Join Our Webinar Series to Ensure Compliance and Safeguard Your Biotech or Pharma Products
Monthly Series – please register for the session(s) that you would like to attend.
Microbiological contamination is a constant challenge for pharmaceutical companies even at this day and age despite the availability of programs to keep it under control. One reason for this is because the contamination itself may arise from various sources – Raw materials, lack of effective cleaning or in-process controls, humans, container closure system or sterilization failures etc. Without proper checks and controls in place, companies risk product recalls and serious adverse patient outcomes. During 2018 – 2022, more than 35 products were recalled by the U.S Food and Drug Administration (FDA) due to microbial contamination. The true number of drug products manufactured and rejected prior to distribution is expected to be much larger.
This webinar series by Sartorius will discuss the need for developing and deploying microbial test methods based on risk assessments, as well as the effective investigation of microbial contamination of drug products.
Presentations:
Understand the Types and Amounts of Microorganisms in your Drug Product with In-Process Bioburden Monitoring [POSTPONED]
21-Sep, 2023 (1.30pmSGT | 3.30pm AEST | 11.00am IST)[Special Episode] Pharma Compliant Weighing
5-Oct, 2023 (1.30pmSGT | 3.30pm AEST | 11.00am IST)Ensure Microbiologically Safe Products Using the Compendial Sterility Test Method
19-Oct, 2023 (1.30pmSGT | 3.30pm AEST | 11.00am IST)Manufacturing Short Shelf-Life Drug Products? Overcome Limitations of Lengthy Traditional Sterility Testing Methods with Rapid Testing
16-Nov, 2023 (1.30pmSGT | 3.30pm AEST | 11.00am IST)Meet the EU GMP Annex 1 Requirements with Continuous Microbial Air Monitoring of your Pharmaceutical Production Environment
7-Dec, 2023 (1.30pmSGT | 3.30pm AEST | 11.00am IST)