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

30 Mar 2012

Webinar

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

Past Events

Quality Agreements with Pharmaceutical/ Biologic Manufacturers and the Use of Drug Master Files: Understanding and Meeting your Regulatory and Processing Responsibilities 2012 - 30 Mar 2012, Webinar (22219)

Quality Agreements with Pharmaceutical/ Biologic Manufacturers and the Use of Drug Master Files: Understanding and Meeting your Regulatory and Processing Responsibilities 2026

Important

Please, check "Quality Agreements with Pharmaceutical/ Biologic Manufacturers and the Use of Drug Master Files: Understanding and Meeting your Regulatory and Processing Responsibilities" official website for possible changes, before making any traveling arrangements

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Health & Medicine: Pharma

Industry: Food & Beverages

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