Root Cause Analysis (RCA) in Pharma QA: Enhancing Pharmaceutical Quality Assurance
Master RCA in Pharma QA to identify root causes, prevent recurrences, and enhance quality. Essential for compliance and patient safety.
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Master RCA in Pharma QA to identify root causes, prevent recurrences, and enhance quality. Essential for compliance and patient safety.
Dr Binh Nguyen explains why understanding bioburden control is pivotal to a pharma manufacturer and testing laboratory
Understand the comprehensive role third-party laboratories play in enhancing accuracy, credibility, and innovation in controlled substance testing
As regulatory bodies like the FDA and USP continue to emphasize method validation and bioequivalence, laboratories must ensure their dissolution testing practices are scientifically sound and regulatory compliant.
Rigorous analytical testing ensures that APIs meet the highest standards for identity, purity, potency, and stability—safeguarding patient health and maintaining market confidence.
Tentamus' network of highly specialized laboratories aim to offer on-site safety and quality testing services in the shortest time possible
This CDMO specializes in new chemical entity (NCE) molecule, NDA 505(b)(2), and ANDA development programs
This CRO has a fully-equipped analytical laboratory and a lab-scale packaging facility
This CRO delivers FDA ready, cGMP-compliant analytical solutions quickly to keep drug development programs on track
Since 1998, this contract laboratory provides analytical and microbiological testing for the pharma industry.
They develop and perform GMP potency assays for a wide variety of drugs, proteins, monoclonal antibodies, vaccines and gene therapies
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