The first step toward activation of a particular clinical trial by a Participating Organization is to have all study personnel complete the following sets of roster documents. Our goal is to ensure the highest possible levels of competency and dedication to patient safety.
The attached packet includes complete instructions plus all but three of the required forms. Please open, download, complete, and print all needed forms. Contact us anytime if you have any questions.
Once the roster documents are received and processed by CPN's Operations Office, each individual will be issued a username and password that will provide access to the "Members Only" section of this website. At the same time, the Principal Investigator and Study Coordinator can work together to complete all of the regulatory documentation necessary for site activation. Operations Office personnel will provide instructions and assistance with this process.