Carl Patterson is a seasoned Pharmaceutical Manufacturing, Aseptic Processing, and Quality Assurance professional who is based in San Diego, California. As soon as he discovered the importance of biotechnology in the area, he was inspired to enter the pharmaceutical manufacturing industry. However Read more
This webinar on biopharmaceutical raw material testing will discuss how to implement processes for the control of microbial contamination, establish microbial limits and mitigate the risk of contamination.
Course Objectives:
Raw materials are often the major source of microbial contamination that is introduced into the manufacturing process. Raw materials of natural origin, such as animal and plant source, support an extensive and varied
This webinar will address the regulatory and industry viewpoints on
The presenter will provide specific examples, from his experience, during the course to help you better understand and control microbial contamination in raw materials arriving at your facility.
Course Outline:
• What is a biopharmaceutical Raw Material?
• Risks associated with raw materials
• What are the contaminants?
• Do you know where your raw materials come from?
• Manufacturing Processes and control of microbial contamination
• Establishing microbial limits for your raw materials
• Consequences of microbial contamination
• Mitigating the risk
What You Get:
• Training Materials
• Live Q&A Session with our Expert
• Participation Certificate
• Access to Signup Community (Optional)
• Reward Points
Who Will Benefit:
• Quality Assurance
• Quality Control
• Production
• Logistics
• Manufacturing
• Quality system auditors
• QA directors and managers
• Microbiology analysts and technicians
• Consultants
• Regulatory and Compliance Management
Training for New Technical Writers
LIVE : Scheduled on
13-January-2025 :01:00 PM EST
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