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PHARMACEUTICALS 2011 - Drug Master Files (DMFs) - Understanding and Meeting Your Global Regulatory and Processing Responsibilities - Pharmaceuticals webinar By ComplianceOnline
Website http://complianceonline.com/ecommerce/control/trainingFocus/~product_id=701367?channel=ourglocal |
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Category Pharmaceuticals,conference,event,Webinar
Deadline: January 12, 2011 | Date: January 12, 2011
Venue/Country: Palo Alto, U.S.A
Updated: 2010-12-03 19:57:47 (GMT+9)
Call For Papers - CFP
This DMFs (Drug Master Files) training will discuss the current review and enforcement climate within FDA and the manner in which drug master files (DMFs) are reviewed by FDA personnel. Besides the US, the use of DMFs in the EU, Canada and Australia will also be discussed. Similarities and differences to the U.S. system will be highlighted.The course offers methodologies and techniques on:Who really needs a DMF and why?The various types of DMFs - which is best for your products.The relationship between DMFs and drug and biologics applications.The symbiotic relationship between DMFs and current Good Manufacturing Practices (cGMPs).Common DMF errors - how to avoid them.How to deal with deficiency letters and their origins.Effective change control strategies.Ramifications of inadequate preparation and/or maintenance and recent enforcement actions and inspectional trends.Keywords: Accepted papers list. Acceptance Rate. EI Compendex. Engineering Index. ISTP index. ISI index. Impact Factor.
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