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Read more about the article Validating Depyrogenation Process: Meeting Ph. Eur. 5.1.12 Guidelines
Validation and Qualification

Validating Depyrogenation Process: Meeting Ph. Eur. 5.1.12 Guidelines

In pharmaceutical manufacturing, particularly for parenteral preparations, equipment and primary packaging materials must be free from pyrogens.…

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August 6, 2025
Read more about the article Objectionable Microorganisms in Nonsterile Pharmaceuticals
Microbiology

Objectionable Microorganisms in Nonsterile Pharmaceuticals

The non-sterile products are subjected to two tests, microbial enumeration test and test for specified microorganisms. The…

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August 6, 2025

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