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: