Best-in-Class Documentation for CSV Program – December 2024
December 17 @ 11:00 am - 12:30 pm CST
Free Webinar
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
