Global Medical Device Podcast powered by Greenlight Guru
A podcast by Greenlight Guru + Medical Device Entrepreneurs - Mondays
416 Episodes
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How Surgical Innovation Associates Found the Benefit of Quality Beyond Just Compliance
Published: 11/7/2019 -
Significant Risk vs. Nonsignificant Risk Devices - What's the Difference?
Published: 11/7/2019 -
How SimplicityMD Is Leveraging Technology to Help Get Their Devices to Market Faster
Published: 11/7/2019 -
How FDA Interacts with Medical Devices When They Are Imported into the US
Published: 11/7/2019 -
Understanding the Connection Between Complaints, CAPAs, and MDRs
Published: 11/7/2019 -
The Intersection of Medical Device Usability and Risk Management
Published: 11/7/2019 -
When Design Inputs Go Wrong + Design Your Label Like You Design Your Device
Published: 11/7/2019 -
Understanding FDA’s Proposed Conformity Assessment Pilot Program
Published: 11/7/2019 -
Understanding the Difference Between a General Wellness Device and a Regulated Medical Device
Published: 11/7/2019 -
Comparing FDA Submission Types: 510(k) vs. De Novo vs. 513(g) vs. Pre-Submission
Published: 11/7/2019 -
Why the 510(k) Process Is So Stressful & How You Can Help Streamline It
Published: 11/7/2019 -
How Competitive Regulatory Strategy Differs from Regular Regulatory Strategy
Published: 11/7/2019 -
Lessons to Be Learned From Recent FDA Inspections
Published: 11/7/2019 -
How Process Excellence Leads to Product Excellence
Published: 11/7/2019 -
Common Mistakes That Can Tank Your FDA 510(k) Submission
Published: 11/7/2019 -
Understanding How to Use Real-World Evidence for Medical Device Regulatory Decisions
Published: 11/7/2019 -
Challenges with Applying Risk Management Throughout the Manufacturing Process
Published: 11/7/2019 -
An Overview of What Medical Device Developers Need to Know About Human Factors
Published: 11/7/2019 -
Evaluating FDA’s “New” Proposed Fast-Track Alternative Approach to the 510(k) Pathway
Published: 11/7/2019 -
What Substantial Equivalence Means as It Applies to 510(k)'s & Why It's So Important
Published: 11/7/2019
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.