Register Now for the REdI 2020 Conference August 25-28

Dear Medical Device and Drug Innovator: The Food and Drug Administration's (FDA) Center for Drug Evaluation and Research Small Business and Industry Assistance (CDER SBIA), and Center for Devices and Radiological Health (CDRH) Division of Industry and Consumer Education (DICE) are pleased to invite you to the 2020 Regulatory Education for Industry (REdI) Annual Conference. When: August 25-26: CDER Drugs track             August 27-28: CDRH Devices track

REGISTER HERE Registration is FREE! The program themes feature the following: CDER: Post Approval Considerations CDRH: Benefit-risk principles to the total product life cycle of medical devices Attend virtually. Participants can join us “Virtually via Adobe Connect” [To test your PC, 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. For more information, please visit the REdI Conference web page. For technical assistance with the webcast, please email at info@sbiaevents.com.