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Introduction to Biopharmaceutical Manufacturing

*Course Dates TBA

Attendees will gain an understanding of how biopharmaceuticals are made, the regulatory requirements and support systems necessary to produce safe and effective biopharmaceutical therapeutics. The course covers topics including biopharmaceutical risk management, quality control, and maintenance of standards for production. By the end of the course, participants will have a solid grasp of the fundamentals of biopharmaceutical production.

Fundamentals of Good Manufacturing Practices for Biopharmaceuticals

Thursday Mornings, April 11, 2024 – June 13, 2024

11:00 AM - 2:00 PM Eastern

Participants will gain an understanding of the regulatory requirements and industry practices necessary for the manufacturing, development, and licensing of Biopharmaceuticals, including methods and requirements. The course also covers emerging trends and risk management strategies for ensuring Biopharmaceutical quality and safety.

Implementation of Single-Use Technology in Biopharmaceutical Production

Tuesday Mornings, May 14 – July 23, 2024 (No class July 2)

11:00 AM - 2:00 PM Eastern

Participants will gain a solid understanding of current good manufacturing practice (cGMP) guidelines, SUS application, and different types of SUS. The course will explore the fundamentals of biopharmaceutical production and provide attendees with the knowledge necessary to produce human therapeutics.