The role of in vitro testing in modern cosmetic development Ensuring the safety and performance of cosmetic products is a critical requirement for manufacturers operating in today’s regulated and ...

In this chapter, we focus on two topics: the lack of enforcement of existing U.S. Department of Defense (DOD) guidelines and procedures and the role of the program manager in the acquisition process.

Cell and gene therapies require novel quality control methods due to their complex, variable nature and limited shelf life, challenging traditional pharmaceutical testing approaches. Manufacturers ...

The ambitious task on hand is apparent from the weighty title of the report – ‘Landscape Analysis on Alternatives to Animal Testing for Drug Development in India.’ That the report has the foreword by ...

WASHINGTON, D.C. — Federal regulators are moving to reduce the use of animal testing in drug development, issuing new guidance to help drugmakers adopt alternative methods that rely on human-based ...

Please provide your email address to receive an email when new articles are posted on . The FDA announced plans in 2025 to reduce animal testing requirements in biomedical research. New approach ...

EPA PFAS Regulations in 2026 -- EPA expanded PFAS monitoring, testing methods, and drinking water implementation efforts, including outreach to public water systems under the PFAS OUT Initiative. -- ...