implementing change controls quality systems training seminars workshops and conferences in AA

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Your search for 'implementing change controls quality systems' training seminars workshops and conferences in US and Canada has produced the following results.

 21 CFR Part 11 Electronic Records/Electronic Signature and FDA-Regulated Computer Systems Webinar

 

Category: Compliance-Regulation

Training Provider: Online Compliance Panel

This course is intended to provide specific guidelines for coaching attendees in the concepts of 21 CFR Part 11, namely the FDA requirements for using electronic records and electronic signatures (ER/ES), and the best practices for implementing these technologies in a regulated environment.

      
 

 A Fresh Approach to Controlled Document System using Principles of Lean Documents and Lean Configuration. - By Compliance Global Inc.

 

Category: MANUFACTURING/OPERATIONS

Training Provider: Compliance Global

Webinar on Principles of Lean Documents approach to controlled document systems, based on solid principles and proven practices, by applying the Theory of Lean documents

      
 

 AP & Payroll working together for success - By Compliance Global Inc.

 

Category: ACCOUNTING - Payroll

Training Provider: Compliance Global

This webinar will give you insight on best practices for AP & Payroll to work together to achieve the shared goal of compliance for your company. Payroll is considered both a human resources and a financial management function & payroll professionals need to interact with the AP department

      
 

 Applying Computer System Validation to Mobile Applications Webinar

 

Category: Compliance-Regulation

Training Provider: Online Compliance Panel

Learn how computer system validation can be applied to mobile applications subject to FDA regulations, what are the best practices, trends in validation.

      
 

 Clinical Trial Site Quality Management System Webinar

 

Category: Compliance-Regulation

Training Provider: Online Compliance Panel

Attend this webinar to understand the key components of a QMS, key elements of a document management program, critical aspects of a training program, more.

      
 

 Corrective and Preventive Action utilizing the theory of Lean Documents - By Compliance Global Inc.

 

Category: Compliance-Regulation

Training Provider: Compliance Global

Webinar On theory of Lean Documents of applying lean principles to the creation, design, process, and management of controlled documents found in regulated industries

      
 

 Designing and Using KPIs and Performance Dashboards Webinar

 

Category: FINANCE/INVESTING

Training Provider: Online Compliance Panel

Designing, developing and supporting an effective reporting system of leading and lagging KPIs (Key Performance Indicators) is complicated. Information needed for senior management is different and less granular than that needed for the line manager, and the producers. The technical aspects of pulling the right information from the mountains of data at the right time can be overwhelming.

      
 

 Due Diligence of Quality Systems for Medical Device Companies Webinar

 

Category: Compliance-Regulation

Training Provider: Online Compliance Panel

Webinar on Due Diligence of Quality Systems for Medical Device Companies. Poor due diligence can lead to issues like recalls or warning letters.

      
 

 Expense vs Capitalize? The New Regulations Webinar

 

Category: Compliance-Regulation

Training Provider: Online Compliance Panel

Learn everything about the new IRS Tangible Property regulations. Attend this webinar if you are a Tax manager or Accounts payable professional.

      
 

 How to Perform Measurement Systems Analysis

 

Category: Compliance-Regulation

Training Provider: Online Compliance Panel

Measurement systems analysis (MSA), or gage reproducibility and repeatability (R&R), quantifies measurement variation from inspectors (reproducibility) and the gage itself (repeatability). This returns a measurement of the gage's precision, or ability to get the same result consistently from the same part. Precision is the counterpart to accuracy, or the gage's ability to get, on average, the correct measurement from a part. Gages must be precise as well as accurate to perform their jobs. While ISO 9001:2008 required only accuracy (as ensured by calibration), the automotive ISO/TS 16949 standard requires MSA as well.

      
 

 Implementing 21 CFR Part 11 - What is Computer Systems Validation and how to Implement it. - By Compliance Global Inc.

 

Category: Compliance-Regulation

Training Provider: Compliance Global

Live webinar on Computer Systems Validation Regulations and Compliance issues during System implementation

      
 

 Implementing a Change Control Quality System Successfully Webinar

 

Category: Compliance-Regulation

Training Provider: Online Compliance Panel

This web training session is designed to help attendees understand the fundamental change control steps and processes. The expert trainer will focus on change proposals, assessments, execution and final implementation of a change control quality system. The importance of proper planning, critical thinking skills, and co-ordination of all change activities will also be discussed.

      
 

 ISO 9001:2015 Key Concepts How to perform Internal Audits of Quality Management Systems based on ISO 9001 Webinar

 

Category: ENGINEERING

Training Provider: Online Compliance Panel

This course provides participants with the knowledge and skills to perform internal audits of quality management systems based on ISO 9001, or the equivalent. Participants will learn how to report on the effective implementation and maintenance of a management system in accordance with ISO 19011.The course is made for beginners in quality management and internal auditing. It provides the guidelines and requirements to develop and conduct such process and highlights the importance of ISO 9001 internal audit.

      
 

 ISO 9001:2015 Quality Management System: Preparing for a Successful Transition Webinar

 

Category: Compliance-Regulation

Training Provider: Online Compliance Panel

In this webinar our speaker Lena Cordie will train on how to carry out a gap analysis against the requirements of ISO 9001:2015 to make the transition smooth and transparent. This exercise will provide your organization with structured assistance to highlight the extent to which existing systems and controls cover the requirements of ISO 9001:2015, or to identify an implementation action plan, where needed.

      
 

 Monitoring and Validation of Pharmaceutical Water Systems

 

Category: Compliance-Regulation

Training Provider: Online Compliance Panel

This webinar will discuss the FDA requirements for design, validation and monitoring of pharmaceutical water systems. There are many different types of pharmaceutical waters and each must be fit for its intended use. Pharma water must be controlled for impurities. Pharma water systems must be designed, validated and monitored to ensure that the water produced meets specifications around the clock. Learn common pitfalls with water system design and use and how to avoid them. Get your pharma water questions answered in this webinar.

      
 

 New ISO Standard for Medical Device Quality Systems 13485: 2016 Summary of its Impact to the Medical Device Industry Professionals Webinar

 

Category: Compliance-Regulation

Training Provider: Online Compliance Panel

You will gain a thorough insight into the specific quality system requirements of all new International ISO 13485:2016 Quality System Standard requirements for Medical Devices. This timely and extremely informative webinar will truly build your knowledge from the fundamental quality principles. It will help you grow into fulfilling the quality and regulatory requirements as a professional working for medical device manufacturers of fully assembled devices and global suppliers manufacturing critical parts for the medical device industry. All noteworthy changes implemented into this key international standard will be discussed to pave the path for implementation of the changes in your organization.

      
 

 Payments and Settlements Systems - RTGS, SWIFT, LVTS, CLS

 

Category: Compliance-Regulation

Training Provider: Online Compliance Panel

This training program will focus on the entire payments and settlements process for real-time wholesale payment systems originating and receiving transactions in the US: beginning with the making of a payment and ending with the payment being received by the beneficiary and settled in a manner that makes it final and irrevocable. In it, we will explore relevant uses cases for each of these systems as well as contrast and compare their processes, risks and future trends.

      
 

 Planning and Developing Quality System Processes for a New FDA Regulated Facility Webinar

 

Category: Compliance-Regulation

Training Provider: Online Compliance Panel

Learn a practical approach to managing, developing, improving and remediating quality systems, by attending this webinar.

      
 

 Policies and Procedures Required to Support Validation of Computer Systems Regulated by FDA Webinar

 

Category: Compliance-Regulation

Training Provider: Online Compliance Panel

Learn policies and procedures required to support activities related to computer system validation for systems subject to FDA regulations in this webinar.

      
 

 Quality Systems Approach for Validation and Maintenance of a Global ERP System Webinar

 

Category: Compliance-Regulation

Training Provider: Online Compliance Panel

In the pharmaceutical industry and many other industries it is recognized that there is an increasing dependence upon automation. As a result, many companies are adopting different approaches to keeping their Enterprise systems compliant.

      
 

 System Suitability Testing for FDA and USP Compliance

 

Category: Compliance-Regulation

Training Provider: Online Compliance Panel

System suitability testing (SST) is required by USP and FDA to check and ensure on-going performance of analytical systems and methods. Both USP and EP have chapters with recommendations for system suitability tests that are enforced by FDA and other agencies. Related chapters have been updated by USP and EP and they also answer the question as to how much a method can be changed without the need for revalidation. Also, the USP chapter <1058> makes a statement that SST can substitute an instrument's performance qualification, but not further guidelines are given. This webinar will give a good understanding of FDA and USP requirements for system suitability testing.

      
 

 Understanding USP 1058 Classification for Equipment Systems in the Pharmaceutical Industry Webinar

 

Category: Compliance-Regulation

Training Provider: Online Compliance Panel

Learn about Equipment Qualification, key USP General Chapter 1058 on Analytical Instrument Qualification, history of GAMP classification, more.

      
 

 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.

      
 

 Using Metrics to Monitor and Improve Quality Management System Webinar

 

Category: Compliance-Regulation

Training Provider: Online Compliance Panel

Learn to determine what to measure, how to present information, and how to escalate issues for management review, how to prepare metrics and dashboards.

      
 

 Verifying and Validating HACCP Plans - By Compliance Global Inc.

 

Category: FOOD INDUSTRY

Training Provider: Compliance Global

live webinar on HACCP Plans for your knowledge about monitoring, verification and validation activities applied to HACCP system

      
 

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