective SOPs

 

Category: Compliance-Regulation

This session will address recent enforcement actions for SOP related violations but no surprise. Most of our enforcement actions are documentation related, i.e., SOP or other procedural documents. We will review examples from warning letters and then review the good and bad SOPs and templates. Standard operating procedures work best when they are designed to achieve specific results.


 

 Seminar on the Complete Payroll Law

 

Category: FINANCE/INVESTING

Learn where to find the authoritative rules to support your policies and procedures. Accelerate your learning using our organized and thoughtful delivery and determine to handle your role with confidence.


 

 Seminar on The EU Clinical Trial Regulation + EU Filings & Registrations

 

Category: Compliance-Regulation


 

 Seminar on U.S. Payments Industry: The Players, Trends, and Compliance Issues Faced

 

Category: ACCOUNTING - Payroll

The role of the compliance officer is changing because banks and corporations are struggling to serve many masters; some with similar goals and others with contradictory ones. Regulators, corporate clients, Boards of Directors, and shareholders are pulling them in their own directions.


 

 Seminar on Validating Radiation Sterilization for Medical Products

 

Category: MEDICINE/NURSING

Learn how to plan for post radiation resistance and lifetime functionality. All radiation modalities (gamma, e-beam, x-ray) will be reviewed for a basic understanding of the sterilization process and the influences that product design and assembly can have on success.


 

 Seminar on Validation and 21 CFR 11 Compliance of Computer Systems: Intermediate to Advanced

 

Category: Compliance-Regulation

Computer Systems Validation (CSV) also known as Software Validation is all-pervasive in the Life Sciences Industry. It is a requirement of all the predicate rules, as well as 21 CFR 11 and Annex 11. However, unless one knows how to implement CSV, it is often very hard to detect the requirement for CSV, and very hard to determine what needs to be done, to meet domestic and / or international regulations or business continuity requirements. In addition, the FDA has stepped up 21 CFR 11 inspections that include CSV.


 

 Seminar on Validation and Part 11 Compliance of Computer Systems and Data

 

Category: Compliance-Regulation

This 2-day interactive course provides the regulatory background and guides attendees through the complete equipment qualification and computer system validation processes from planning to reporting.


 

 Seminar on What to Expect in a Federal HIPAA Audit & How to Avoid Audit

 

Category: HEALTH CARE

This lesson will be addressing how practice/business managers (or compliance offers) need to get their HIPAA house in order before the imminent audits occur. It will also address major changes under the Omnibus Rule and any other applicable updates for 2017.


 

 Shopper Marketing: Insights, Innovation & Implementation

 

Category: MARKETING - Marketing Research

The focus of this two-day seminar is to provide a foundation and framework for developing a strong shopper marketing discipline and shopper insights program to support it.


 

 SOP Writing, Training and Compliance in the Pharmaceutical Industry

 

Category: Compliance-Regulation

This course will also show you how to perform ongoing assessments of learners’ retention of knowledge of SOP content for continuous improvement and avoidance of procedural deviations, using the tools already available in your company’s training software.


 

 Supplier Quality Agreements - Essential for suppliers of most outsourced processes

 

Category: Compliance-Regulation

This presentation will provide an understanding of what the current guidance documents suggest you include in supplier agreements.


 

 Technical Project Management

 

Category: PROJECT MANAGEMENT

Integrate technical disciplines with project management skills to meet your business requirements!


 

 The 30-Hour California OSHA Compliance Course

 

Category: SECURITY/SAFETY

If you're serious about Cal OSHA and safety training - and knowing all the benefits that come with it for you and your organization - this is the one course you can't afford to miss.


 

 The 30-Hour OSHA Compliance Course

 

Category: SECURITY/SAFETY

If you're serious about OSHA and safety training-and knowing all the benefits that come with it for you and your orgnization-this is the one course you can't afford to miss.


 

 The A to Z's of Microbial Control, Monitoring and Validation of Water Systems for Pharmaceuticals, Biologics, Medical Devices, Cosmetics, and Personal Care Products

 

Category: Compliance-Regulation

This course is designed to provide a microbiology-focused education about all aspects of water systems and how biofilm manages to thrive there. Prior microbiological education or training, though a plus, is not a requirement


 

 The Challenges of an Effective Change Control Program and How to Address OOS Results

 

Category: Compliance-Regulation

In addition, the seminar will also highlight some of the benefits that a well maintained change control program provides to a company along with reviewing when change control is not required.


 

 The Conference on OSHA Compliance

 

Category: SECURITY/SAFETY

What OSHA compliance issues you must know


 

 The Essentials of OSHA Compliance

 

Category: SECURITY/SAFETY

A comprehensive 2-day update in workplace safety issues and the latest OSHA regulations


 

 The Essentials of Wage & Hour Law

 

Category: HR MGMT

How to protect your organization, avoid violations and penalties, and remain in compliance with the FLSA.


 

 The Improving Employee Accountability Seminar

 

Category: GENERAL MGMT

The Improving Employee Accountability Seminar


 

 The Internal Audit Function

 

Category: Compliance-Regulation

The session will also highlight many of the challenges outlined in Ms. Fountain's book on Leading the Internal Audit function. These challenges will help internal auditors and management understand alternatives approaches to coming to an acceptable answer


 

 The Regulations of OTC Drugs

 

Category: Compliance-Regulation

This course on FDA regulation of OTC drug products is intended to provide attendees with the knowledge and skills needed to develop and produce an OTC Drug Product for marketing and sale in the U.S.


 

 The Ultimate Course in Payroll Management

 

Category: ACCOUNTING - Payroll

The first step to complying with regulations is understanding them. That's why you'll begin your day with a crash course in payroll's legal basics. You'll find out what areas fall under state, federal, and joint regulation, and learn how to avoid the often staggering penalties and fines of non-compliance.


 

 The Veterinary Drug Approval Process and FDA Regulatory Oversight

 

Category: Compliance-Regulation

This seminar on veterinary medicine regulations will provide attendees with a comprehensive understanding of FDA’s veterinary drug approval process


 

 Tools and Techniques of Data Analysis

 

Category: MARKETING - Marketing Research

This intensive seminar uses a step by step procedure composed of several decision flow charts to help you select and implement the correct statistical techniques for your problems.


 

 Upselling Without Fear: Locking Customers Into Your Products Webinar

 

Category: SALES/CUSTOMER SERVICE

You’ll learn how to overcome upsell apprehension, what drives customers to buy, and powerful techniques and phrases to close the sale.


 

 US and Canada Customs Brokerage - A Thorough Analysis: 2-Day In-person Seminar

 

Category: Compliance-Regulation

This course will talk about US/Canadian Customs Brokerage.What does a broker do?How can I be sure that all of my legal and regulatory requirements are met?What would I need to cover if I brought brokerage in-house?


 

 US GCP Fundamentals for Pharmaceutical and Biologic Companies

 

Category: Compliance-Regulation

This seminar provides an introduction to GCP, with emphasis on the regulations governing drug and biologic clinical trials. (Most of the information is also applicable to medical devices, but specific requirements for device trials are not discussed.)


 

 US Good Clinical Practice (GCP) Regulations and ICH GCP Guidelines

 

Category: Compliance-Regulation

This program will emphasize FDA's GCP requirements for human use pharmaceutical and biologic drug products.


 

 US Immigration Compliance Training & Defense Strategies in the TRUMP Era

 

Category: Compliance-Regulation

This course will examine the regulatory compliance requirements governing the employment and utilization of H-1B, L-1, F-1/OPT/STEM, and B-1 visa holders from the perspective of U.S. enforcement authorities.


 

 Using The Internet in Your Legal Practice: Free Online Research and More

 

Category: LAW - Legal Research

Join us for an engaging day of internet exploration. Discover new research resources. Get tips from an IT professional on protecting yourself and your firm while using the internet.


 

 Validation and Part 11 Compliance of Computer Systems and Data

 

Category: Compliance-Regulation

Analytical and other equipment should be qualified and computer systems should be validated to demonstrate suitability for the intended use.


 

 Validation, Verification and Transfer of Analytical Methods (Understanding and implementing guidelines from FDA/EMA, USP and ICH)

 

Category: Compliance-Regulation

This 2-day workshop will give attendees the background to understand the requirements, and even more significantly, it will focus on strategies and provide tools to implement most critical requirements.


 

 Wage and Hour Law Under the FLSA: 2-Day In-person Seminar

 

Category: EMPLOYMENT LAW

The Fair Labor Standards Act (FLSA) applies to virtually all public and private employers, and is chock- full of rules about everything from the minimum wage to overtime pay. Along with these rules come exceptions and exemptions.


 

 Wage and Hour Law: The Essential One-day FLSA Update

 

Category: HR MGMT

Avoid violations, penalties and legal hassles with the most current, concise training on employee classification, record keeping and FLSA compliance


 

 Workplace Safety and OSHA Compliance

 

Category: SECURITY/SAFETY

An intensive one-day update on the latest OSHA rules and regulations, plus critical training on key safety issues for your organization


 

 Workplace Safety and OSHA Compliance for Health Care Industry

 

Category: SECURITY/SAFETY

The one-day comprehensive OSHA course that covers the unique challenges found in the medical field


 

 World Class Risk Management - What The Best International Standards Say About Risk - ISO 31000, ISO 14971 and ICH Q9

 

Category: Compliance-Regulation

Are you a Supervisor, Manager, or Director with risk management responsibilities? Do you have questions about what you are doing and why? If the answer is “yes,’ then this is the right course for you!


 

 Writing and Presenting Marketing Research Reports

 

Category: MARKETING - Marketing Research

In this seminar you will learn how to create action standards/research objectives and how to write and present marketing research reports that are responsive to management needs.


 
 

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