Clinical Trial Services
IATEC Clinical Trial Services is an independent, full-service Contract Research Organization (CRO) that offers a comprehensive package of research services for the pharmaceutical industry. Working closely with our clients, we are committed to providing customized services that meet the required standards of quality - on time and within budget.

IATEC uses state-of-the art tools for data management, database construction and SAS® for data validation and descriptive and inferential statistics. Each of our individual activities, from protocol(Studieprotocol) Document waarin wordt beschreven waarom een studie gedaan wordt en hoe deze precies zal worden uitgevoerd. development and writing, validation and production, to data management, statistical analyses and report writing, is carefully monitored to ensure that we are always able to provide good-quality services.

IATEC offers a set of tailor-made services that meet the international quality standards of regulatory bodies such as the ICH, CPMP and FDAFood and Drug Administration: het regulerende orgaan dat toeziet op de
ontwikkeling en goedkeuring van geneesmiddelen in de Verenigde Staten.. Our own system of quality control ensures that our standards are guaranteed at all levels.

If you have any questions about this or other information, or would like to get in touch with IATEC, please contact Remko van Leeuwen or Julian Suurmeijer, Directors Business Development, at +31 20 3149300.