This course provides an understanding of the significance of endotoxin testing in ensuring product safety and compliance with regulatory standards. This webinar highlights the importance of accurate endotoxin detection in pharmaceutical products, particularly those administered parenterally as per USP-NF General Chapters which include the following:
– <85> Bacterial Endotoxins Tests

Subject area:
Drug Products & APIs

Objectives (If applicable):
– Explain the role of USP in microbiology and sterility assurance.
– Explain the difference between pyrogens and bacterial endotoxins.
– Identify Bacterial Endotoxin Test Methods-Theory.

Target Audience (If applicable):
– QA/QC staff
– Regulatory affairs managers
– Scientists
– Microbiologists
– Investigators
– Other professionals who work or interact in a microbiology laboratory environment in Pharmaceutical, Biotech, Excipients or Allied Industries.