Global Medical Device Podcast powered by Greenlight Guru
En podkast av Greenlight Guru + Medical Device Entrepreneurs
Kategorier:
368 Episoder
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#346: FDAs eSTAR Program
Publisert: 30.11.2023 -
#345: Using AI In MedTech
Publisert: 22.11.2023 -
#344: Becoming an Advisor to a Medical Device Company
Publisert: 16.11.2023 -
#343: Recent FDA Draft Guidances
Publisert: 9.11.2023 -
#342: Planning an FDA Submission
Publisert: 2.11.2023 -
#341: What NOT to say to FDA
Publisert: 25.10.2023 -
#340: LDTs & the FDAs Proposed Ruling
Publisert: 19.10.2023 -
#339: UDI and the State of EUDAMED
Publisert: 12.10.2023 -
#338: Site Selection for Clinical Trials
Publisert: 6.10.2023 -
#337: Moving MedTech Forward - The Past, Present & Future of Greenlight Guru
Publisert: 21.9.2023 -
#336: From Academia to FDA Clearance (True Quality Roadshow - Boston)
Publisert: 14.9.2023 -
#335: Accelerating SaMD Development in a Compliant Agile way
Publisert: 8.9.2023 -
#334: MedTech Funding and Preparing for Due Diligence
Publisert: 31.8.2023 -
#333: Exploring Breakthrough Device Designation
Publisert: 25.8.2023 -
#332: Regulatory Strategy and the Advantage of Diversity in MedTech
Publisert: 17.8.2023 -
#331: 28 Days To Save The World: Lessons Learned from a Pandemic Month of Supply Chain Issues
Publisert: 10.8.2023 -
#330: 3P510k: What Is a 510k 3rd Party Review, and What are the Benefits?
Publisert: 3.8.2023 -
#329 The Right Way to Start a QMS: When, How, & What
Publisert: 27.7.2023 -
#328 FDA Guidance on Artificial Intelligence (AI) in Medical Devices
Publisert: 20.7.2023 -
#327 Understanding the ROI of an eQMS
Publisert: 11.7.2023
The Global Medical Device Podcast, powered by Greenlight Guru, is where today's brightest minds in the medical device industry go to get their most useful and actionable insider knowledge, direct from some of the world's leading medical device experts and companies.