Site Activation and Submission

Service Details

For the successful execution of a clinical trial, it is essential to carefully select sites and ensure their seamless integration into the process. Through our Site Activation and Submission, we facilitate the smooth inclusion of sites, handle the submission of necessary applications, and complete all approval processes. This ensures that clinical trials commence without delays, that sites are efficiently integrated, and that the process progresses successfully.

Scope of Our Services:

• Submission to Local Authorities

To include sites in the study, we obtain the necessary approvals from relevant local authorities and ensure that the entire process runs smoothly and without omissions.

• Preparation of Required Documents

All necessary documents are prepared in accordance with regulatory requirements for clinical research and submitted to the appropriate authorities.

• Site Initiation

Once all preparatory steps are completed, the clinical trial is officially initiated at the designated site.