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Read more about the article Pharmaceutical Equipment Qualification: From URS to Routine Usage
Equipment / Validation and Qualification

Pharmaceutical Equipment Qualification: From URS to Routine Usage

The pharmaceutical equipment qualification process requires precision, quality, and adherence to regulatory compliance. Any deviation in equipment…

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August 8, 2025
Read more about the article Risk Assessment for Environmental Monitoring in Sterile Injectable Facilities
Environmental Monitoring

Risk Assessment for Environmental Monitoring in Sterile Injectable Facilities

Among the many elements of Good Manufacturing Practices (GMP), a robust environmental monitoring (EM) program plays an…

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August 8, 2025

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