Phase IV Studies

YOU ARE

A company active in Pharma, Biotech, or Medtech, a health league, a hospital or a private clinic willing to:

  • Prove the reliability and cost-eff ectiveness of your product versus gold standard methods
  • Evaluate the usability and applicability of a new technology

…for prevention, diagnosis, treatment & patient follow-up at the hospital or at home.


WE OFFER YOU

 

Consulting services

  • Market characterization
  • Medical need & feasibility surveys
  • Literature review
  • Study design
  • KOLs & investigational site identification
  • Procedures for clinical trial authorisation

Medical writing services

  • Survey and analysis reports
  • Documentation for submission to the Ethics Committee
  • Scientific reports and publications

                  

KOLs & STUDY SITE IDENTIFICATION
STUDY DESIGN
PROCEDURES FOR STUDY AUTHORISATION
DOCUMENTATION FOR ETHICS COMMITTEE

OUR APPROACH

You can outsource individual tasks or the overall study design to us. Vivactis helps you plan your study from the design to the reporting phase, in order to be compliant with regulatory and ethical requirements.

For other studies for regulatory perspectives, CE marking submission, or medico-economic analyses for reimbursement strategies, we collaborate with experts from the field, either within the Vivactis Group or outsourced.

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