Bioequivalence and bioavailability study SERVICES

 Convex team provides clients with End-to-End Bioavailability & Bioequivalence services for biotech and generic companies.

 

Convex services includes:     Convex expertize includes:
     
  • Study protocol development
                  
  • Single and multiple dose design
  • Medical writing
 
  • Parallel design
  • QP release
 
  • Crossover design (Two-way, Three-way, Four-way)
  • Secondaty lablelling and packaging
 
  • Fasting or fed state
  • CTA document preparation
   
  • Study submission to RA/EC
   
  • Regulatory consultation
   
  • Contracting
   
  • Investigator meeting set-up
   
  • Healthy subject recruitment
   
  • Clinical operations and studyconduct
   
  • Project management
   
  • Clinical monitoring
   
  • Safety reporting
   
  • Bioanalytical analysis
   
  • Data management
   
  • Electronic data capture (e-CRF)
   
  • Biostatistics
   
  • Final study report development
   

  

For more information, please contatc us at: info@convex.bg