Best-in-Class Documentation for CSV Program

Computer Systems Validation (CSV) is required by the FDA and many other international regulatory agencies. However, it is often unclear what steps to take to implement a successful Computer Systems Validation Program.

In this 1-hour free webinar, you will learn:

  • How to establish and structure an effective CSV Program?
  • Which high-quality documents need to be created and maintained for a successful CSV Program?
  • What are the required Standard Operating Procedures (SOPs) and how to create them?
  • What content should be included in which CSV document?
  • What makes CSV deliverables, SOPs, and templates “best-in-class”?
  • What auditors are looking for a successful CSV Program?

You will discover common mistakes and how you can avoid them. This webinar also provides you with a walk-through process of Computer System Validation key deliverables.

Computer System Validation Webinar Topics

  • What are the steps you need to take to implement a Computer System Validation program?
  • What is the best structure for CSV Program Documents and Tools?
  • What is Global Policy? What are the examples?
  • What is Validation Master Plan? How to create it?
  • What is an SOP? What are the SOPs required for CSV and how to create them?
  • What is Work Instruction (WI)?
  • What are the CSV templates you should develop? What content should be included?
  • Why should you have a successful CSV Program?


Cost: FREE

We are offering this webinar on the following dates: