Pharmaceutical product sterility assurance: Making it easier to release product
The quality and accreditation of culture media have a direct impact on the results and overall costs involved in operating a pharmaceutical microbiological quality control (QC) laboratory. In this webinar, learn how you can accelerate product release-to-market time, lower overhead costs and secure organizational revenue goals while meeting USP/EP/JP regulations with Thermo Fisher Scientific microbiology testing products.
Take a closer look at how these products are improving laboratory workflows while meeting important regulations.
By the end of the session, you will understand:
- Key considerations for selecting culture media products based on USP/EP/JP regulations
- How to apply the selection criteria to achieve revenue goals
- How to partner with Thermo Fisher Scientific for culture media sterility and validation needs
Who should attend?
- Pharmaceutical manufacturing professionals managing microbiology laboratories