GDPR Healthcare general data protection regulation GDPR compliance HIPAA privacy security breach notification requirements training seminars workshops and conferences in AA

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Your search for 'GDPR Healthcare general data protection regulation GDPR compliance HIPAA privacy security breach notification requirements' training seminars workshops and conferences in US and Canada has produced the following results.

 2015 HIPAA Changes: Get Updated on the Issues and Risks for Renewed Audit Efforts - By Compliance Global Inc.

 

Category: HEALTH CARE

Training Provider: Compliance Global

Webinar on 2015 HIPAA Changes will be addressing the major changes under the Omnibus Rule changes and other applicable updates for 2015

      
 

 2018 HMDA Bank and Reportable Transaction Coverage Requirements

 

Category: Compliance-Regulation

Training Provider: Online Compliance Panel

Under the leadership of the Consumer Financial Protection Bureau the rules change significantly in 2017, 2018, and for large institutions again in 2020. There will be changes reducing the number of financial institutions must report, the types of loans subject to reporting, the data which will have to be reported and the methods and IT reporting requirements.

      
 

 Aseptic Processing Overview and Validation: 2-Day In-Person Seminar

 

Category: Compliance-Regulation

Training Provider: ComplianceOnline

This course will provide an overview of the requirements for aseptic and bulk manufacturing operations, including facility design, contamination controls and acceptable personnel behaviors.

      
 

 Child Support Garnishment Webinar

 

Category: Compliance-Regulation

Training Provider: Online Compliance Panel

Learn the requirements to effectively handle garnishment orders and withholding, Federal and state requirements, specific issues.

      
 

 Design Reviews and Design Controls to meet FDA Requirements Webinar

 

Category: Compliance-Regulation

Training Provider: Online Compliance Panel

Attend this webinar to learn the objectives of having design controls in medical device manufacturing, and elements of design controls.

      
 

 Developing a Customs Compliance Program under the Reasonable Care Standard Webinar

 

Category: Compliance-Regulation

Training Provider: Online Compliance Panel

This training program will help participants create a customs compliance program using the Reasonable Care Standard. If you already have a program, this webinar will help benchmark to the acceptable standard. What passes for reasonable care is not always the same for imports and exports. This program will help you meet those standards.

      
 

 DFS New Cyber Requirements for Financial Organizations and Insurance Companies Webinar

 

Category: Compliance-Regulation

Training Provider: Online Compliance Panel

On September 13, 2016, the New York State Department of Financial Services published draft regulations addressing Cybersecurity and related business continuity issues for over 3,000 regulated entities in the state. On Dec 28, 2016, DFS came out with revisions. These regulations for Financial Institutions and Insurance companies, is just as pertinent to all organization who wish to have resiliency.

      
 

 DMF under GDUFA - Drug Master Files: New Requirements under GDUFA Webinar

 

Category: MEDICINE/NURSING

Training Provider: Online Compliance Panel

The Generic Drug User Fee Amendments of 2012 (GDUFA) enables FDA to assess user fees and bring greater predictability to the review of generic drug applications. The law requires industry to pay user fees to supplement the costs of reviewing generic drug applications and inspecting facilities

      
 

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

 

Category: Compliance-Regulation

Training Provider: ComplianceOnline

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

Training Provider: ComplianceOnline

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

      
 

 FDA Regulations for Marketing OTC Drugs in the U.S. - By Compliance Global Inc.

 

Category: Compliance-Regulation

Training Provider: Compliance Global

Webinar on OTC Drugs in the U.S. will offer an overview of FDA requirements for marketing, labelling and promotion of OTC drugs in the U.S

      
 

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

 

Category: Compliance-Regulation

Training Provider: ComplianceOnline

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

      
 

 FDA's New Import Program for 2019 - Strict Precision

 

Category: Compliance-Regulation

Training Provider: ComplianceOnline

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

      
 

 FLSA Compensable & Overtime Rules: FLSA Requirements Webinar

 

Category: Compliance-Regulation

Training Provider: Online Compliance Panel

The session will explain the compensable and overtime calculation rules step-by-step and give examples of both the problems employers face and offer practical solutions that will keep you in compliance with the FLSA overtime and compensable time requirements.

      
 

 Food Labelling : A Practical Guide for Unambiguous Labelling Information & Compliance with Regulatory Requirements Webinar

 

Category: FOOD INDUSTRY

Training Provider: Online Compliance Panel

The fundamental rule for food and drinks labelling states that labelling must not mislead consumers. This applies to the entire label, encompassing pictures, graphics and text.

      
 

 Good Documentation Practices Webinar

 

Category: Compliance-Regulation

Training Provider: Online Compliance Panel

This webinar will cover the basics of what good documentation practices include, along with examples of practices not acceptable to auditors. This webinar will help attendees review their own procedures and what should be included in applicable training sessions for new employees along with refresher training for those who are more experienced.

      
 

 Handling BSA/AML Requirements when doing Business with Marijuana Customers Webinar

 

Category: Compliance-Regulation

Training Provider: Online Compliance Panel

Get trained on how to handle BSA#47;AML requirements when doing business with marijuana customers.

      
 

 Health Care Reform and Review of Affordable Care Act Requirements - By Compliance Global Inc.

 

Category: ACCOUNTING

Training Provider: Compliance Global

online training on Affordable Care Act Requirements for Get an accurate review of the new 1094 and 1095 tax forms, Section 6055 and 6056 reporting requirements

      
 

 HIPAA Training: Enforcing Protection for PHI & ePHI - All that you need to know. Webinar - By Compliance Global Inc.

 

Category: HR MGMT

Training Provider: Compliance Global

online training on Protection for PHI & ePHI gains significance, following stringent penalties for breaches, making understanding of new notifications imminent

      
 

 How to Satisfy OSHA Requirements and ADA Obligations 101 Webinar

 

Category: Compliance-Regulation

Training Provider: Online Compliance Panel

Implement an Effective Return to Work Program Accommodating ADA and OSHA Requirements.

      
 

 IRS Form 1099: New Requirements!

 

Category: ACCOUNTING

Training Provider: NBI Inc.

Get brought up to date with new 1099 reporting requirements, current issues and pitfalls.

      
 

 Latin America: Regulatory Compliance Requirements for Life Science Products (Focus: Brazil, Mexico, Argentina)

 

Category: Compliance-Regulation

Training Provider: ComplianceOnline

This course specifically focuses on the overall regulatory compliance requirements and procedures for Pharmaceuticals, Medical Devices, Biologics and Combination Products in Latin America

      
 

 Managing Client Expectations Without Losing Your Shirt or the Next Job - By Compliance Global Inc.

 

Category: PROJECT MANAGEMENT

Training Provider: Compliance Global

Managing client expectations and ensuring client satisfaction through soft skills.

      
 

 Medical Device Reporting Requirements for Manufacturers Final Guidance

 

Category: Compliance-Regulation

Training Provider: Online Compliance Panel

This webinar explains the MDR regulation considering the new information contained in the Guidance and describes a compliant MDR procedure. Areas covered will include death, injury and mal-function reporting requirements, record keeping requirements, report timing, clarification of the term ‘becoming aware’ and clarification of reporting using electronic form 3500A.

      
 

 Navigating the maze of changes with Form 5500 Webinar

 

Category: Compliance-Regulation

Training Provider: Online Compliance Panel

Attend this upcoming video conference and understand the basic filing requirements of Form 5500 and the recent regulatory changes.

      
 

 New GS1 US Guideline - Pharmaceutical Industry Prepares for DSCSA Item-Level Traceability Requirements Webinar

 

Category: Compliance-Regulation

Training Provider: Online Compliance Panel

New provisions of the 2013 Drug Supply Chain Security Act (DSCSA) will come into effect in 2023. The industry is using the newly updated GS1 Guideline to update their systems to comply with the law. There are many new features in the guideline that need to be understood before making changes to existing systems. This webinar will review new materials in the guideline and help you prepare to comply with the 2023 requirements. There are additional requirements that have yet to be decided within the industry that you need to be aware of and follow as they are resolved by industry and the FDA.

      
 

 Overview of the Mexican Labeling Standards and the New Labeling Requirements Webinar

 

Category: Compliance-Regulation

Training Provider: Online Compliance Panel

In this 90 minutes session, attendees will learn the Mexican labeling standard as well as and the new requirements regarding the use of Front of Pack icons and the voluntary nutritional quality seal. The regulation has been amended; the most significant change with the new regulations is the mandate to include an FOP nutrition label with information icons on saturated fat, other fat, sugar, sodium, and energy as a percentage of daily nutrients. Family packs (including cheeses of 90g or more) need a sixth icon of energy per pack. This regulation is effective from July 2015.

      
 

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

 

Category: Compliance-Regulation

Training Provider: ComplianceOnline

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

      
 

 Quality Control Laboratory Compliance - cGMPs and GLPs

 

Category: Compliance-Regulation

Training Provider: ComplianceOnline

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

      
 

 Quarterly 941 & How to be Compliant in 2016 Webinar

 

Category: Compliance-Regulation

Training Provider: Online Compliance Panel

The form 941 is an essential form for all employers that pay employees and withhold federal and FICA (social security and Medicare) taxation. In recent years several changes to the 941 form has made it difficult to understand. The importance of reconciliation and completion of not only the Form 941 but Schedule B is becoming increasingly important for employers to avoid costly disputes with the IRS resulting in penalty and interest.

      
 

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

 

Category: Compliance-Regulation

Training Provider: ComplianceOnline

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

      
 

 SOPs for FDA-Regulated Industry: Best Practices to Withstand FDA Expectations

 

Category: Compliance-Regulation

Training Provider: ComplianceOnline

This two day In-person seminar will provide step by step instructions to create SOPs for FDA-regulated organizations.

      
 

 Sterile Filtration of Pharmaceutical Products - Validation and Regulatory Requirements Webinar

 

Category: MEDICINE/NURSING

Training Provider: Online Compliance Panel

It is important that the sterile filtration process is fully understood and properly validated for your particular application. The process requirements and validation needs to differ based on the filtration requirement.

      
 

 Supplier Quality Management: Streamline your Supply Chain - By Compliance Global Inc.

 

Category: EDUCATION/TRAINING

Training Provider: Compliance Global

Webinar On Supplier Quality Management that will satisfy the FDA’s requirements and will provide the information and tools to develop

      
 

 The Best Way to Develop or Improve a Master Validation Plan - By Compliance Global Inc.

 

Category: Compliance-Regulation

Training Provider: Compliance Global

Training On Master Validation Plan for U.S. FDA CGMP, ICH Q-series, and ISO 13485 expectations and requirements

      
 

 The Importance of HR Documentation and Notice Requirements Webinar

 

Category: Compliance-Regulation

Training Provider: Online Compliance Panel

Documenting events is a crucial task, and in some cases not documenting them can lead to grim consequences. For example, did you know that not keeping track of employee's hours is fatal to overtime cases? Sometimes you might be documenting items, but focusing on the wrong items. In this training program, the webinar instructor will discuss what needs to be documented and what should be documented that strengthens employers' defenses in the event lawsuits are filed.

      
 

 Trends in Environmental, Health and Safety (EHS) rules, requirements; stay ahead of regulatory challenges

 

Category: Compliance-Regulation

Training Provider: Online Compliance Panel

TRENDS FOR THE ENVIRONMENT/EPA-- Over the years EPA has continued to create regulations; now approaching 90% of the almost 30,000 pages of federal regulatory requirements. This is not expected to continue. How the new president and his administration will affect regulations in place and in the pipeline is still unclear at this time.TRENDS FOR HEALTH AND SAFETY/OSHA-- OSHA is a smaller agency than EPA and focuses on enforcement. As with EPA, the challenges and opportunities for OSHA remain unknown.

      
 

 Unique Device Identifier (UDI) Implementation - By Compliance Global Inc.

 

Category: Compliance-Regulation

Training Provider: Compliance Global

This webinar on Unique Device Identifier (UDI) requirements will discuss the new rules implemented by FDA. You will learn the UDI elements, where it should be placed (on device, label, labeling and package, and configurations), and the GUDID data requirements.

      
 

 Valuable tools and tips for Form I-9 Audit Compliance. - By Compliance Global Inc.

 

Category: ACCOUNTING - Auditing

Training Provider: Compliance Global

Webinar on I-9 Audit Compliance to help keep you up to date on I-9 compliance and give tools on how to keep up with current I-9 requirements and changes

      
 

 What Hiring and Recruiting Trends Affect Recruitment Process? Trends and Legal Requirements

 

Category: HR MGMT

Training Provider: Online Compliance Panel

Recruitment is the process of finding candidates, reviewing applicant credentials, screening potential employees and selecting employees for an organization. Recruiting top talent can be tough for employers, especially when hiring for high demand industries or professions. Recruitment methods should ensure engaged competent, productive employees who are loyal to your organization.Effective recruitment results in an organization hiring employees who are skilled, experienced, and good fits with your corporate culture. Staying on top of the trends in recruiting and hiring employees is crucial as you compete for the best talent in the upcoming years. Government regulations, industry standards, and effective recruiting and hiring steps and techniques must remain foremost when you hire an employee.

      
 

 What the DOL New Overtime Rules Mean to Your Organization Webinar

 

Category: Compliance-Regulation

Training Provider: Online Compliance Panel

There is a lot of concern (and confusion) among employers about the new overtime regulations and what it means to their organizations. Without a doubt, the workplace is going to look a lot different in 2017. Employers will have to make decisions about whether to increase salary levels of exempt individuals or consider individuals previously considered to be exempt now non-exempt and thus entitled to overtime pay. As employers work through these thorny issues, litigation is certain to arise as to the meaning of the regulations and your employees’ attorneys are just waiting on you to make a misstep.

      
 

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