Dublin, Feb. 27, 2025 (GLOBE NEWSWIRE) -- The "3hr Virtual Seminar - Validation, Verification and Transfer of Analytical Methods - Implementing Guidelines from FDA/EMA, USP and ICH" training has been ...
Dublin, April 21, 2023 (GLOBE NEWSWIRE) -- The "Analytical Method Validation, Verification and Transfer Virtual Seminar" training has been added to ResearchAndMarkets.com's offering. Dependable ...
DUBLIN--(BUSINESS WIRE)--The "Analytical Method Validation, Verification and Transfer Virtual Seminar (Oct 7th - Oct 9th, 2025)" has been added to ResearchAndMarkets.com's offering. Dependable ...
This seminar will discuss how to use modern lifecycle management and quality by design principles to ensure method robustness for easy transfer and to avoid OOS ...
When transferring a method from R&D to quality control, success hinges on discovering where “the best” and “the most reliable” intersect. Analytical method transfer suffers from many of the same ...
The attributes of the DS or DP that are to be tested to obtain the necessary information about product quality safety and efficacy are determined during the Drug Development stage. The information ...
The authors present two concepts to improve robustness and facilitate continuous improvement in analytical methods. This article contain bonus online material. This paper has been constructed to ...
Method development in the modern HPLC laboratory is challenging but can be approached very logically and is hugely rewarding when a fit for purpose method is produced. This course provides you with ...
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