Drug Master Files (DMFs) - Understanding and Meeting Your Global Regulatory and Processing Responsibilities By compliance2go 2011
14 Sep 2011
Webinar
Drug Master Files (DMFs) - Understanding and Meeting Your Global Regulatory and Processing Responsibilities training will discuss
The relationship between DMFs and drug and biologics applications.
Who really needs a DMF and why?
The various types of DMFs - which is best for your products.
Common DMF errors - how to avoid them.
The symbiotic relationship between DMFs and current Good Manufacturing Practices (cGMPs).
Ramifications of inadequate preparation and/or maintenance and recent enforcement actions and inspectional trends.
How to deal with deficiency letters and their origins.
Effective change control strategies.
Drug Master Files (DMFs) - Understanding and Meeting Your Global Regulatory and Processing Responsibilities brings together personnel responsible for:
Regulatory Affairs
Manufacturing
Quality Assurance & Control
Research and Development
Validation
Past Events
Drug Master Files (DMFs) - Understanding and Meeting Your Global Regulatory and Processing Responsibilities By compliance2go 2011 - 14 Sep 2011, Webinar (17639)
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Important
Please, check "Drug Master Files (DMFs) - Understanding and Meeting Your Global Regulatory and Processing Responsibilities By compliance2go" official website for possible changes, before making any traveling arrangements
