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Quality Assurance
Contamination and Cross-Contamination in Pharmaceutical Manufacturing
Preventing contamination and cross-contamination is of utmost importance in pha…
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Quality Assurance
Importance of Electronic Records and Signatures in the Pharmaceuticals Industry
Introduction In the digital revolution of healthcare, pharmaceutical companies …
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Quality Assurance
Common cGMP Violations in the Pharmaceutical Industry
Introduction Good Manufacturing Practices (GMP), also known as current good man…
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Quality Control
Relation between Assay and Dissolution Testing
Assay and dissolution testing are both important analytical techniques used in …
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Quality Control
SOP for Forced Degradation Study
OBJECTIVE To provide the procedure for the Forced Degradation Study SCOPE This …
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Production
SOP for Entry, Exit and Gowning procedure for Powder Processing Area
PURPOSE To define Procedure for Entry, Exit and Gowning procedure for Powder Pr…
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Pharmacopeia
USP 2023 (USP 46 –NF 41)
The United States Pharmacopeia (USP) and the National Formulary (NF) are combin…
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