Global Medical Device Podcast powered by Greenlight Guru
Podcast autorstwa Greenlight Guru + Medical Device Entrepreneurs - Poniedziałki
416 Odcinki
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CDRH Proposed Guidance for FY 2023
Opublikowany: 22.12.2022 -
Future of the Emergency Use Authorization (EUA): COVID, Monkeypox & Beyond
Opublikowany: 15.12.2022 -
The Future of Healthcare & How We Get There
Opublikowany: 8.12.2022 -
What "Exempt" Means with Respect to Medical Devices & Regulatory
Opublikowany: 30.11.2022 -
Developing a Regulatory Strategy
Opublikowany: 23.11.2022 -
We Achieved ISO Certification! Now What?
Opublikowany: 17.11.2022 -
The Future of Reprocessed Used Medical Equipment
Opublikowany: 11.11.2022 -
The Importance of Cervical Cancer Screening in the U.S.
Opublikowany: 4.11.2022 -
Customer Discovery for Medical Device Companies
Opublikowany: 2.11.2022 -
EUA and the Impending Transition
Opublikowany: 26.10.2022 -
Common QMS Mistakes SaMD Companies Make
Opublikowany: 21.10.2022 -
Design Assurance: The Unsung Heroes of R&D
Opublikowany: 13.10.2022 -
Lessons from an Industry Leader: Playing the Long Game of MedTech
Opublikowany: 6.10.2022 -
7 Common 510(k) Mistakes and How to Avoid Them
Opublikowany: 29.09.2022 -
Best Practices for Clinical Evidence Management
Opublikowany: 22.09.2022 -
Building Your Regulatory Strategy for Commercialization
Opublikowany: 14.09.2022 -
Packaging Validation Best Practices
Opublikowany: 7.09.2022 -
Overcoming Submission Deficiencies due to Biocompatibility
Opublikowany: 1.09.2022 -
Does Your CAPA Process Need a CAPA?
Opublikowany: 24.08.2022 -
UDI and the Current State of Global Implementation
Opublikowany: 18.08.2022
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.
