#23: A Device Primer: 510(k)s, PMAs, IDEs
Jun 23 2013 8:30AM - Jun 23 2013 12:00PM | Boston Convention and Exhibition Center
415 Summer Street,
Boston, MA 02210
Who Should Attend
This tutorial is designed for regulatory affairs (RA) managers, business development managers and staff; principal investigators, IRB members, clinical research associates (CRAs), academic sites; lawyers, R&D, and those working on combination products, cross-functional medical products and those wishing an introduction to devices.
Unless otherwise disclosed, the statements made by speakers represent their own opinions and not necessarily those of the organization they represent, or that of the Drug Information Association. Speakers, agenda and CE information are subject to change without notice. Recording of any DIA educational material in any type of media is prohibited without prior written consent from DIA.
Participants with Disabilities:
Reasonable accommodations will be made available to persons with disabilities who attend an educational activity. Contact the DIA office in writing at least 15 days prior to event to indicate your needs.