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 1,000 Clinical Projects.

ICTA’s international operations in Western/Eastern Europe and North America provide full clinical research or “à 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 :

- 𝗗𝗲𝘀𝗶𝗴𝗻: from drafting essential study documents to overseeing extensive medical writing programs

- 𝗥𝗲𝗴𝘂𝗹𝗮𝘁𝗼𝗿𝘆 𝗮𝗳𝗳𝗮𝗶𝗿𝘀: helping you anticipate challenges, overcome obstacles, and chart a clear, compliant path forward

- 𝗣𝗿𝗼𝗷𝗲𝗰𝘁 𝗺𝗮𝗻𝗮𝗴𝗲𝗺𝗲𝗻𝘁: we ensure seamless execution across every phase of your clinical study

- 𝗦𝗶𝘁𝗲 𝗦𝘂𝗽𝗽𝗼𝗿𝘁: our Clinical Research Assistants offer you their knowledge of local investigational structures to give you cost effective solutions

- 𝗥𝗶𝘀𝗸-𝗯𝗮𝘀𝗲𝗱 𝗺𝗼𝗻𝗶𝘁𝗼𝗿𝗶𝗻𝗴: improve data quality, ensure study continuity and reduce site burden

- 𝗣𝗵𝗮𝗿𝗺𝗮𝗰𝗼 𝗮𝗻𝗱 𝗺𝗮𝘁𝗲𝗿𝗶𝗼𝘃𝗶𝗴𝗶𝗹𝗮𝗻𝗰𝗲: a wide range of safety services for your clinical research projects

- 𝗗𝗮𝘁𝗮 𝗺𝗮𝗻𝗮𝗴𝗲𝗺𝗲𝗻𝘁: from CRF design to final database lock, adapted to the context of each study

- 𝗕𝗶𝗼𝘀𝘁𝗮𝘁𝗶𝘀𝘁𝗶𝗰𝘀: 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