29 min listen
How Human Factors Impact Your Medical Device
FromGlobal Medical Device Podcast powered by Greenlight Guru
How Human Factors Impact Your Medical Device
FromGlobal Medical Device Podcast powered by Greenlight Guru
ratings:
Length:
43 minutes
Released:
Nov 7, 2019
Format:
Podcast episode
Description
Human factors can be a tricky topic that creates confusion, especially when it comes to medical devices. On today’s episode, we have Mike Drues, president of Vascular Sciences, to help us dive deeper into nuances of human factors.
The root cause for human factors related to medical devices is the watershed moment with infusion pumps that happened about 10 years ago.
Did you know that infusion pumps are one of the most often recalled medical devices for safety reasons? This has led to rigorous testing for all medical devices. But despite lessons learned, infusion pumps are still being recalled today.
SOME OF THE HIGHLIGHTS OF THE SHOW INCLUDE:
-Where human factors testing requirements come from.
-The importance of being proactive, observing, and learning when researching medical device issues.
-Why the lines between a clinical trial and usability/human factor study are blurry.
-Whether to require users to read instructions before using a product or participating in a study.
-The two steps needed to create a human factors/usability study.
-Human factor testing differences for devices used by medical professionals vs. patients.
-Human factors required after going to market.
-Combination products are popular, but deconstruct a product’s components to identify usability issues and understand the intent of regulations.
The root cause for human factors related to medical devices is the watershed moment with infusion pumps that happened about 10 years ago.
Did you know that infusion pumps are one of the most often recalled medical devices for safety reasons? This has led to rigorous testing for all medical devices. But despite lessons learned, infusion pumps are still being recalled today.
SOME OF THE HIGHLIGHTS OF THE SHOW INCLUDE:
-Where human factors testing requirements come from.
-The importance of being proactive, observing, and learning when researching medical device issues.
-Why the lines between a clinical trial and usability/human factor study are blurry.
-Whether to require users to read instructions before using a product or participating in a study.
-The two steps needed to create a human factors/usability study.
-Human factor testing differences for devices used by medical professionals vs. patients.
-Human factors required after going to market.
-Combination products are popular, but deconstruct a product’s components to identify usability issues and understand the intent of regulations.
Released:
Nov 7, 2019
Format:
Podcast episode
Titles in the series (100)
An Insider’s Look at the Changes Coming in ISO 13485:2016 with Mark Swanson: Did you know ISO 13485 has been revised and approved in 2016? And is going to be published later this month. The quality management standard we’ve all grown to know is now being updated, and we’ll explain more on this episode of the Global Medical De... by Global Medical Device Podcast powered by Greenlight Guru