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    • Pharmacovigilance
      • PV Outsourcing
      • PV Audit
      • Literature Search
    • Clinical Operations
      • Clinical Studies
      • Protocol Development
      • Site Management
      • Clinical Monitoring
      • PV and ADRs Reporting
      • Quality Assurance
      • Data Management
      • Medical Writing
      • Regulatory Services
    • VIGIPX Safety Database
    • About Us
    • Contact Us
    • Careers
    • Training Courses
      • PV Training
      • CTD Training
Insight

Signed in as:

filler@godaddy.com

  • Home
  • Pharmacovigilance
    • PV Outsourcing
    • PV Audit
    • Literature Search
  • Clinical Operations
    • Clinical Studies
    • Protocol Development
    • Site Management
    • Clinical Monitoring
    • PV and ADRs Reporting
    • Quality Assurance
    • Data Management
    • Medical Writing
    • Regulatory Services
  • VIGIPX Safety Database
  • About Us
  • Contact Us
  • Careers
  • Training Courses
    • PV Training
    • CTD Training

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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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