The United States Pharmacopeia emphasizes mechanical calibration and a performance test to esnure integrity of the dissolution procedure. In October 2007, the USFood and Drug Administration released a ...
USP applies metrological principles to the dissolution procedure alone and in collaborative studies to understand and minimize potential sources of variability. According to the International ...
Dissolution and drug release tests are directly relevant to the safety and efficacy of many common pharmaceutical dosage forms. To achieve reliable and reproducible results, analysts must understand ...
DUBLIN, Feb. 26, 2020 /PRNewswire/ -- The "Pharmaceutical Dissolution Testing" conference has been added to ResearchAndMarkets.com's offering. This three-day course covers the theory behind drug ...
System addresses the pharmaceutical industry’s need for compliant, semi-automated testing of nanoparticle drug formulations. SANTA CLARA, Calif.--(BUSINESS WIRE)-- Agilent Technologies Inc. (NYSE: A) ...
The Media-Mate Plus is the perfect media-prep system for a busy dissolution lab that demands both speed and accuracy. It delivers pre-heated, filtered, deaerated, and volumetrically dispensed media to ...
In addition to use of dissolution testers, this three-day course will also cover equipment qualification, development and validation of dissolution procedures, and the use of dissolution testing in ...
SANTA CLARA, Calif.--(BUSINESS WIRE)--Agilent Technologies Inc. (NYSE: A) today announced the introduction of the NanoDis System for nanoparticle dissolution testing. Combining Agilent instrumentation ...
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