The FDA’s Center for Drug Evaluation and Research (CDER) and the Center for Devices and Radiological Health (CDRH) invite you to interact with and learn directly from FDA’s regulatory experts.
Attendees will leave with a set of tools to assist in preparing regulatory filings and interacting with the FDA.
Attend virtually. Participants can join us “Virtually through Adobe Connect” [To test your computer’s connection, please visit: Adobe Connect Diagnostic Test]. Once registered, please honor your registration commitment to help us plan and deliver this conference more efficiently.
Continuing Education. This 2-day conference has been pre-approved by RAPS, SOCRA, SQA, and ACRP. Credit hour guidelines vary by organization.
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