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