SAHCRO study managers provide outstanding leadership for your studies. Their broad-based veterinary medicine expertise provides scientific credibility to your trial. Their depth of expertise in clinical trials allows your trial to move forward smoothly and within the timelines. All trials are conducted under Veterinary ICH Good Clinical Practices.

Sahcro Trial Managers Provide the Following Services:

Study Management

  • Clinical Trial Design
  • Protocol Development
  • Organization and Archiving of Regulatory Documentation and Trial
  • Master File
  • Investigator Meetings
  • Site Staff Training
  • Drug/Device Accountability
  • Vendor Management

Site Management

  • Source Document Development
  • Study Monitoring
  • Write Study Monitoring Plans
  • Site Qualification, Site Initiation, Interim and Close-Out
  • Monitoring Visits
  • Study Monitoring Reports

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