Phase I Clinical Research Unit

bioequivalence bioavailability study in eastern europe bulgaria

bioequivalence bioavailability study in eastern europe bulgaria

Convex team has extensive experience in the conduct of bioequivalence and bioavailability study in Eastern Europe, Bulgaria. We are experts in the clinical operation and management of Crossover and Parallel Design, Single Dose and Multi Dose, Healthy Subject and Patient Population, Administered Dose, Sampling, Parent Drug and Metabolites, Enantiomers and Racemates, Endogenous Compounds, Food-Effect BA study, Fast Fed BE study, Drug-drug interaction studies. State of the art clinical research facility and early phase clinical research team has the required expertise to conduct clinical trials on healthy volunteers and patient population on BE and BA studies. On the other hand, our CRO department will make sure to conduct all contract research activities on behalf of sponsored single center clinical studies

CLINICAL STUDIES IN PHASE I in Eastern Europe Bulgaria

CLINICAL STUDIES IN PHASE I in Eastern Europe Bulgaria

Convex early phase clinical research team focus on Phase I clinical trials. Our research center with a built-in phase I unit in which we have the capabilies and expertize to conduct clinical trials in early phase included First in Man and Phase I clinical studies. Our Phase I Unit is located in Bulgaria, Easter Europe and has the capability to enroll study subjects for shorten period of time as supported by our recruitment specialists. Our phase I team includes principal investigators specialized in Cardiology Pulmonology Dermatology Endocrinology Neurology Gastroenterology and Rheumatology. Convex Center for early phase human research is located in Sofia, Bulgaria Eastern Europe and has great access to large patient population and healthy volunteers. We maintain a database of healthy subject and provide shorter timelines for recruitment.

CLINICAL STUDIES IN PHASE II - IV in Eastern Europe, Bulgaria

CLINICAL STUDIES IN PHASE II - IV in Eastern Europe, Bulgaria

Convex late phase clinical research teams are focused on the conduct of clinical trials in phase II to phase IV. Our team expertise includes hundreds of clinical studies conducted within the past 20 years. We have been inspected and audited by RA and sponsors companies. Our teams included principal investigators, sub-investigators, clinical studies coordinators, recruitment specialist, study nurses, study technicians, project managers, clinical trial director. We collaborate with Sponsors and Global CROs planning to conduct their clinical trials either single center or multicenter trials in Bulgaria, Eastern Europe.

CLINICAL STUDIES ON FOOD SUPPLEMENTS IN EASTERN EUROPE BULGARIA

CLINICAL STUDIES ON FOOD SUPPLEMENTS IN EASTERN EUROPE BULGARIA

In spite of the simpler regulatory procedure, we take the clinical conduct of a food supplement study with the same level of responsibility as any other study. We conduct clinical studies on vitamins, dietary supplement and food. As single-center experts we have few advantages, shorten approval process, fast study subjects recruitment process, clinical operations. We are fully transparent and dedicated to your project. Bulgaria is one of the most common destination for the conduct of clinical trials on dietary supplement and vitamins.

Pilot pivotal ON MEDICAL DEVICES in Eastern Europe Bulgaria

Pilot pivotal ON MEDICAL DEVICES in Eastern Europe Bulgaria

Convex CRO and Center for clinical investigations on medical devices supports single center studies on medical devices involving patient population and healthy volunteers. We manage and conduct medical device clinical trials in variety of therapeutic areas. We are located in Sofia, Bulgaria, Eastern Europe which allows us to have database of potential subject for your study.

CRO Services in Eastern Europe Bulgaria

CRO Services in Eastern Europe Bulgaria

We provide all services required and cover the entire drug development process included start up activities, medical writing, regulatory services, contracting, clinical operations, study subjects recruitment and retention, clinical monitoring, project management, labeling and packaging, data management and biostatistics writing of clinical study report