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 ...

For a drug-development process that relies on outsourced services, special considerations are needed to ensure the proper transfer of technology and information from one phase to the next. Hayes: The ...

Antibody-drug conjugates (ADCs) and other next-generation drug modalities are unlocking new treatment possibilities. However, ...

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 ...

This vendor-neutral ISR guide is designed to educate pharmaceutical scientists on using the technique to effectively assess the quality of bioanalytical methods. It contains up-to-date information on ...

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 ...

DUBLIN--(BUSINESS WIRE)--Research and Markets has announced the addition of the "Pharmaceutical Analytical Testing Outsourcing Market Analysis By Services (Bioanalytical Testing, Method Development ...

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 ...

NEW YORK, Feb. 28, 2017 /PRNewswire/ -- The global pharmaceutical analytical testing outsourcing market is expected to reach USD 9.6 billion by 2025, according to a new report by Grand View Research, ...