Technical Writing

Documentation, analysis, interpretation and reporting of results of nonclinical medical device safety and efficacy studies in the form of interim or final GLP or feasibility reports, to the detail required by the client.

The Study Directors will summarize in report or verbal format results of feasibility studies to assist in further fund raising.

Create study protocols.

Organize and write manuscripts for peer-review journals.

Prepare Animal Care and Use Committee (IACUC) protocols.

Draft response letters of concerns from governing regulatory bodies and potential founding groups.