Prevention of Contamination and Cross-Contamination in Medicinal Manufacturing
This White Paper explores the methods of preventing contamination and cross-contamination in manufacturing facilities.
- To identify potential contributors of contamination and cross contamination.
- To offer ideas on how to minimise and prevent contamination and cross contamination occurring within a manufacturing facility.
- Project Managers
- Validation professionals
- QA professionals
- Familiarity with Annex 15 Qualification & Validation of the EU GMP Guide or the PIC/S GMP Guide
- General Knowledge of Qualification and Validation of facilities, utilities, systems and equipment
You can download the whitepaper “Prevention of Contamination and Cross-Contamination in Medicinal Manufacturing Facilities” here.
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