
Sign up to save your podcasts
Or
Why do the same types of problems show up again and again in FDA medical device inspections? In today’s episode, Mike Drues joins the podcast to talk about the FDA's Fiscal Year Report for 2022 Inspections and discusses the most common problems found during these inspections.
Recurring guest Mike Drues is the President of Vascular Sciences where he works to educate the industry and offers help to bring medical devices to market in the most effective way possible. Mike is a medical device professional possessing regulatory expertise who understands the ins and outs of the regulation systems in the medical device industry and is passionate about helping others better understand it as well.
Listen to the episode to learn more about the most common mistakes companies make that result in Form 483s, what companies can do to avoid these mistakes, and how you should be thinking about root cause analysis.
Some of the highlights of this episode include:“The emphasis should be on prevention, not correction.”
“I consider myself to be a medical device professional, and I do not use the word “professional” lightly. Along with it comes the responsibility, including knowing what the heck you’re doing.”
“What is the point of getting complaints or post-market surveillance or anything else if you’re not going to act on it?”
“I hate to say it, but we are the poster children for Einstein’s definition of insanity.”
Links:Mike Drues LinkedIn
Vascular Sciences
Etienne Nichols LinkedIn
Greenlight Guru Academy
MedTech Excellence Community
Greenlight Guru
4.8
9191 ratings
Why do the same types of problems show up again and again in FDA medical device inspections? In today’s episode, Mike Drues joins the podcast to talk about the FDA's Fiscal Year Report for 2022 Inspections and discusses the most common problems found during these inspections.
Recurring guest Mike Drues is the President of Vascular Sciences where he works to educate the industry and offers help to bring medical devices to market in the most effective way possible. Mike is a medical device professional possessing regulatory expertise who understands the ins and outs of the regulation systems in the medical device industry and is passionate about helping others better understand it as well.
Listen to the episode to learn more about the most common mistakes companies make that result in Form 483s, what companies can do to avoid these mistakes, and how you should be thinking about root cause analysis.
Some of the highlights of this episode include:“The emphasis should be on prevention, not correction.”
“I consider myself to be a medical device professional, and I do not use the word “professional” lightly. Along with it comes the responsibility, including knowing what the heck you’re doing.”
“What is the point of getting complaints or post-market surveillance or anything else if you’re not going to act on it?”
“I hate to say it, but we are the poster children for Einstein’s definition of insanity.”
Links:Mike Drues LinkedIn
Vascular Sciences
Etienne Nichols LinkedIn
Greenlight Guru Academy
MedTech Excellence Community
Greenlight Guru
177 Listeners
7,820 Listeners
30,894 Listeners
32,127 Listeners
66 Listeners
43,262 Listeners
1,042 Listeners
111,437 Listeners
56,158 Listeners
20 Listeners
5 Listeners
8,688 Listeners
34 Listeners
2,111 Listeners
3 Listeners