Webinar "Quality Risk Management for cleanroom garment qualification in the light of GMP Annex 1" 25th NOVEMBER
According to current GMP guidelines all aseptic manufacturing of sterile products should be managed by applying QualiRisk Management principles, that provide a proactive means of identifying, scientifically evaluating and controlling potential risks to quality.
Because many factors contribute to the overall quality and suitability of cleanroom garment systems, the cleanroom garment qualification process is very important. DuPont as a company focused on protection and a cleanroom garments manufacturer prepared a free of charge webinar dedicated to all industries dealing with aseptic manufacturing.
During the webinar you will have the unique chance to learn about QRM principles for cleanroom garments, understand contamination risks as well as validation processes, all in the light of latest draft of GMP Annex 1.
Key topics of the webinar:
- Current regulatory guidance GMP Annex 1
- Understanding contamination process
- Step by step cleanroom garment qualification process