Global Medical Device Podcast powered by Greenlight Guru

A podcast by Greenlight Guru + Medical Device Entrepreneurs - Lunedì

416 Episodio

Integrating Business Elements into Your Product Development Process with Therese Graff
Pubblicato: 07/11/2019
Tips to Help You Prepare for an FDA Inspection
Pubblicato: 07/11/2019
What Device Makers Need to Know About Design Verification and Validation with Mike Drues
Pubblicato: 07/11/2019
Preparing Your Class II Device for the UDI Compliance Deadline with Gary Saner
Pubblicato: 07/11/2019
Dirty Devices and Reprocessing: Are New Design Change Rules On the Horizon?
Pubblicato: 07/11/2019
Insider Tips and Best Practices Regarding the 510(k) Submission Process from a Former FDA Reviewer
Pubblicato: 07/11/2019
Insights Into the New FDA 3D Printing Guidance & How It Impacts Med Device New Product Development
Pubblicato: 07/11/2019
How to Properly Use the FDA Pre-Submission Process and Why It's So Important with Mike Drues
Pubblicato: 07/11/2019
Tips & Pointers for Effective Internal Quality Audits with Kyle Rose
Pubblicato: 07/11/2019
Preparing for the Changes to the EU Medical Device and In-Virto Diagnostics Regulations
Pubblicato: 07/11/2019
Tips for Avoiding Problems with the First-In-Human Study Process with Mike Drues
Pubblicato: 07/11/2019
Understanding the New FDA Guidance on Changes to 510(k)
Pubblicato: 07/11/2019
What Devicemakers Need to Know about the FDA Pre-submission Process (Part Two)
Pubblicato: 07/11/2019
Zebra Medical Technologies: How a New Breed of Medical Device Companies Is Leveraging Technology
Pubblicato: 07/11/2019
Tips for Success When It Comes to IEC 60601 with Leo Eisner
Pubblicato: 07/11/2019
Using the Bucket Method for Medical Device Risk Management w/ Mike Drues
Pubblicato: 07/11/2019
2016 Medical Device Regulatory Trends Year in Review
Pubblicato: 07/11/2019
How Phagenesis Is Using Regulatory Affairs as They Develop a Treatment for Dysphagia
Pubblicato: 07/11/2019
What Devicemakers Need to Know About Medical Device Reporting (MDR)
Pubblicato: 07/11/2019
An Overview of What Device Makers Need to Know About CAPA
Pubblicato: 07/11/2019

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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.

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416 Episodio

Integrating Business Elements into Your Product Development Process with Therese Graff

Tips to Help You Prepare for an FDA Inspection

What Device Makers Need to Know About Design Verification and Validation with Mike Drues

Preparing Your Class II Device for the UDI Compliance Deadline with Gary Saner

Dirty Devices and Reprocessing: Are New Design Change Rules On the Horizon?

Insider Tips and Best Practices Regarding the 510(k) Submission Process from a Former FDA Reviewer

Insights Into the New FDA 3D Printing Guidance & How It Impacts Med Device New Product Development

How to Properly Use the FDA Pre-Submission Process and Why It's So Important with Mike Drues

Tips & Pointers for Effective Internal Quality Audits with Kyle Rose

Preparing for the Changes to the EU Medical Device and In-Virto Diagnostics Regulations

Tips for Avoiding Problems with the First-In-Human Study Process with Mike Drues

Understanding the New FDA Guidance on Changes to 510(k)

What Devicemakers Need to Know about the FDA Pre-submission Process (Part Two)

Zebra Medical Technologies: How a New Breed of Medical Device Companies Is Leveraging Technology

Tips for Success When It Comes to IEC 60601 with Leo Eisner

Using the Bucket Method for Medical Device Risk Management w/ Mike Drues

2016 Medical Device Regulatory Trends Year in Review

How Phagenesis Is Using Regulatory Affairs as They Develop a Treatment for Dysphagia

What Devicemakers Need to Know About Medical Device Reporting (MDR)

An Overview of What Device Makers Need to Know About CAPA