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Clinical -Trial Consultancy Services

Trial Consultancy Services

  1. Site Identification and feasibility
  2. Monitoring and Site closeout
  3. EC submissions and communications
  4. Site Management and Project management
  5. Clinical Operations Support /GCP documents / Ensuring Study compliance
  6. Data Entry, Data Management and query resolutions support to CRO/Sponsor
  7. Recruitment of CRC and Study Nurse and other supporting staff for CRO/Sponsor Clinical Trials.

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