Clinical Trials



Medical Writing & Submission

Clinical Trials

  • Clinical Study Design and Protocol Development
    • Study design for clinical trials, clinical
      outcome studies, therapeutic equivalence studies
    • Protocol development
    • Statistical planning and sample size estimation
    • Literature review and meta analysis
    • Case Report Form development
  • Clinical Trial Management
    • Site Initiation
      • Site and investigator selection
      • Site initiation
      • Site personnel training
    • Site monitoring
      • Source data verification
      • Monitoring of patient eligibility and enrolment into trial
    • Project Management
      • Clinical Research Associate services
      • Study coordination with study sites, sponsor and study related vendors
      • Management of deliverables and progress reports
      • Serious Adverse Events reporting
  • Clinical Database Design
    • Design of data entry and database applications
    • Data security management and procedures
  • Clinical Data Management
    • Design of the data management plan based on project
      data management requirements and SOPs
    • Case Report Form data entry
    • Evaluation of clinical data consistency
    • Site data query
    • Case Report Form retrieval and management
    • Document archiving


Latest News

17/04/2018 - 19/04/2018
DIA 30th Annual Euromeeting

07/05/2018 - 09/05/2018
7th Annual Clinical Trial Innovation Summit

24/06/2018 - 28/06/2018
DIA 2018 Global Annual Meeting

19/10/2018 - 23/10/2018
ESMO 2018 Congress

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