Bio Scientific Research Laboratories (BIOSRL)

Review of pre-study file, during study and post study files, vaccutainer/vial labels, log books, completed ICF and CRFs in timely manner Ensuring that all staff involved in the study is trained in protocol Ensure that all the activities are been done as per protocol ,SOP s and GCP Assessing in pharmacy related activities (like Acceptance, labeling, dispensing, reconciliation and storage of IP s) Online monitoring and taking print of the temperature record from the software Providing study related information to the Ethics Committee, Contracted hospitals and Insurance company Preparation of study up- after completion of the study and send it to technical Documentation Preparation of Statistical up- and send it to the respective person Review clinical report