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 setup - 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 of experienced expertise • 24*7 Data Backup • Archival facility • Fully developed SOPs (As per GCP) • Customized Monitoring Plans • Customised monitoring reports/checklists • Timely updates to sponsor • Dedicative Medical Monitor/Female Monitor for Female studies