Assessment and sites selection in Bulgaria
feasibility and site selection
Negotiating study contracts and budgets is critical point for the
Clinical study protocols, ICFs, study final report
Clinical trials application, Scientific advise, CT Amendments
Convex clinical monitoring team CRAs are experts in the performance of all clinical monitoring activities and provide full range of CRO activities including : SDV of source documentation, ICF, patient eligibility, study protocol procedures compliance and etc. Our CRAs have all required education and trainings and can support any clinical study design. We work in Bulgaria Western Europe.
We provide full transparency and constant point of contact.
biostatistics and data management
Our Biostatistical and Data management services include:
For the bioanalytical part of a study our preferred partner is