Quality Agreements with Pharmaceutical/ Biologic Manufacturers and the Use of Drug Master Files: Understanding and Meeting your Regulatory and Processing Responsibilities 2012

Quality Agreements with Pharmaceutical/ Biologic Manufacturers and the Use of Drug Master Files: Understanding and Meeting your Regulatory and Processing Responsibilitie is a webinar dedicated to advantages for drug product manufacturers and suppliers in developing these arrangements together.

Quality Agreements with Pharmaceutical/ Biologic Manufacturers and the Use of Drug Master Files: Understanding and Meeting your Regulatory and Processing Responsibilitie brings together:

• Regulatory Affairs
• Manufacturing
• Global Supply Chain
• Project Managers
• Quality Assurance & Control
• Research and Development
• Development and Preparation of Submission Materials
• Validation
• General Management