Description
Laboratories that work in a GMP environment are required to have documentation to show they are qualified to run specific, consistent and reliable analytical test methods. Method qualification of a method can be achieved in three ways: Validation, Verification (Compendial Methods) and Method Transfer (company methods). Lack of such documentation can result in warning letters from both the FDA and Health Canada. This webinar discusses how to execute meaningful Method Transfers of company methods by selecting appropriate analytical performance characteristics and acceptance criteria, documentation of the transfer process and how to avoid failures.
Why should you attend: Have you ever wondered why method transfer of analytical methods is necessary? Do you experience failures with Method Transfers? Are you interested in how to prevent these failures? If you answered yes to any of the above questions or would simply like confirmation of your current approach to analytical method transfer, then this webinar is for you.
