Pfizer’s Implementation of a Rapid Sterility Method: From Bold Idea to Completed Project in Record Time
Pfizer’s goal was to create a sterile injectable and quickly release it for global deployment, all without risking patient safety. They turned to Celsis® ATP bioluminescence technology to test their product for sterility and Charles River helped them create a strategy to streamline their validation timeline. Through this partnership, Pfizer was able to expedite the system validation to a mere nine-and-a-half-months.
MicroLearning: On-Demand Microbiology Video Series
The importance of staying up to date on methods and technology is critical to ensuring a successful environmental monitoring (EM) program. Our free MicroLearning video series allows you to learn at your own pace with concise content presented by our technical experts.
Frequently Asked Questions (FAQs) for Microbiology Testing
- What regulatory standards do Charles River’s microbial testing products and services follow?
Where can I find pricing for quality control microbiology testing?
You can request a price list for our portfolio of available microbial testing products and services.
- What industries does Charles River’s microbial testing support?
What are the key market drivers for the pharmaceutical industry?
Data integrity and contamination control are among the top industry priorities for releasing safe products to the public during the COVID-19 pandemic and beyond. Our portfolio of advanced QC microbiology tools addresses these and other key market drivers while streamlining processes and addressing regulatory changes.
Why is data integrity one of the top priorities for quality control in microbiology testing?
Ensuring that data microbial testing data is accurate, relevant, and reliable is key for supporting everyday decisions. Regulatory agencies like the FDA expect organizations to be proactive in complying with data integrity laws and regulations.