Support for Drug and Device Companies
Communicate your device or therapy’s efficacy with ease
We assist with your medical writing needs (and more!) so that you can focus on development and testing.
Why choose us?
Our service is truly comprehensive. Everything in the research publication process that doesn’t require a clinician, we provide. We use a flexible, a la carte, customizable approach to get your medical device or therapy to market.
We provide professional clinical editing and publication services, literature reviews, and regulatory assistance. We work with experts in medical, clinical, and regulatory affairs to write about, analyze, and publicize data supporting your therapy or device. Whether you work in medical affairs, clinical research management, or research administration, Superior Medical Experts can help.
some of the many ways we can serve your business needs
Review our service categories to see how we help support novel therapies and devices. If you don’t see a service that addresses one of your needs, reach out to schedule a consultation!
- Clinical protocol editing and drafting
- Clinical study report editing and drafting
- Manuscript drafting and submissions
- Study design/feasibility research
- CER, 510(k), PMA, IDE editing and technical writing assistance
- Post-market clinical follow-up (PMCF) reportLiterature Reviewss
- Regulatory letters, responses, and rationales
- Literature Reviews
- IRB submissions
- Table, graph, and illustration creation
- Conference abstract, poster, and slide deck creation
- Whitepapers, Value Briefs, Product Blueprints, and other promotional materials
- Comprehensive Statistical Analysis
- Clinical trial registration (clinicaltrials.gov)
- Translation services for Select languages