Study Coordination


To assure the conduction of the study according to high quality standards in the clinical research centers (healthcare units):

  • Regulatory support to get the local site approval
  • Support the Research Team across clinical trial procedures
  • Study coordination in the site
  • Sample management, with storage requirements
  • Trial materials development & guidance notes for investigator & pharmacy files
  • Monitoring patient reimbursements and research teams payments
  • Identify & address barriers to timely recruitment and conduct
  • Facilitation of audits & regulatory inspections in the local site
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