CEO & Co-Founder, Cite Medical Solutions

Ethan Drower

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

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

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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