Why choose us

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.

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    Experience with all phases of clinical trials (Phase II -IV) across multiple therapeutic areas, in paper and Electronic data environments

  • conversations-4872_af60b258-251e-41af-b238-dfb706d7b3d4
    Highly experienced and responsive team with 20 years’ experience in the Pharmaceutical industry

  • diploma-2983_a6bb0b64-dbc1-431e-ac00-a83597982a0
    More than 200 Sites, 250 PIs, more than 2000 Patients recruited till date

  • messaging-app-4876_473fc710-9ecc-4785-9e78-8c9f00ae9498
    Worked with more than 50 ethics committees

  • flag-2979_1fd1d414-4b4f-4887-a94a-493ba8e0b0c7
    Well trained and responsible staff (ICH-GCP, ICMR, New Drugs and Clinical Trials Rules, 2019 – CDSCO and FDA and other respective regulations)

  • happy-emoji-2947_45d5bb03-c67d-4e73-a316-a5e7f4a9f2f7
    Impeccable work record for delivery on time and with best quality

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    24X7 Data Backup

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    Archival Facility Available

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    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)