CDRH

How is CDRH Structured?

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

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

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

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

How is My Medical Device Classified?

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

CDRH Medical Imaging and Imaging Science Research

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

Finally FDA CDRH releases an FDA eSTAR draft guidance for the eSTAR 510(k) templates

Closing Keynote: CDRH Updates

2021 CERSI Summit - Update from CDRH

A Roadmap for Medical Devices: From Innovative Ideas to the U.S. Market

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

Case Study: How is My Medical Device Classified?

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

Update on CDRH Quality Pilot

MDICx Update on CDRH Patient Centered Initiatives

2016 MDIC Annual Public Forum: Dr. Jeff Shuren, Director CDRH

2020 MDIC Annual Public Forum-CDRH Town Hall (EXTENDED VERSION)

FDA's CDRH: Accelerating Upstream Medical Device Innovation

MDICx Series: July 30th: Patient Preference Framework & CDRH Guidance

FDA CDRH Increasing Medical Device Inspections

Collaborative Communities on Medical Devices