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    • Home
    • Pharmacovigilance
      • PV Outsourcing
      • PV Audit
      • Literature Search
    • CRO Services
      • Project Management
      • Protocol Development
      • Site Management
      • Clinical Monitoring
      • PV and ADRs Reporting
      • Quality Assurance
      • Data Management
      • Medical Writing
      • Regulatory Services
    • Safety Database
      • Vigipx
    • Training Courses
      • PV Training
      • CTD Training
      • Open Registration
    • Careers
    • About Us
    • Contact Us
Insight
  • Home
  • Pharmacovigilance
    • PV Outsourcing
    • PV Audit
    • Literature Search
  • CRO Services
    • Project Management
    • Protocol Development
    • Site Management
    • Clinical Monitoring
    • PV and ADRs Reporting
    • Quality Assurance
    • Data Management
    • Medical Writing
    • Regulatory Services
  • Safety Database
    • Vigipx
  • Training Courses
    • PV Training
    • CTD Training
    • Open Registration
  • Careers
  • About Us
  • Contact Us

Clinical Monitoring

Our clinical operations team oversees every aspect of the clinical trial process, from protocol development to data management, to ensure that trials are conducted according to regulatory standards and best practices. 


Our team conducts regular monitoring visits to ensure participant safety, data integrity, and regulatory compliance at investigative sites, this includes source data verification, review of study documentation, assessment of protocol adherence, and safety reporting.

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