Southern Clinical Trials Group Ltd
Our Advantage
- 6 clinical trial sites across New Zealand
- Quick and efficient start-up processes
- Centralised contract and budget negotiations. (One budget for all sites)
- TransCelerate attested GCP certification
- Online training portal for the delivery, tracking and reporting of training
- Robust quality assurance program
- Standardised SOPs for all clinical trial sites
- Extensive Lead IRB experience
- Dedicated recruitment capabilities
- Electronic access to common regulatory documents
Monitor Portal
For easy access to our site’s regulatory documents, electronic access is available through our Monitor Portal.
- Site Profile Forms
- CVs
- Medical Licenses
- Professional Indemnity
- Calibration Records
- SOPs
- Training Records
- Temperature Logs
Once access has been granted from the administrator, click the login button below.
Services
eDocs Portal Access Request Form
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.
Process
- On submission of the eDocs Portal Access Request Form, a notification is sent to the site’s administrator to create an account for you on the eDocs. (Please note that this is a manual process done by the administrator; therefore it may not be processed immediately.)
- Once the account has been set up by the administrator, you will receive a notification from eDocs with your login credentials
- Login into eDocs with the credentials provided to you.
If you have any questions or concerns, please contact the site directly to resolve any issues.
Fields marked with * are required.