At C-Trials Global we believe transparency and flexibility are the keys to success when working with our clients. Our clients and the trials being conducted come in versatile shapes and sizes. We endeavor to meet our clients’ needs by being proactive and have created an environment that advances this approach with our teams. We believe people/clients are our greatest asset and understand that best performances come from individuals who know they are part of an esteemed team.
Why choose us
Experience with all phases of clinical trials (Phase II -IV) across multiple therapeutic areas, in paper and Electronic data environments
Highly experienced and responsive team with 20 years’ experience in the Pharmaceutical industry
More than 200 Sites, 250 PIs, more than 2000 Patients recruited till date
Worked with more than 50 ethics committees
Well trained and responsible staff (ICH-GCP, ICMR, New Drugs and Clinical Trials Rules, 2019 – CDSCO and FDA and other respective regulations)
Impeccable work record for delivery on time and with best quality
24X7 Data Backup
Archival Facility Available
End to end Clinical Trial services
Our Experiences
More than 20 Clinical Trials site development
More than 40 Registry local trials
More than 20 observational studies
Team of Expert with more than 20 years of experience
Independent CRCs support to more than 50 Trials
More than 50 CT Logistic support
More than 350 BA/BE Studies monitored
More than 720Bio-analytical Methods developed
More than 500 sponsor audits faced
More than 65 Regulatory Audits faced
More than 50 trainings and consulting programs conducted(GCP, GLP)