<ul><li>Responsible for overall conduct of GLP compliance studies as per OECD Principles of Good Laboratory Practice.</li><li>To assist in preparation of study plan and any amendments to the study plan.</li><li>To follow study plans and amendments and Standard Operating Procedures for the conduct of study.</li><li>To record all the raw data promptly and legibly.</li><li>To assist in compilation of results and preparation of study report.</li><li>To prepare the study plan, the final report, raw data and supporting material after completion (including termination) of the study, for archival.</li><li>To maintain the instrument calibration records, logbooks related to the section.</li></ul><p>&nbsp;</p>

Study Personnel Genetic Technology