Pharmaceutical Laboratory Instruments: A Beginner’s Guide Pharmaceutical Laboratory Instruments play an important role in the testing, analysis, monitoring, and quality control of medicines, raw materials, intermediates, and finished products. From…
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Pharmaceutical quality cannot depend only on testing the finished product. Quality must be controlled throughout the manufacturing process to ensure that each critical step is performed within approved requirements. In-process…
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Dissolution Testing in Pharmaceutical QC: Principle, Procedure and Acceptance Criteria Dissolution Testing in Pharmaceutical QC is an important quality-control test used to evaluate the release of an active pharmaceutical ingredient…
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Change Control in Pharmaceutical Manufacturing: 8 Essential Steps Change Control in Pharmaceutical Manufacturing is a structured quality-system process used to evaluate, approve, implement, and document proposed changes that may affect…
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Market Complaint Handling in Pharmaceutical Industry: 8 Essential Steps Market Complaint Handling in Pharmaceutical Industry is a quality-system activity used to receive, assess, investigate, document, and appropriately close complaints related…
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QA review vs QC review is an important distinction in pharmaceutical manufacturing because Quality Assurance (QA) and Quality Control (QC) perform different but complementary activities. QC primarily focuses on testing…
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Disinfectant efficacy testing in pharmaceutical industry practice helps demonstrate that a selected disinfectant can effectively reduce or eliminate microorganisms under defined conditions of use essential for maintaining microbiological control in…
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SOP lifecycle in pharmaceutical industry refers to the controlled process used to create, review, approve, issue, implement, revise, and retire Standard Operating Procedures (SOPs). SOPs are important GMP documents because…
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Revalidation in Pharma: When and Why Is It Required? Revalidation in pharma is the documented process of confirming that a previously validated process, system, equipment, or method still performs as…
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Introduction Maximum Valid Dilution (MVD) is an important concept in bacterial endotoxin testing (BET). It defines the maximum allowable dilution of a test specimen at which the endotoxin limit can…
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