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From Data to Approval: GCP ClinPlus Accelerates OT-702 with Al-Powered Execution

From Data to Approval: GCP ClinPlus Accelerates OT-702 with Al-Powered Execution
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    GCP ClinPlus is honored to have been the CRO partner for OcuMension’s anti-VEGF drug OT-702, delivering comprehensive data management, statistical programming, and biostatistics support throughout its development. Our collaboration contributed to the therapy’s successful NMPA approval for treating neovascular age-related macular degeneration (nAMD) and diabetic macular edema (DME).


    How GCP ClinPlus Ensured High-Quality Delivery with AI & Data Science:


    ✓ Implemented an AI-integrated analytical framework to strengthen statistical inference and regulatory alignment
    ✓ Complied with international standards, maintaining complete data traceability and end-to-end quality control
    ✓ Devoted over 6,922 hours, with a 95-member expert team supporting 13 regulatory submissions
    ✓ Supported 210+ successful product approvals, demonstrating proven expertise in innovative drug development


    Partner with GCP ClinPlus to advance your drug’s pathway with data intelligence and global-quality execution.


    Contact us: global@gcp-clinplus.com

    References

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