Icta Pm

ICTA is an international privately-owned CRO with 40 years of experience in clinical R&D, pharmaco-epidemiology and Early and Compassionate programs for traditional and advanced therapies (including biologics cell and gene products), diagnostics and medical devices with over Clinical Projects. ICTA’s international operations in Western/Eastern Europe and North America provide full clinical research or “a la carte” services in traditional and adaptive clinical trials from Early Phase to Late Phase across a broad range of therapeutic areas. Additionally, ICTA’s consulting unit provides the pharmaceutical, medical device and biotech industries with strategic advice at every stage of your clinical developments. Our full-services offering : from drafting essential study documents to overseeing extensive medical writing programs : helping you anticipate challenges, overcome obstacles, and chart a clear, compliant path forward : we ensure seamless execution across every phase of your clinical study : Our Clinical Research Assistants offer you their knowledge of local investigational structures to give you cost effective solutions : improve data quality, ensure study continuity and reduce site burden: a wide range of safety services for your clinical research projects : from CRF design to final database lock, adapted to the context of each study : ICTA biometry services to generate high-quality and reliable data for informed decision making: Medical Writing: flexible medical writing solutions to support your clinical program needs Contact us by using the form on our website