<ul><li>Handling &amp; monitoring adverse event and serious adverse event.</li><li>Physibility of clinical study Project.</li><li>To communicate with Ethics Committee for review of Study Protocol.</li><li>Evaluate of screening and safety assessment report.</li><li>To ensure safety and well being of the subject.</li><li>To evaluate and ensure accountability of investigational products.</li><li>Ensure written informed consent is obtained from all study subjects.</li><li>Management of ICU.<br>&nbsp;</li></ul>

Principal Investigator-Clinical Research (Male)