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
KeywordsUSP <1058>; EU Annex 11; Use of Excel in QC Laboratory
Topics/Call fo Papers
Results of analytical methods are used as the basis for important decisions during development and manufacturing of pharmaceutical products. All regulatory agencies expect the regulated industry to have procedures in place to ensure suitable levels of reliability, accuracy and precision of such methods. The procedures should cover lifecycle phases from design, development, validation to on-going routine use.
Other CFPs
- Analytical Instrument Qualification and System Validation
- Laboratory Inspection and Auditing
- Validation, Verification and Transfer of Analytical Methods (Understanding and implementing guidelines from FDA/EMA, USP and ICH)
- SWS Florence ART 2020 - The Magic of Renaissance
- Validation, Verification and Transfer of Analytical Methods (Understanding and implementing guidelines from FDA/EMA, USP and ICH)
Last modified: 2020-04-04 00:23:43