Global Medical Device Podcast powered by Greenlight Guru

Ein Podcast von: Greenlight Guru's Jon Speer + Medical Device Entrepreneurs, Executives, Inventors & Consultants; R&D, Quality, Regulatory

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.

Our American listeners can also listen to Global Medical Device Podcast powered by Greenlight Guru at our American site

292 Folgen

Developing a Regulatory Strategy
Vom 2022-11-23

We Achieved ISO Certification! Now What?
Vom 2022-11-16
The Future of Reprocessed Used Medical Equipment
Vom 2022-11-10
The Importance of Cervical Cancer Screening in the U.S.
Vom 2022-11-04
Customer Discovery for Medical Device Companies
Vom 2022-11-02
EUA and the Impending Transition
Vom 2022-10-26
Common QMS Mistakes SaMD Companies Make
Vom 2022-10-20
Design Assurance: The Unsung Heroes of R&D
Vom 2022-10-13
Lessons from an Industry Leader: Playing the Long Game of MedTech
Vom 2022-10-06
7 Common 510(k) Mistakes and How to Avoid Them
Vom 2022-09-29
Best Practices for Clinical Evidence Management
Vom 2022-09-22
Building Your Regulatory Strategy for Commercialization
Vom 2022-09-14
Packaging Validation Best Practices
Vom 2022-09-07
Overcoming Submission Deficiencies due to Biocompatibility
Vom 2022-08-31
Does Your CAPA Process Need a CAPA?
Vom 2022-08-24
UDI and the Current State of Global Implementation
Vom 2022-08-17
The Changing Job Market & How It Affects Careers for MedTech Quality Professionals
Vom 2022-08-10
Digitizing your SaMD Testing
Vom 2022-08-03
Examining FDA’s Refusal to Accept (RTA) Policy and Guidance
Vom 2022-07-27
Guerilla Tactics for Quality Leadership
Vom 2022-07-20

292 Folgen

Developing a Regulatory Strategy

We Achieved ISO Certification! Now What?

The Future of Reprocessed Used Medical Equipment

The Importance of Cervical Cancer Screening in the U.S.

Customer Discovery for Medical Device Companies

EUA and the Impending Transition

Common QMS Mistakes SaMD Companies Make

Design Assurance: The Unsung Heroes of R&D

Lessons from an Industry Leader: Playing the Long Game of MedTech

7 Common 510(k) Mistakes and How to Avoid Them

Best Practices for Clinical Evidence Management

Building Your Regulatory Strategy for Commercialization

Packaging Validation Best Practices

Overcoming Submission Deficiencies due to Biocompatibility

Does Your CAPA Process Need a CAPA?

UDI and the Current State of Global Implementation

The Changing Job Market & How It Affects Careers for MedTech Quality Professionals

Digitizing your SaMD Testing

Examining FDA’s Refusal to Accept (RTA) Policy and Guidance

Guerilla Tactics for Quality Leadership