The authors demonstrate that anecdotal reports of prednisone tablet variability are inaccurate. The United States Pharmacopeial Convention provides reference standard tablets for use in performance ...
The United States Pharmacopeia emphasizes mechanical calibration and a performance test to esnure integrity of the dissolution procedure. The intent of the USP performance verification test (PVT), ...
Pharmaceutical testing is a must to ensure that all medications meet the top quality, safety, and performance requirements before they enter the market. CD Formulation’s cGMP-compliant laboratory is ...
To achieve reliable and reproducible results, it is important that analysts understand the importance of correctly setting up and sampling from the chosen apparatus. In addition to use of dissolution ...
TRADE NEWS: Agilent Technologies Introduces Dissolution Apparatus for Pharmaceutical Quality Control
SANTA CLARA, Calif.--(BUSINESS WIRE)-- Agilent Technologies Inc. (NYSE:A) today introduced the 708-DS Dissolution Apparatus, a quality control instrument that can be configured for manual and ...
Pion Inc., a leading provider of innovative analytical solutions for drug development, today announced the launch of its latest product, DissoSpec™ QC Dissolution Monitoring System, a groundbreaking ...
Teva is voluntarily recalling a single lot of Anagrelide Capsules, USP 0.5mg, due to dissolution failure that was detected during a routine stability test. Teva is voluntarily recalling a single lot ...
The All India Pharmaceutical Associations Consortium (AIPAC), in association with Small & Medium Pharmaceutical Industry Centre (SMPIC), NIPER Mohali – SAS Nagar, Punjab, Society for Pharmaceutical ...
To achieve reliable and reproducible results, it is important that analysts understand the importance of correctly setting up and sampling from the chosen apparatus. In addition to use of dissolution ...
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