|
IRB Management
The rules and regulations of institutional review boards vary amongst clinical trial sites. Let Fathom manage the numerous clinical trial sites by fulfilling all of the necessary paperwork required by each institution prior to patient enrollment.
Trial Planning and Execution
Successful evaluation of your device requires clear and concise protocols to ensure uniform usage across sites. Our experts are experienced in the creation and execution of clinical trial protocols and the management of multiple simultaneous international sites.
Data Analysis
Clinical trials result in a tremendous amount of data. We can biostatistically evaluate your data to ensure compliance with the end points of your clinical trial, and support the creation of a final report for submission to your regulatory agency.
|
|
