Drug Master Files (DMFs) - Understanding and Meeting Your Global Regulatory and Processing Responsibilities By compliance2go 2011

  • 14 Sep 2011
  • Webinar

Description



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

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

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Business: Innovations, Management, Marketing & Sales, Office supplies, Quality assurance
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Government & Global Issues: Law & Regulations
Health & Medicine: Healthcare, Medical device, Medical laboratories, Medical technology, Pharma
Science: Biochemistry, Chemistry, Health sciences, Life Sciences & Biology
Services: Retail

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