31 min listen
Using the Bucket Method for Medical Device Risk Management w/ Mike Drues
FromGlobal Medical Device Podcast powered by Greenlight Guru
Using the Bucket Method for Medical Device Risk Management w/ Mike Drues
FromGlobal Medical Device Podcast powered by Greenlight Guru
ratings:
Length:
34 minutes
Released:
Nov 7, 2019
Format:
Podcast episode
Description
Risk management: It’s a topic that needs to be navigated carefully by medical device companies.
It’s been gaining a lot of traction in the industry, because some recent standards have focused on risk management.
Today’s guest has seen companies take their risk management plan directly from their design controls and paste them into their regulatory submission forms. This is not a correct way to approach risk management, because it gives an incomplete picture.
Mike Drues, the president of Vascular Sciences, has been a frequent guest on our show.
Not only do we listen to him, but the FDA and Health Canada do, too, because Mike works with these regulatory agencies in addition to working with medical device companies.
Today we’re talking about risk management. Mike has a three (plus one bonus) bucket approach to dealing with this important topic.
Some of the ideas that we discuss today include:
● Mike’s systematic approach to risk management: three “buckets” he uses when developing his plans.
● How to measure, track and present the probability of harm of not using the device.
● Mike’s thoughts on using FMEA as a tool.
● The problem with equating misuse as off-label use, and what the difference is.
● Mike’s solution for facing the problem of liability pertaining to off-label use of a device.
● Why it’s important not to become a slave to whatever tool(s) your company is using when dealing with risk management.
It’s been gaining a lot of traction in the industry, because some recent standards have focused on risk management.
Today’s guest has seen companies take their risk management plan directly from their design controls and paste them into their regulatory submission forms. This is not a correct way to approach risk management, because it gives an incomplete picture.
Mike Drues, the president of Vascular Sciences, has been a frequent guest on our show.
Not only do we listen to him, but the FDA and Health Canada do, too, because Mike works with these regulatory agencies in addition to working with medical device companies.
Today we’re talking about risk management. Mike has a three (plus one bonus) bucket approach to dealing with this important topic.
Some of the ideas that we discuss today include:
● Mike’s systematic approach to risk management: three “buckets” he uses when developing his plans.
● How to measure, track and present the probability of harm of not using the device.
● Mike’s thoughts on using FMEA as a tool.
● The problem with equating misuse as off-label use, and what the difference is.
● Mike’s solution for facing the problem of liability pertaining to off-label use of a device.
● Why it’s important not to become a slave to whatever tool(s) your company is using when dealing with risk management.
Released:
Nov 7, 2019
Format:
Podcast episode
Titles in the series (100)
What Device Makers Need to Know About Design Verification and Validation with Mike Drues: Here’s a question for our listeners: When it comes to making sure your medical devices are safe and effective, is it more important to find the right answers or to ask the right questions? In this episode of the Global Medical Device podcast, we are d... by Global Medical Device Podcast powered by Greenlight Guru