With regulations only becoming more stringent and new biologics being discovered regularly, performing bioburden, sterility and microbial limit testing of raw materials, intermediates or finished products is a crucial step in the dynamic work done by pharmaceutical producers every day.
Cross-contamination during testing can result in false positives requiring costly retests and delaying your products from reaching the market.
This webinar will cover topics to help labs prevent contamination while also saving money.
In this webinar you will learn:
Global Product Manager
Microbiology QC Portfolio
Lab SLS Manager – North America
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