Webinar: Overview of Regulatory Affairs and Transition to RA Field
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Webinar: Overview of Regulatory Affairs and Transition to RA Field

Webinar: Overview of Regulatory Affairs and Transition to RA Field

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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.

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