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FDA | Small Business and Industry Assistance (SBIA)
Regulatory Education for Industry (REdI)
Annual Conference 2024
Innovation in Medical Product Development
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Hybrid
May 29 – 30 | 8:30 AM - 4:30 PM ET
In-Person at The Hotel @ the University of Maryland College Park, MD
Online via Adobe Connect
TRACKS WILL OFFER AN OPPORTUNITY FOR 1:1 QUESTIONS FOR ONSITE ATTENDEES
Learn directly from the FDA’s regulatory experts in medical product centers: drugs, devices, and biologics. This course is designed to provide participants with a strong, basic foundation in the FDA’s regulatory requirements, and also create awareness of current activities.
💡 Test Your Knowledge with our LinkedIn Polls
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🔹 AND DON'T FORGET
Learn more about the new CDER Center for Clinical Trial Innovation (C3TI). C3TI is a central hub that supports innovative approaches to clinical trials to improve the efficiency of drug development. C3TI aims to promote existing CDER programs and spur future innovation activities through enhanced communication and collaboration, with the ultimate goal of accelerating the developing of safe and effective new drugs.
CONTINUING EDUCATION (CE)
Real-time participation is required for the certificate of attendance, which can be used in support of CEs for the following professional organizations: RAPS, SOCRA, SQA, and ACRP. Certificates are only available during the two weeks post-event. For more information, see details on our webpage.
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The Small Business and Industry Assistance (SBIA) program in the Center for Drug Evaluation and Research provides guidance, education and updates for regulated industry.
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