30 min listen
Helping Prepare Biomedical Engineers Entering the Workforce
FromGlobal Medical Device Podcast powered by Greenlight Guru
Helping Prepare Biomedical Engineers Entering the Workforce
FromGlobal Medical Device Podcast powered by Greenlight Guru
ratings:
Length:
33 minutes
Released:
Nov 7, 2019
Format:
Podcast episode
Description
Students offer hope for our future. They will be developing products that can save our lives, or at least improve our quality of life. We need to give them as much guidance and advice as possible.
On today’s episode, we have Associate Professor Andrew DiMeo, who shares his mission and what he is trying to do with the biomedical program at the University of North Carolina and North Carolina State University.
Some of the highlights of the show include:
● Andrew’s biomedical product development course is based on quality and regulatory.
● It is possible to be creative and innovative in a restrictive regulated environment, like biomedical engineering.
● Some people believe regulations/controls and the status quo prevent them from getting things done.
● The reasons why controls and regulations are necessary.
● How to prepare biomedical engineers entering the workforce.
● Andrew teaches students by using a real-life medical system.
● Regulations should be kept simple to avoid being too restrictive.
● Andrew describes a siloed world where collaboration is key.
On today’s episode, we have Associate Professor Andrew DiMeo, who shares his mission and what he is trying to do with the biomedical program at the University of North Carolina and North Carolina State University.
Some of the highlights of the show include:
● Andrew’s biomedical product development course is based on quality and regulatory.
● It is possible to be creative and innovative in a restrictive regulated environment, like biomedical engineering.
● Some people believe regulations/controls and the status quo prevent them from getting things done.
● The reasons why controls and regulations are necessary.
● How to prepare biomedical engineers entering the workforce.
● Andrew teaches students by using a real-life medical system.
● Regulations should be kept simple to avoid being too restrictive.
● Andrew describes a siloed world where collaboration is key.
Released:
Nov 7, 2019
Format:
Podcast episode
Titles in the series (100)
Insider Tips and Best Practices Regarding the 510(k) Submission Process from a Former FDA Reviewer: One important piece of documentation that medical device companies rely on to get them through the regulatory process is the premarket notification 510(k). Since the FDA will refuse to accept submissions that are missing the appropriate documentation... by Global Medical Device Podcast powered by Greenlight Guru