23 min listen
The 100th Episode: A Few of My Favorite Moments
FromGlobal Medical Device Podcast powered by Greenlight Guru
The 100th Episode: A Few of My Favorite Moments
FromGlobal Medical Device Podcast powered by Greenlight Guru
ratings:
Length:
12 minutes
Released:
Nov 7, 2019
Format:
Podcast episode
Description
Drumroll, please. It’s time to celebrate the 100th episode of the Global Medical Device Podcast!
Jon Speer, 2-series podcast host, VP of QA/RA and founder of Greenlight Guru, reflects on some of his favorite moments and highlights through the years. “I’m a product development nerd. I’m a design control nerd. I geek out when I get to talk to some folks.”
Some of the highlights of the show include:
● Human Factors: Mary Beth Privitera and Bryant Foster
● Design Controls and Product Development: David Amor, Mike Fisher, and Scott Phillips
● Regulatory Testing and Safety: Leo Eisner
● Regulatory Affairs and Strategies: Allison Komiyama
● FDA Case for Quality Pilot Program: George Zack
● Device Marketing Authorization and Facility Registration: Jim Gianoutsos
● Preparing Biomedical Engineers Entering Workforce: Andrew DiMeo
● Most Popular and Frequent Guest: Mike Drues of Vascular Sciences
Jon Speer, 2-series podcast host, VP of QA/RA and founder of Greenlight Guru, reflects on some of his favorite moments and highlights through the years. “I’m a product development nerd. I’m a design control nerd. I geek out when I get to talk to some folks.”
Some of the highlights of the show include:
● Human Factors: Mary Beth Privitera and Bryant Foster
● Design Controls and Product Development: David Amor, Mike Fisher, and Scott Phillips
● Regulatory Testing and Safety: Leo Eisner
● Regulatory Affairs and Strategies: Allison Komiyama
● FDA Case for Quality Pilot Program: George Zack
● Device Marketing Authorization and Facility Registration: Jim Gianoutsos
● Preparing Biomedical Engineers Entering Workforce: Andrew DiMeo
● Most Popular and Frequent Guest: Mike Drues of Vascular Sciences
Released:
Nov 7, 2019
Format:
Podcast episode
Titles in the series (100)
Preparing Your Class II Device for the UDI Compliance Deadline with Gary Saner: If you are part of an organization developing or producing Class II medical devices, you should know that on September 24, 2016, your UDI submissions are due to the FDA. “I don’t mean to scare anyone, but we only have 78 working days left.” - Gary San... by Global Medical Device Podcast powered by Greenlight Guru