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We provide CRA's to Sponsors/CRO's
Clinical Research Associates
We provice experienced, qualified and trained CRA's to monitor clinical trial sites
Site Selection
We help in selection of sites as per the protocol and sponsor requirement. Clinical trial sites with all the facilities, experienced study staff and Experienced Investigators with good number of patient pool
Monitoring
Monitoring of sites and study documents during the study, preparing site for any regulatory audits, site close out and facilitating archival of study documents
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