According to current GMP guidelines, all aseptic manufacturing of sterile products should be managed by applying Quality Risk Management principles that provide a proactive means of identifying, scientifically evaluating and controlling potential risks to quality.
As 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.
Steve Marnach
During the webinar viewers 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
Speaker
Steve Marnach, Training expert Protective Apparel EMEA, DuPont Personal Protection.
The webinar will be available on Monday, 25 November, 2019 at 11 am CET (10 am UK).
Contact www.ipp.dupont.com or visit Tyvek.co.uk/isoclean for more information.
