| Greetings!
We are excited to invite you to a free online workshop designed to provide an introduction to Computer System Validation (CSV) in regulated industries such as pharmaceuticals, medical devices, and logistics. This brief, high-level session will cover the core principles of CSV, key regulatory requirements, and the basics of the validation process, including GAMP®5 and 21 CFR Part 11 compliance. By attending, you will gain valuable insights into why CSV is essential for ensuring the integrity and compliance of computerized systems in regulated environments.
This workshop is ideal for professionals new to CSV or those seeking a quick overview of its significance in regulated industries. It will be particularly beneficial for individuals working in quality assurance, compliance, IT, and regulatory affairs roles within pharmaceutical, medical device, and logistics companies.
During the session, we will explore the basics of CSV, key regulatory frameworks such as GAMP®5 and 21 CFR Part 11, and introduce the System Development Life Cycle (SDLC) in the context of validation. By the end of the workshop, participants will have a clearer understanding of CSV’s importance, regulatory requirements, and the validation process.
We encourage you to reserve your spot soon to ensure your participation in this informative session.
Looking forward to your attendance! | 
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