Trial Master File (TMF): FDA Expectations from Sponsors and Sites

Website http://bit.ly/1Nmd3GJ | Edit Freely

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

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 Administrators

Principal Investigators

Project Managers

Instructor 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