CRO – Clinical Trials (CT)

Clinical Trials (CT)

At BICS, we offer end-to-end Clinical Trial (CT) services as a committed and compliant Clinical Research Organization (CRO). With a strong foundation in ethics, science, and global quality standards, we support pharmaceutical, biotechnology, and medical device companies in conducting Phase I to Phase IV clinical trials across India and globally.

We understand that clinical research is a critical step in bringing safe and effective healthcare solutions to the world. That’s why our focus is on accuracy, patient safety, regulatory compliance, and timely delivery.

Our CRO Clinical Trial Services

  • Study Design & Protocol Development -
    Tailored trial designs that are scientifically sound and regulatory-ready.
  • Site Selection & Feasibility -
    Strategic site identification across India with experienced investigators and access to diverse patient populations.
  • Ethics & Regulatory Submissions -
    Complete support for ICMR, CDSCO, DCGI, and IEC submissions for faster approvals.
  • Project Management -
    End-to-end coordination ensuring smooth execution and timely milestones.
  • Site Monitoring & Data Management -
    On-ground monitoring with real-time reporting, clean data collection, and 100% GCP compliance.
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