UP-IMRAS

Uttar Pradesh Promote Pharma Council

UP-IMRAS (Integrated Medical Research Application System) is a comprehensive digital platform developed to strengthen the clinical research ecosystem across Uttar Pradesh by providing a unified, paperless, and transparent system for medical research administration. The platform enables institutions, investigators, sponsors, and ethics committees to collaborate through a single-window application for research feasibility, clinical study approvals, grant management, and clinical trial registration.

The system streamlines the complete research lifecycle; from institutional registration and investigator profiling to ethics committee approvals, compliance monitoring, and study tracking. UP-IMRAS promotes transparency, regulatory compliance, digital governance, and efficient coordination among all stakeholders, accelerating high-quality medical research and innovation across the state.

90+
Registered Institutions
10+
Research Sponsors
02+
Ongoing Clinical Trials
2,736+
Registered Investigators

Key Benefits

Single-window digital platform for clinical research management across Uttar Pradesh.

Paperless application and approval process for research studies and clinical trials.

Faster research approvals through digitized workflows and automated processing.

Secure and verified registration for institutions, investigators, and sponsors.

Enhanced transparency and regulatory compliance throughout the research lifecycle.

Streamlined grant and research fund management with centralized monitoring.

Real-time tracking of clinical studies, approvals, and research progress.

Promotes high-quality medical research, innovation, and collaboration across the state.

Key Features

  • Single-window application system for research proposals and clinical studies.
  • Verified registration and profile management for institutions, investigators, and sponsors.
  • Digitized Ethics Committee workflow for online review and approvals.
  • Clinical trial registration with end-to-end lifecycle management.
  • AI-enabled compliance validation and quality assurance checks.
  • End-to-end grant and research fund management system.
  • Real-time dashboards for study monitoring, analytics, and status tracking.
  • Secure role-based access with centralized document management and automated digital workflows.

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