White Paper – Prevention of Contamination and Cross-Contamination in Medicinal Manufacturing Facilities

Prevention of Contamination and Cross-Contamination in Medicinal Manufacturing

This White Paper explores the methods of preventing contamination and cross-contamination in manufacturing facilities.

Purpose

  • 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.

Audience

  • Project Managers
  • Validation professionals
  • QA professionals

Prerequisites

  • 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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