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About FDA’s Data Standards Program
114 - Discover Strategies for De-Risking Medical Device Development: FDA Consensus Standards
Closing Keynote: CDRH Updates
FDA-USP-AAM | D1S3 - Industry’s Engagement in USP’s Standards-Setting Process
Scientific Workshop: Next-Generation Sequencing for Adventitious Agent Detection in Biologics
US FDA Standards Overview
2021 CERSI Summit - Update from CDRH
Episode 003: Improving the Quality of Medical Devices - Cisco Vicenty, FDA Case for Quality Program
Decoding FDA's Standards for Regenerative Medicine
Common Rule Essentials for FDA CDRH Group
FDA CDER Regulatory Science: Improving Drug Review with Data Standards
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Last Updated: September 24, 2026
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Summary
The Food and Drug Administration ( On August 24, 2022, SCB hosted a webinar to discuss the recently released We've talked about problem solving techniques, we've talked about sense-making frameworks, we've talked about Jeff Shuren, MD, JD | Director, This session outlined ways industry can stay engaged with USP's Have a question for the speakers or panelists? Email your questions to OTPEvents@ Medical devices are a major contributor to the quality of life for many people. To ensure the quality of the medical devices, the ... The US Food and Drug Administration ( U.S. Department of Health and Human Services (HHS) | hhs.gov Twitter.com/HHSGov |