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With RM 1 billion generated in national gross income from Sponsored-Initiated Clinical Trials, Malaysia has become a competitive hub for clinical trials in the world. Alongside this, knowledge propagation brought by Investigator-Initiated Clinical Trials is also paramount. Accordingly, the MedTrial team is committed to providing resources and support to advance the IIR niche in Malaysia.

The MedTrial team is dedicated to supporting the successful execution of Investigator-Initiated Research (IIR) by providing comprehensive assistance and guidance. Our mission is to foster a collaborative environment that empowers researchers to conduct high-quality IIR studies that contribute to the advancement of medical knowledge and patient care. We are committed to ensuring that investigators have the necessary tools, resources, and expertise to navigate the complexities of the research process and achieve their research goals effectively.

Through our specialized knowledge and experience in navigating Malaysian regulations, we provide tailored support to investigators, helping them navigate the regulatory landscape, gain necessary approvals, and ensure ethical conduct throughout the research process. Our mission is to facilitate the seamless execution of IIR studies in Malaysia while upholding the highest standards of integrity, compliance, and patient safety.

Clinical Trial Management Services

What we can do for you

site initiation

Site Initiation

  • Feasibility study

  • Protocol development

  • Clinical trial budget

  • Clinical trial agreement

  • IRB/IEC & regulatory compliance

  • Project management

trial monitoring

Trial Monitoring

  • Site management

  • Product training

  • Clinical trial logistics

  • Safety monitoring



  • Data management

  • Statistical analysis

  • Site closeout logistics

  • Medical writing and publication

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