For easy access to our site’s regulatory documents, electronic access is available through our Monitor Portal.
Request access to the portal by completing our request access form.
Once access has been granted from the administrator, click the login button below.
eDocs Portal provides Sponsors/CROs electronic access to those regulatory documents (Core Documents) that are common to all clinical trials, making regulatory document management more efficient and timely.
If you have any questions or concerns, please contact the site directly to resolve any issues.
Fields marked with * are required.