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Supporting seamless simulations
Media fills play a crucial role in validating aseptic processing procedures and assessing potential contamination risk. At the core of effective media fills is the quality of the culture media used. Our commitment is to provide you with high quality media to ensure the reliability and integrity of your media fills.
Explore our range of pharmacopoeia harmonized cold filterable media available in both dehydrated culture media and bioprocess container formats to suit your needs, as well as our triple wrap contact and settling plates for environmental monitoring. And, complete your workflow with our ISO 17034-certified quality control microorganisms for growth promotion testing.
By simulating aseptic manufacturing processes, media fills help detect and mitigate potential contamination risks, safeguarding the quality of pharmaceutical products. Learn more about key considerations in developing a robust media fill program.
In this webinar, our expert speaker will discuss aseptic process simulations (APS), a critical component of sterility assurance. Topics include modern APS design principles, how to align simulations with actual production risks, selecting the right culture media for your APS and growth promotion testing.
In part II of our APS webinar series, our expert speaker examines how to evaluate, interpret, and integrate APS results to provide meaningful evidence of process capability, strengthen sterility assurance, and reinforce your site’s overall Contamination Control Strategy (CCS).
Featured speaker: Vanessa Vasadi Figueroa, Chief Executive Microbiologist and Independent Consultant at VVF Science®, brings over 20 years of experience in the life sciences industry, supporting Pharmaceutical, Biotechnology, and Medical Device companies.
For Laboratory Use Only. Not for use in diagnostic procedures.