Good Documentation Practices to Support FDA Computer System Validation and Compliance

Good Documentation Practices to Support FDA Computer System Validation and Compliance
Product Code: : FDAQ-9259
Speaker : Carolyn Troiano
Date : 28th May 2019
Time : 11:30 AM PST | 02:30 PM EST
Duration : 90Min

Overview:

Computer system validation has been regulated by FDA for more than 35 years, as it relates to systems used in the manufacturing, testing and distribution of a product in the pharmaceutical, biotechnology, medical device or other FDA-regulated industries.  The FDA requirements ensure thorough planning, implementation, integration, testing, and management of computer systems used to collect, analyze and/or report data.

In preparing all of the Computer System Validation (CSV) deliverables, it is necessary to document the work in compliance with FDA requirements.  You will learn about the best practices for ensuring your documentation meets the Agency’s standards.

Why Should You Attend:

This webinar is intended for those working in the FDA-regulated industries, including pharmaceutical, medical device, biological, animal health and tobacco.  Functions that are applicable include research and development, manufacturing, Quality Control, distribution, clinical testing and management, adverse events management and post-marketing surveillance.

You should attend this webinar if you are responsible for planning, executing or managing the implementation of any system governed by FDA regulations, or if you are maintaining or supporting such a system.

You will learn the best practices for ensuring that all of your Computer System Validation (CSV) deliverables and documentation are prepared in accordance with FDA requirements and meet compliance guidelines.

Areas Covered in the Session:

  • Learn the requirements for documenting efforts related to systems governed by FDA
  • Discuss the best practices for documenting computer system validation efforts, including requirements, design, development, testing and operational maintenance procedures
  • Review examples of incorrect, incomplete, or otherwise inappropriate and non-compliant documentation and understand why these are not acceptable
  • Learn how to prepare a procedure that will capture the best practices for FDA compliant documentation
  • Discuss the importance of training as it relates to good documentation practices to ensure FDA compliance
  • Q&A

Who will Benefit:

  • Information Technology (IT) Analysts
  • IT Developers
  • IT Support Staff
  • QC/QA Managers and Analysts
  • Clinical Data Managers and Scientists
  • Compliance Managers and Auditors
  • Lab Managers and Analysts
  • Computer System Validation Specialists
  • GMP Training Specialists
  • Business Stakeholders using Computer Systems regulated by FDA
  • Regulatory Affairs Personnel

Speaker Profile:

Carolyn Troiano has more than 35 years of experience in the tobacco, pharmaceutical, medical device, and other FDA-regulated industries. She has worked directly, or on a consulting basis, for many of the larger pharmaceutical and tobacco companies in the US and Europe, developing and executing compliance strategies and programs.


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