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(Registration is required)
We are pleased to announce the Spring 2016 Regulatory Education for Industry (REdI) Conference, an FDA-led forum that brings together the regulatory educators from FDA’s Center for Drug Evaluation (CDER) and Center for Devices and Radiological Health (CDRH). The goal of this conference is to provide direct, relevant, and helpful information on the key aspects of drug and device regulations. Our primary audience is that of small manufacturers of drug and/or device medical products who want to learn about how FDA approaches the regulation of drugs and devices.
Featuring a Drug-Device Plenary Session on
FDA Insights on Products for Rare Diseases and Pediatrics
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This 2-day conference has been pre-approved by RAPS as eligible for up to 12 credits towards a participant's RAC recertification upon full completion.
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HOTEL ROOM BLOCK CUT OFF DATE IS APRIL 25, 2016.
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We ask that you honor your registration commitment.
If you are registered and are unable to attend please contact events@nakamotogroup.com
For conference registration questions or logistical questions, contact: Nick Cane atevents@nakamotogroup.com
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