As drug development becomes more complex, so do the demands for accurate, reproducible bioanalytical data to prove their ...

Bioanalytical method development and validation are at the forefront of ensuring rigorous, reproducible and reliable data in both drug development and clinical diagnostics. The field encompasses the ...

FDA updates guidance to reflect advances in technology. FDA has updated a 2001 guidance on bioanalytical method validation because of advances in bioanalytical technology and science. Guidance for ...

Dublin, Jan. 18, 2024 (GLOBE NEWSWIRE) -- The "Analytical Methods Validation for FDA Compliance Drugs and Biologics" training has been added to ResearchAndMarkets.com's offering. This Analytical ...

FDA is collecting public comments on a draft guidance for bioanalytical method validation developed by ICH. FDA announced the availability of a draft guidance for industry, “M10 Bioanalytical Method ...

ALEXANDRIA, Va. - The American Association of Pharmaceutical Scientists (AAPS) will present the AAPS Workshop on Bioanalytical Methods Validation – A Revisit with a Decade of Progress on January 12-14 ...

The data generated using analytical methods is essential for many of the critical decisions made in the pharmaceutical industry. To be confident in the reliability of this data it is crucial that the ...

Announcing a new article publication for BIO Integration journal. Ellagic acid (EA) is a natural polyphenolic compound recognized for bioactive and pharmacologic properties that is found abundantly in ...

Market opportunities exist in the development and validation of liquid chromatography methods and instruments for pharmaceuticals, emphasizing compliance with stringent US EPA and FDA standards to ...

The data generated using analytical methods is essential for many of the critical decisions made in the pharmaceutical industry. To be confident in the reliability of this data it is crucial that the ...