Vendor Management for Pharmaceuticals, Biologicals, and Medical Devices

This webinar provides an overview of FDA’s requirements for vendor management and oversight for pharmaceuticals, biologicals, and medical devices.

Why Should You Attend:

FDA requires pharmaceutical, biological, and medical devices manufacturers to establish and maintain control over their suppliers to ensure the purchased goods or services meet Good Manufacturing Practices.

In this webinar, you will learn FDA’s expectations for the implementation and on-going operation of an effective vendor oversight program.

Areas Covered in the Webinar:

• Pharmaceuticals
• Biologicals
• Medical devices
• Finished Product (contract manufacturing)
• Chemicals (including Active Pharmaceutical Ingredients and excipients)
• Packaging Materials (primary, secondary, & tertiary)
• Labelling (printed) Materials
• Services (including contract laboratories and contract sterilizers)

Who Will Benefit:

Pharmaceutical, biological, and medical device company personnel working in production, R&D, regulatory affairs, QA, and QC.