Clinical Research Department

The Clinical Research Department of Universal Hospital has been established with the primary objective of promoting ethical, high-quality, and scientifically rigorous clinical research. The department serves as a structured platform for conducting clinical trials, observational studies, and investigator-initiated projects that contribute to the advancement of medical knowledge and evidence-based patient care.

The department operates in accordance with national and international regulatory requirements, including the guidelines of the Central Drugs Standard Control Organization (CDSCO), the Indian Council of Medical Research (ICMR) National Ethical Guidelines, and the principles of Good Clinical Practice (GCP).

Our department supports physicians, investigators, and external collaborators in conducting high-quality research that aligns with regulatory standards and clinical best practices. We provide comprehensive services including:

  • Study feasibility assessments
  • Ethics and regulatory submissions
  • Coordination of clinical trials
  • Data collection and management
  • Training and guidance for clinical research staff

By integrating research into clinical practice, we aim to offer our patients access to cutting-edge therapies and contribute to evidence-based medicine.

If you have any query please feel free to contact us on 7283907585/ Universalhospital.crdsurat@gmail.com

We look forward to a healthy business relationship which not only will raise the bar for Clinical Research in India but also will help humanity at large.

Institutional Ethics Committee (IEC)

The Institutional Ethics Committee (IEC) at our hospital is an independent body responsible for safeguarding the rights, safety, and well-being of individuals participating in clinical research.

The IEC reviews all research proposals involving human participants to ensure they are conducted in accordance with ethical principles, national regulations (including ICMR guidelines), and international standards such as Good Clinical Practice (GCP).

Key responsibilities of the IEC include:

  • Reviewing and approving research protocols
  • Ensuring informed consent is properly obtained
  • Monitoring ongoing research for ethical compliance
  • Protecting vulnerable populations involved in research

The committee is composed of medical experts, legal and ethical professionals, and community representatives, ensuring a balanced and transparent review process. No clinical research may begin at our hospital without prior approval from the IEC.

Universal Hospital Institutional Ethics Committee SURAT.

It is Registered under the DCGI with Registration number ECR/2124/Inst/GJ/2025.

If you have any query please feel free to contact us on 7283907585/ Universalhospital.crdsurat@gmail.com