Contract development and manufacturing organizations (CDMOs) occupy a unique position in the pharmaceutical industry. They have the great opportunity of being able to participate in a breadth of products, which is not generally possible in a single company. On the other hand, the logistics of working with multiple clients and various approaches can be a challenge. Success in transferring a drug product process requires multi-variant thinking. The product may still be in early clinical trials or it may be a commercial product being introduced to new markets. This webinar will consider a product, wherever it is in its lifecycle, and how consistency, planning and communication form the building blocks for success in the manufacturing process transfer.

Featured Speaker

Jo Anne Jacobs

Fellow, Manufacturing Technology Specialist

Jo Anne Jacobs is a Fellow in the Drug Product Manufacturing Science and Technology group at Catalent Biologics’ Bloomington, IN site ensuring successful technical transfers of both clinical and commercial products. She has been in the pharmaceutical industry for over twenty years, having worked in academic and commercial settings, and has extensive experience in the manufacturing of parenteral products.


Register now for this webinar