Webinar - Online
A description of the various stages and sections of a Master Regulatory File (MRF) System. As an investigational product progresses through development key studies, decisions, regulatory communications, manufacturing progression are accumulated and necessary to reference as the NDA and MAA applications are made.Therefore MRF systems needs to preplanned and have sections to organize this information. Although this won’t be discussed this organization is applicable to a well managed document management system.
Organization: Global Compliance Trainings
For more information, please visit: http://www.globalcompliancetrainings.com/index.php?rout...
May 25, 2014 (10:00 AM - 01:00 PM)
201,N Squirrel road, Suite 1007, Auburn Hills, Michigan United States - 48326
Contact: John Gordan (webinar@globalcompliancetrainings.com)
Phone: 2482120588
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