DIA Launches Regulator Affairs Certificate Program
January 5, 2010 | DIA has announced a regulatory affairs certificate program to provide comprehensive training on current regulations and their practical application to the development and commercialization of pharmaceutical, biotechnology, medical device, and related health care products. The curriculum features courses in US Regulatory Affairs: IND and NDA/CTD Phases, EU Regulatory Requirements, Preparing for FDA Meetings, Post-approval Regulatory Requirements, Regulatory Requirements for Product Labeling and Advertising, Regulation of Drug, Medical Device, and Biologic Products, and Quality Assurance. DIA
Click here to log in.
Text Only 2000 character limit
Page 1 of 1