Support for Device Companies

We help you communicate data supporting your therapies’ efficacy.

Get professional help with clinical editing and publication services, literature reviews, and regulatory assistance for medical device companies.

We work with partners in medical, clinical, and regulatory affairs to write, analyze, and publicize data supporting your therapy’s efficacy. Whether you work in medical affairs, clinical research management, or research administration, Superior Medical Experts can help.

What sets us apart?

Our service is truly comprehensive. Everything in the research publication process a clinician does not have to do, we provide. We use a flexible, a la carte, customizable approach to get your medical device or therapy to market.


Clinical protocol editing and drafting


Study design/feasibility research


IRB submissions


Clinical trial registration (


Clinical study report editing and drafting


Statistical analysis


Regulatory letters, responses, and rationales



Manuscript drafting and submissions


Tables, graphs, and illustrations


Conference abstracts, posters, and slide decks


Post-market clinical follow-up (PMCF) reports


CER, 510(k), PMA, IDE editing and technical writing assistance


Whitepapers, Value Briefs, Product Blueprints, and other promotional materials


Translation services (Mandarin, Japanese, French, Spanish, and German)


Interested In Our Services? Reach out to Us!

Contact Us