Medical Writing Services

NCRA's Medical Writing Team produces medical and technical writing for all phases of your product's clinical research and development. For clinical trials, our capabilities range from producing the Clinical Investigator's Manual/Investigator's Brochure/Report of Prior Investigations through development of the protocol, to completing the final report.

NCRA’s writing group produces cohesive, integrated statistical/medical reports. We can fulfill your outsourcing needs by completing:

• Outstanding or delayed study final reports
• Investigational new drug application (IND) and new drug application (NDA) submissions
• Investigational device exemption (IDE), 510(K) and pre marketing approval (PMA) submissions
• International product licensing applications (PLA)