Drug Master Files: Understanding and Meeting your Regulatory and Processing Responsibilities 2018
16 Apr 2018
Webinar
Description
Topics
The relationship between DMFs and cGMPs
The essential components of all DMFs, including:
Tactics for dealing with unique or novel situations/unfavorable reviews
Tactics for avoiding the most common DMF-related errors
Who should Attend
Regulatory Affairs
Manufacturing
Global Supply Chain
Project Managers
Quality Assurance & Control
Research and Development
Past Events
Drug Master Files: Understanding and Meeting your Regulatory and Processing Responsibilities 2018 - 16 Apr 2018, Webinar (74595)
Important
Please, check "Drug Master Files: Understanding and Meeting your Regulatory and Processing Responsibilities" official website for possible changes, before making any traveling arrangements
Event Categories
Business: Quality assurance
Health & Medicine: Healthcare, Medical laboratories, Medical technology
