2020 - Lifecycle Management of Analytical Methods and Procedures - according to new FDA and USP guidelines
Date2020-09-14 - 2020-09-15
Deadline2020-09-04
VenuePhiladelphia, PA, USA - United States
KeywordsEquipment calibration; System validation; 21 CFR Part 211
Topics/Call fo Papers
Managing analytical methods and procedures according to the lifecycle approach has been recommended in recent FDA guidance documents and stimuli articles published by the USP. For example, the recent FDA guidance “Analytical Procedures and Methods Validation for Drugs and Biologics” contains a section on Lifecycle Management of Analytical Procedures.
This 2-day workshop will explain the background to the new Analytical Procedure Lifecycle guidelines and give attendees the knowledge needed to implement recommended approaches. Interactive exercises will be included in the workshop.
This 2-day workshop will explain the background to the new Analytical Procedure Lifecycle guidelines and give attendees the knowledge needed to implement recommended approaches. Interactive exercises will be included in the workshop.
Other CFPs
- The Drug Development Process from Concept to Market
- The Drug Development Process from Concept to Market
- Lifecycle Management of Analytical Methods and Procedures - according to new FDA and USP guidelines
- Lifecycle Management of Analytical Methods and Procedures - according to new FDA and USP guidelines
- Lifecycle Management of Analytical Methods and Procedures - according to new FDA and USP guidelines
Last modified: 2020-04-03 23:31:53