No matter the age of a facility, it is imperative that biopharma manufacturing processes consistently yield high quality products that are safe for consumers. In addition to keeping a “Fit Facility”, prevention of microbial ingress within any biologics process offers numerous challenges. If any measure or control is ignored or discounted, the frequency of a contamination event can increase exponentially. Any risk to the process should be acknowledged and remediated when possible, even when considered quantitatively low.
In this webinar, CRB experts Andrew Harris, Allan Bream and Joe Povenski share their tips and tricks for developing a personalized, on-site, fit facility concept that addresses the “health” of your operation. They also highlight a bioburden control strategy case study that will help attendees understand the importance of mitigating operational risks and ensuring the upkeep of a Fit Facility.
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