Review of laboratory reports, ECGs and X-ray reports.
Preparation of selected list of volunteers in screening.
Obtaining written consent form the volunteers for a study.
Performing clinical examination and inclusion / exclusion criteria of volunteers during study conduct.
Monitoring of subjects during study conduct and providing necessary care.
Supervision of dose administration of subjects during the course of study.
Management of adverse events during the study and providing support to PI/CI./li>
Review of post-study laboratory reports.
Marinating sufficient medical / clinical supplies in the ICU and providing necessary training to study staff.
Review of literature and provide necessary support to PI for ensuring the safety of subjects.
Supervision of ICU and ambulance.
Providing necessary training to staff for ensuring the subject's safety.
Quality compliance in performing the activities.
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