Trial Master File (TMF): FDA Expectations from Sponsors and Sites
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Website http://bit.ly/1Nmd3GJ |
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Category Clinical Research;
Deadline: October 14, 2015 | Date: October 14, 2015
Venue/Country: Palo Alto, U.S.A
Updated: 2015-10-07 18:45:33 (GMT+9)
Call For Papers - CFP
This training will review the essential elements of a TMF for clinical trials. The activities of set-up, maintenance, and monitoring will be discussed using case studies to highlight common deficiencies and potential solutions.Why Should You Attend:If you are involved in a clinical trial, either as a clinical site or a sponsor, this webinar will provide valuable suggestions about which documents are essential and which ones are not needed for an FDA audit. Who Will Benefit:This webinar will provide valuable information to people investing in FDA-regulated product development projects and also the following personnel:Clinical Research Associates (CRAs)Clinical Research Coordinators (CRCs)Clinical Research AdministratorsPrincipal InvestigatorsProject ManagersInstructor Profile:Dr. Mukesh Kumar is a Washington DC-based consultant in regulatory affairs and quality assurance for manufacturers and developers of FDA-regulated products. Note:Use coupon code NB5SQH8N and get 10% off on registration, Valid till Dec 31st 2015.For Registration:http://www.complianceonline.com/trial-master-file-tmf-fda-expectations-webinar-training-703078-prdw?channel=ourglocal
Keywords: Accepted papers list. Acceptance Rate. EI Compendex. Engineering Index. ISTP index. ISI index. Impact Factor.
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