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