Global Medical Device Podcast powered by Greenlight Guru
Podcast autorstwa Greenlight Guru + Medical Device Entrepreneurs - Poniedziałki
416 Odcinki
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How Surgical Innovation Associates Found the Benefit of Quality Beyond Just Compliance
Opublikowany: 7.11.2019 -
Significant Risk vs. Nonsignificant Risk Devices - What's the Difference?
Opublikowany: 7.11.2019 -
How SimplicityMD Is Leveraging Technology to Help Get Their Devices to Market Faster
Opublikowany: 7.11.2019 -
How FDA Interacts with Medical Devices When They Are Imported into the US
Opublikowany: 7.11.2019 -
Understanding the Connection Between Complaints, CAPAs, and MDRs
Opublikowany: 7.11.2019 -
The Intersection of Medical Device Usability and Risk Management
Opublikowany: 7.11.2019 -
When Design Inputs Go Wrong + Design Your Label Like You Design Your Device
Opublikowany: 7.11.2019 -
Understanding FDA’s Proposed Conformity Assessment Pilot Program
Opublikowany: 7.11.2019 -
Understanding the Difference Between a General Wellness Device and a Regulated Medical Device
Opublikowany: 7.11.2019 -
Comparing FDA Submission Types: 510(k) vs. De Novo vs. 513(g) vs. Pre-Submission
Opublikowany: 7.11.2019 -
Why the 510(k) Process Is So Stressful & How You Can Help Streamline It
Opublikowany: 7.11.2019 -
How Competitive Regulatory Strategy Differs from Regular Regulatory Strategy
Opublikowany: 7.11.2019 -
Lessons to Be Learned From Recent FDA Inspections
Opublikowany: 7.11.2019 -
How Process Excellence Leads to Product Excellence
Opublikowany: 7.11.2019 -
Common Mistakes That Can Tank Your FDA 510(k) Submission
Opublikowany: 7.11.2019 -
Understanding How to Use Real-World Evidence for Medical Device Regulatory Decisions
Opublikowany: 7.11.2019 -
Challenges with Applying Risk Management Throughout the Manufacturing Process
Opublikowany: 7.11.2019 -
An Overview of What Medical Device Developers Need to Know About Human Factors
Opublikowany: 7.11.2019 -
Evaluating FDA’s “New” Proposed Fast-Track Alternative Approach to the 510(k) Pathway
Opublikowany: 7.11.2019 -
What Substantial Equivalence Means as It Applies to 510(k)'s & Why It's So Important
Opublikowany: 7.11.2019
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.
