Blog Archive

January 17, 2025

How To Develop A Validation Master Plan

Introduction to Validation Master Plans In pharmaceutical manufacturing facilities, a validation master plan or VMP is a document companies use to ensure that they consistently create products that…
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January 08, 2025

Mastering Equipment Qualification in the Pharmaceutical Industry

Introduction to Equipment Qualification in the Pharmaceutical Industry Why is equipment qualification critical in the pharmaceutical industry? Your employees and customers depend on your…
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January 06, 2025

The Critical Role of CQV in Pharma Quality and Compliance

Introduction to CQV in Pharma What is CQV in pharma? Pharmaceutical companies implement commissioning, qualification, and validation (CQV) services to ensure product quality and patient safety. Be…
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