Your On-Demand Medical Writing and Research Team

Our software platform is the most efficient in the industry, but if you ever need an expert set of eyes to review, or crank out some projects, we’re here for you.

For Pharma, Medtech, or Research. Drop us a line.

Problems We Solve

Systematic Literature Review

Our specialty. Whether you need an EU MDR/IVDR Compliant Protocol, or a Meta-Analysis done to support an FDA Registered product, our review team is here to support, or take over.

Post Market Reporting and Vigilance

Post Market reporting goes far deeper than just literature review, our team can review adverse event databases, compile your complaints, and produce Audit-Ready reports for your medical device or drug.

Market Research and Meta-Analysis

Need to get a grip on the current literature for a particular procedure, compound, or indication? Our team can put together a comprehensive report of all available literature, analyzed and presented exactly how you need it.

What It’s Like
Working With
CiteMed

Our Team and Experience

Our team has been dedicated to medical writing, regulatory, and quality assurance in the Medical Device and Pharmaceutical industries for decades. A hand selected team of 15+ (with a few software engineers and data scientists thrown in for good measure) has seen it all.
Have a reporting need, or a particularly sticky problem to solve? Try us.

Read More About Our Trials and Tribulations