C-Trials Global Inc.

Expertise in -Medical Monitoring -Clinical Trials Monitoring -Clinical Endpoint Study monitoring -Bioequivalence Study Monitoring -Patient Based PK Study Monitoring -Formulations and Development contract services -End to end Dossier submission -Complete CRO/Plant Set up -Audits(GCP, GLP, c-GMP) -Training(GCP, GLP, c-GMP) -Bio-analytical Consulting Why chose us • More than 500 CT/PKPD/BA/BE Studies monitored • More than 50 trainings and consulting programs conducted • More than 40 System and facility Audits • More than 20 GMP Audits • More than 10 Years experienced expertise • 24*7 Data Back up • Archival facility • Fully developed SOPs (As per GCP) • Customized Monitoring Plans • Customized Monitoring reports/Check lists • Timely updates to sponsor • Dedicative Medical Monitor/Female Monitor for Female studies