25 min listen
Modernizing the EUMDR Clinical Evaluation Report Process with Ethan Drower Co-founder of CiteMed
Modernizing the EUMDR Clinical Evaluation Report Process with Ethan Drower Co-founder of CiteMed
ratings:
Length:
20 minutes
Released:
Apr 15, 2022
Format:
Podcast episode
Description
Adopting EU MDR is either going to make or break some regulatory teams. With some major updates to EU MDR in the past couple years, the need for innovation and efficiency has never been greater for med device companies. We love hearing stories where experts in different industries come together to solve a massive problem and unlock potential for life-saving products. That's the story behind CiteMed where a software engineer and regulatory veteran came together to help med device companies with EU MDR and keep their products and new products in the market. Ethan Drower, co-founder of CiteMed made a streamlined process for a med device company’s clinical evaluation report documentation - which some medical writers spend hours even whole careers on. CiteMed's approach is modern and efficient. He’ll explain more the backstory and process in the show. CiteMed's top goal is to help companies get their medical products to market as quickly as possible all while maintaining state-of-the-art compliance with the European Commission regulations. Check out CiteMed's EU MDR templates and content on their website below.If EU MDR is on your mind, you’ll get a lot from what Ethan and the team at CiteMed is doing.About Ethan Drower and CiteMed:Ethan Drower is the Co-Founder and Operating Partner of CiteMed, which is revolutionizing the European Union Medical Device Regulation (EU MDR) process. Literature Search and Review is the cornerstone of medical device companies' Clinical Evaluation Report, and CiteMed has made this process more streamlined and optimized than ever. Ethan as a software engineer and his partner, a veteran in the regulatory space, started CiteMed to deliver a high volume of beautifully written and formatted Literature Reviews on timelines that will enable companies to meet their EU MDR goals. Show Notes:CiteMed website: https://citemedical.com/CiteMed EUMDR resources: https://www.citemedical.com/learn-eu-mdr/Ethan's LinkedIn: https://www.linkedin.com/in/ethandrower/Qualio WebsitePrevious episodes: https://www.qualio.com/from-lab-to-launch-podcastApply to be on the show: https://forms.gle/uUH2YtCFxJHrVGeL8Music by keldezQualio website:https://www.qualio.com/ Previous episodes:https://www.qualio.com/from-lab-to-launch-podcast Apply to be on the show:https://forms.gle/uUH2YtCFxJHrVGeL8 Music by keldez
Released:
Apr 15, 2022
Format:
Podcast episode
Titles in the series (100)
Unlock Funding with IP and Focusing Your Purpose. The inspiring story behind HAI Solutions with Nick Perrenoud. by From Lab to Launch by Qualio