ETHAN DROWER
CEO & Co-Founder, Cite Medical Solutions
Bio Info
Ethan Drower is the Co-Founder and Operating Partner of CiteMedical. With a strong commitment to revolutionize the European Union Medical Device Regulation (EU MDR) process, Ethan brings a unique blend of expertise to the table. His background as a trained software engineer, coupled with his partner's veteran experience in regulatory affairs and quality, has given birth to CiteMedical—a game-changer in the field and a company built fully remotely, while Ethan traveled to different countries, sailed around the Caribbean, and rode motorcycles in Mexico!
Ethan's journey is fueled by a passion to streamline and optimize the Literature Search and Review process, a critical pillar in the development of medical device companies' Clinical Evaluation Reports. At CiteMedical, their mission is crystal clear: deliver a high volume of carefully crafted Literature Reviews within timelines that empower companies to achieve their EU MDR goals swiftly and effectively. His knowledge of EU MDR/IVDR, clinical evaluation, literature review, and post-market surveillance has made him a sought-after authority in the industry.
For podcasts with audiences comprising medical device manufacturers, directors of regulatory affairs, and quality professionals, Ethan Drower is the ideal guest. His expertise and contributions at CiteMedical offer invaluable insights into the ever-evolving landscape of medical device regulations in the European Union. Book Ethan today to hear him share his vision, strategies, and innovative solutions that are driving transformation in the medical device industry. With Ethan, let's navigate the complex world of medical device regulations with confidence and expertise.
Previous Interviews
Mastering Medical Device
How a Regulatory Change Created a Product Opportunity with Ethan Drower
From Lab to Launch by Qualio
Modernizing the EUMDR Clinical Evaluation Report Process with Ethan Drower Co-founder of CiteMed
Success Made to Last Legends
Success Made to Last with Cite Med CEO and Co-founder Ethan Drower; solving pain point in EU medical world
Combinate Podcast - Combining Drugs and Devices
059 - Literature Review, EU MDR CER’s, and Being Problem Driven with Ethan Drower
Coffee with Closers
Content Is Profitable: Marketing Lessons From Software Developer Turned Entrepreneur | Ethan Drower
From Lab to Launch by Qualio
How CiteMed is Helping Medical Device Companies Bring Their Launches to Market Faster with Co-Founder, Ethan Drower
Let’s Talk Medtech
Let's Talk Medtech: Diving into the EU MDR with CiteMed
Global Medical Device Podcast powered by Greenlight Guru
Systematic Literature Review for EU MDR
Topic Suggestions
The most common notified body feedback on clinical evaluation & post market surveillance
Managing Large Medical Writing Teams: How to hire, train, and manage without going mad
Streamlining EU MDR compliance with on-demand clinical evaluation services
The benefits of expert-driven systematic literature reviews for EU MDR compliance
Navigating post-market surveillance challenges: Tips for a hassle-free process
How to efficiently organize audit responses in the EU MDR era
Harnessing the power of regulatory templates for EU MDR compliance
Continuous learning in regulatory affairs with training courses tailored to EU MDR requirements
Stay informed and stay compliant: The importance of regulatory news updates in EU MDR
Choosing Your EU MDR Compliance Path: Done for you, done with you, or do it yourself — What's best for your team?
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