Free Live Webinar 'Endotoxin and sterility testing for sterile pharmaceutical products'
Ensuring sterilization and microbiological safety of the pharmaceutical products is an essential part of the drug quality control process regulated by the USP, EP, and JP Pharmacopeias. Compendial sterility and endotoxin tests are used as finished product quality control release tests and are required to demonstrate that the product batch is safe for human usage.
During this webinar our experts will get you familiarized with endotoxin and sterility testing and discuss the common challenges related to creating a suitable product-specific test method to achieve reliable test results
Following topics are going to be covered:
- Endotoxin Testing (LAL test) background, its importance and test principles
- Common sterility testing procedures
- Importance of suitability testing in both endotoxin and sterility testing
At the end of the webinar there is going to be a live Q&A Session, where Eurofins experts are going to discuss the most important aspects in more detail.
Who should attend:
BioPharmaceutical scientists, managers, quality and regulatory control specialists
About the speakers:
Tanja Wiersch, Study Director Microbiology, Eurofins BioPharma Product Testing
Teresa Friedrich, Group Leader Sterile & Non-sterile products, Eurofins BioPharma Product Testing
The webinar is now available on-demand
Webinar language: ENGLISH
