Member of a EUCROF member association

Design and management of early and late phase clinical studies, Non Interventional Studies and RWE studies, Early Access and Compassionate Programs

100-200

Call Center,Clinical Monitoring,Clinical Trial Supply Services,Data Management,eCRF & other eTools,Investigator Network,IVRS/IWRS,Medical Advising,Medical Writing,Patient recruitment,Pharmacovigilance,Project Management,Regulatory Affairs,Statistics

Ph I clinical trials,Ph II clinical trials,Ph III clinical trials,Ph IV /NIS,Registries

Oncology,Haematology,Cardiovascular Diseases,Metabolic Diseases,Central Nervous System (CNS) Disorders,Respiratory,Diabetes / Endocrinology,Infectious Diseases,Ophthalmology,Rheumatology,Immunology,Rare Diseases,Paediatrics,Women’s health

Drug,Medical Device,Diagnostics,ATMP,Biosimilar /Bioequivalent

Belgium,Bosnia and Herzegovina,Bulgaria,Canada,Croatia,Czech Republic,Denmark,Estonia,Finland,France,Germany,Greece,Guadeloupe,Hungary,Italy,Latvia,Lithuania,Martinique,Netherlands,Norway,Poland,Portugal,Romania,Russia,Slovakia,Slovenia,Spain,Sweden,Switzerland,Ukraine,United Kingdom,United States

ISO 9001:2015 certified in French and international project management - ISO 27001:2013 in information security in clinical research and health programs

ICTA offers a range of secure, configurable and easy-to-use solutions enabling the full or partial decentralisation of clinical studies in compliance with regulations in force