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.