Role of AtlasCRo regarding regulatory support in clinical researches;
- ♦ Preparation of study files,
- ♦ Conduct to prepare the Ethics Committee & Regulatory Authorities submissions,
- ♦ Follow up applications,
- ♦ Contacting Ethics Committee & Regulatory Authorities for study purposes,
- ♦ Conduct to prepare Advers Event submissions,
- ♦ Notification of Ethics Committee & Ministry of Health about new Clinical Site Coordinator delegations into the clinical trials.