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 (clinicaltrials.gov)

 

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