The safety and quality control of parenteral pharmaceuticals, biologics, and medical devices depend heavily on the Bacterial Endotoxin Test (BET). Historically, Limulus Amebocyte Lysate (LAL), derived ...
The safety and sterility of injectable pharmaceuticals, vaccines, and implantable medical devices depend fundamentally on the detection of bacterial endotoxins. Even in picogram quantities, these ...
Producing cGMP biopharmaceutical products requires controlled, consistent performance of the manufacturing process. cGMP also requires controlled, consistent performance of analytical test methods.
Advancing microbiology QC in biomanufacturing requires new technologies, strong cross-functional practices, and collaboration ...
PHOENIX--(BUSINESS WIRE)--Spirit Electronics, a value-added microelectronics distributor, today announced the achievement of DLA Commercial Lab Suitability for MIL-STD-883. Spirit’s qualified test ...
The latest version of Instron’s Autoinjector Testing System was developed in close collaboration with CDMOs and pharmaceutical device manufacturers. It can perform thorough functioning testing on ...
A Standard Test Method is a conclusive procedure that yields a test result. So as to achieve accurate and relevant test results, a standard test method is definite, unambiguous, and experimentally ...
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