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.
Using Regulatory Master Files for Investigational Products
9 April 2014, michigan, United States
Introduction
Venue
online
online, 201,N Squirrel road,, Auburn Hills, Suite 1007, michigan, 48326, United States
Useful links
Organised by
Global Compliance Trainings
Contact information
Mr john gordan
201,N Squirrel road, Suite 1007, Auburn Hills, michigan, 48326, United States of America
2482120588
Contact us by email
201,N Squirrel road, Suite 1007, Auburn Hills, michigan, 48326, United States of America
2482120588
Contact us by email
Related events
Chemistry Teaching in Practice
9 January 2025 09:30-16:00, Oxford, United Kingdom
TAC 2025 - 60th Anniversary Conference
14 April 2025 09:00 - 16 April 2025 17:00, Guildford, United Kingdom
Top of the Bench Lancashire Local Section Heat
16 January 2025 10:00-15:30, Preston, United Kingdom
Redefining the Chemical Status Quo: Women Catalysts for Equality
11 February 2025 10:00-13:00, Abuja, Nigeria
Search
Advertisement
Spotlight
Explore
Membership
