Webinar: Overview of Regulatory Affairs and Transition to RA Field
Regulatory Affairs (RA) professionals are essential to all aspects of the product development processes – research, pre-clinical and clinical development, market authorization and post-market surveillance of drugs, medical devices, and biotechnology products.
In this webinar we will:
1.provide an overview of the diversity of the scope, strategic importance, and the professional growth opportunity of RA;
2.explain the RA roles and responsibilities, the diverse RA functional groups, and how the RA team interacts with other functions;
3.share the experience of how RA professionals began their careers to help the people who are interested in transitioning into the RA field.