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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

FromFrom Lab to Launch by Qualio


Modernizing the EUMDR Clinical Evaluation Report Process with Ethan Drower Co-founder of CiteMed

FromFrom Lab to Launch by Qualio

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)

Stories from the front lines of life sciences. Hear how founders, investors, engineers, scientists, and quality experts are innovating to save lives. You’ll hear founders share their insights from launching and scaling their business, investors giving their outlook on funding, industry experts unfolding their latest insights and research, and quality professionals offering advice to navigate the regulatory maze and avoid audit pitfalls. We interview the brightest people in the life sciences industry specifically biotechnology, medical devices, healthcare, pharmaceuticals, software as a medical device (SaMD), contract service providers, and therapeutics. Episodes are about 20-30 minutes. Tune in and leave inspired to bring your life saving products to the world. Passionate about life sciences and want to be on the show? We’d love to chat. Please fill out this short application: https://forms.gle/Yp7uKnSXTCPtTdRcA