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Clinical Studies

  • Phase I, II, III, IV clinical trials and evidence in real-life medical practice.
        • Project management.
        • Site selection.
        • Feasibilities.
        • Investigators´ meetings.
        • Training for site personnel.
        • Study start-up.
        • Monitoring onsite, remote and on demand).
        • Medical data review.
        • Risk evaluation.
        • TMF (Study Master File)
 
  • Local trials (observational and epidemiological).
  • Expanded access and compassionate use.
  • Management of clinical supplies and local vendors.
  • Spanish /English translation
  • Negotiation and budget management.

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