Role of AR CRO 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.