Bioequivalence and bioavailability study SERVICES

Convex Ltd. provides clients with End-to-End Bioavailability & Bioequivalence services for generics companies. Our services include study design, conduct, bioanalysis, data standardization and analysis, dossier preparation and regulatory submissions, and pharmacovigilance.

We have experience in a wide variety of studies including multiple doses, dosage form, dose escalation, single and double blind, PK/PD end point studies, Glucose clamp studies, proof of concept and exploratory, repeat “first in man”, nutritional, special population, drug interaction, and etc.




Convex Ltd. services includes:

  • Protocol Development
  • Medical writing
  • QP release
  • Secondary lablelling anf packaging
  • CTA documents preparation
  • Contracting
  • Regulatory services
  • investigator meeting organization
  • Subject recruitment
  • Clinical operations
  • Clinical monitoring
  • Pharmacovigilance
  • Bioanalytical analysis
  • Data Management
  • Electronic data capturing
  • Biostatistics
  • Final Report


For more information, please contatc us at: