Cdrh

How is CDRH Structured?

U.S. Food and Drug Administration

REdI Annual Conference 2024: CDRH (Devices) Innovation in Medical Product Development (Day 2 of 2)

U.S. Food and Drug Administration

REdI Annual Conference 2024: CDRH (Devices) Innovation in Medical Product Development (Day 1 of 2)

U.S. Food and Drug Administration

What is CDRH doing to accelerate the regulatory pathway for innovative medical technologies?

Stanford Biodesign

Conversation with Troy Tazbaz, Director of Digital Health at FDA's CDRH

Structure of FDA/CDRH

Stanford Biodesign

From Mammograms to Microwaves - FDA's Center for Devices and Radiological Health | Researching FDA

U.S. Food and Drug Administration

How is My Medical Device Classified?

U.S. Food and Drug Administration

Research Happens Here: The Office of Science and Engineering Laboratories within CDRH

U.S. Food and Drug Administration

FDA | NIH: Regulatory Do’s and Don’ts: Tips from FDA – CDRH Segment

U.S. Food and Drug Administration

CDRH Katie O'Callaghan on when patient preference information is useful

MDIC - Medical Device Innovation Consortium

RDM Workshop: Regulatory Guidance & Evidentiary Principles for DHT Development-Bakul Patel, FDA/CDRH

Foundation for the National Institutes of Health

Finally FDA CDRH releases an FDA eSTAR draft guidance for the eSTAR 510(k) templates

Medical Device Academy

CDRH Medical Imaging and Imaging Science Research

UCSF-Stanford CERSI

CDRH vs. CDER

Stanford Biodesign

How is CDRH encouraging more US-based first-in-human studies?

Stanford Biodesign

Closing Keynote: CDRH Updates

MDIC - Medical Device Innovation Consortium

CDRH Katie O'Callaghan on the draft CDRH Patient Preference guidance

MDIC - Medical Device Innovation Consortium

2021 CERSI Summit - Update from CDRH

UCSF-Stanford CERSI