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CDRH
0:16:03
How is CDRH Structured?
5:41:06
REdI Annual Conference 2024: CDRH (Devices) Innovation in Medical Product Development (Day 1 of 2)
0:06:16
What is CDRH doing to accelerate the regulatory pathway for innovative medical technologies?
0:45:06
Conversation with Troy Tazbaz, Director of Digital Health at FDA's CDRH
6:52:20
REdI Annual Conference 2024: CDRH (Devices) Innovation in Medical Product Development (Day 2 of 2)
0:16:18
How is My Medical Device Classified?
0:02:53
Research Happens Here: The Office of Science and Engineering Laboratories within CDRH
0:12:13
CDRH Medical Imaging and Imaging Science Research
0:01:34
How is CDRH encouraging more US-based first-in-human studies?
0:11:30
Finally FDA CDRH releases an FDA eSTAR draft guidance for the eSTAR 510(k) templates
0:28:50
Closing Keynote: CDRH Updates
0:18:57
2021 CERSI Summit - Update from CDRH
0:52:39
A Roadmap for Medical Devices: From Innovative Ideas to the U.S. Market
0:55:14
FDA | NIH: Regulatory Do’s and Don’ts: Tips from FDA – CDRH Segment
0:17:43
Case Study: How is My Medical Device Classified?
0:34:01
RDM Workshop: Regulatory Guidance & Evidentiary Principles for DHT Development-Bakul Patel, FDA/CDRH
0:19:43
Update on CDRH Quality Pilot
0:59:16
MDICx Update on CDRH Patient Centered Initiatives
0:28:49
2016 MDIC Annual Public Forum: Dr. Jeff Shuren, Director CDRH
1:17:32
2020 MDIC Annual Public Forum-CDRH Town Hall (EXTENDED VERSION)
1:07:12
FDA's CDRH: Accelerating Upstream Medical Device Innovation
0:58:46
MDICx Series: July 30th: Patient Preference Framework & CDRH Guidance
0:02:28
FDA CDRH Increasing Medical Device Inspections
0:01:14
Collaborative Communities on Medical Devices
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