Jan 11, 2018 - Jan 12, 2018 | 9:00 AM - 6:00 PM Add to Calendar 11-01-2018 09:00 12-01-2018 18:00 America/Toronto What is Process Validation Report | 21CFR11 Compliance Checklist 2018 Course ...

Developing a medical device is a lengthy process. Prior to commercial distribution, FDA requires that the manufacturing process for the product be validated. Process validation is defined as the ...

The authors outline a validation approach for the manufacture of a “legacy product,” taking into consideration recent guidelines. The aim is to demonstrate the validity and capacity of the ...

The renewal of European regulations regarding pharmaceutical process validation in autumn 2001 has been the subject of much discussion. The purpose of this article is to summarize and review the ...