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GleneaglesCRC provides a full spectrum of front-end and back-end services from Phase I to IV, to handle all of your drug development requirements. We have top-class facilities in every therapeutic area, an extensive hospital network, the shortest approval timelines in the Asia-Pacific Region, and the expertise of over 3,000 specialists across the therapeutic spectrum so that we can ensure that your project succeeds.

  • Pre-Clinical Studies
  • Protocol Development
  • Feasibility Studies
  • Site & Investigator Identification
  • IRB/IEC Submission
  • Regulatory Affairs
  • Clinical Trial Co-Ordination
  • Clinical Trial Monitoring
  • Clinical Trial Project Management
  • Clinical Pharmacokinetics & Pharmacodynamics Studies
  • Laboratory Services
  • Data Management & Biostatistical Analysis
  • Medical Writing
  • Auditing
  • GCP Training
  • Medical and Pharmaceutical Text Translation
  • Pharmacovigilance
  • CRA Outsourcing (China)
  • SMO Services (Singapore)

If you are interested in a cost estimate of our services, you can download a more detailed list of our services on this page; simply tick the services you would like us to perform and fax it to us at (65) 6471 3642.

We look forward to hearing from you!


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