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: info@convex.bg