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The Office of Pharmaceutical Quality (OPQ) in the US Food and Drug Administration (FDA)’s Center Pharmaceutical Quality for Drug Evaluation and Research (CDER) has released its 2022 annual report analysing drug manufacturers and their products. FDA’s sampling and testing programme found 892 of 1,552 productsamples (57.5
Responsible for Media Fill, Cleaning Validation, Finished ProductSampling. Process Validation, Bulk Sampling, Line Clearance, Production Line Monitoring. QA BPCR REVIEW : •Issuance and checking of BPCR’s as per the batch requisitions initiated by Production.
But despite this surge in demand, research from GlobalData shows that many CMOs have decreased in-house, non-containment, small molecule manufacturing. These turnkey solutions cover every process through the drug manufacturing life cycle. Finding the right solution.
Although sales managers strive to ensure every member of their team has access to introductory videos, pamphlets, productsamples, and data from recent studies, most still rely on the same methods of measuring field force effectiveness the industry has relied on for decades. That’s a lot of information.
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