BOCA RATON, Fla.--(BUSINESS WIRE)--LGM Pharma, a leading provider of tailored API and CDMO services for the full drug product lifecycle, announced today the expansion of its Analytical Testing ...

Faster test results replace the standard 14-day USP sterility test SAN CARLOS, Calif., April 29, 2026 (GLOBE NEWSWIRE)-- Sapho Bio, a biotechnology company developing a rapid microbiology release ...

Currently established rapid methods for sterility testing of advanced therapy medicinal products (ATMPs) are mostly based on growth-based processes or the detection of metabolic activities. However, ...

Seoul National University College of Engineering announced that a research team led by Professor Sunghoon Kwon from the Department of Electrical and Computer Engineering, in collaboration with ...

Recipharm, a CDMO, opened its newly-commissioned parenteral development and sterility laboratories at its Bengaluru site in India. The parenteral development laboratory is designed to accelerate the ...

Nelson Labs, a Sotera Health company and leader in microbiological testing, has expanded its rapid microbiological methods (RMMs) for product-sterility testing at three laboratory sites in the U.S.

Robust sterility testing is essential to ensure the safety of cell therapies. However, traditional culture-based analysis takes several weeks to confirm a therapeutic’s microbial contamination, which ...

ACROBiosystem's SAFENSURE ™ Sterility Rapid Detection Kit is a validated NAT-based sterility rapid detection kit designed to accelerate in-process and lot-release testing. The Sterility Rapid ...

Nelson Labs, a Sotera Health company and a specialist in microbiological and analytical chemistry testing and advisory services for the medical device and pharmaceutical industries, now performs ...

To evaluate the sterility, stability, and efficacy of repackaged ziv-aflibercept in 1-mL plastic tuberculin syringes for intravitreal injection after storage for up to 90 days at controlled (4 °C) and ...

This interview addresses the challenges and complexities of developing and manufacturing controlled-release drug formulations. Could you introduce yourself and your expertise in drug development and ...