Thanks to CT-SCOUTTM you can identify the studies running at your site that could be worth considering for a patient. No need to know or remember all studies criteria: CT-SCOUTTM powerful algorithm will efficiently support you in identifying the potential appropriate studies. CT-SCOUTTM can also help you coordinate the research activities with your colleagues
Our web and mobile application exclusively designed for investigators, with its easy-to-use questionnaire.
Minimize the administrative burden and redundancy that keeps you and your site staff from focusing on clinical research and patient care.
Help your patients expand access to clinical trials by integrating CT-SCOUT
Receive alerts when a patient is identified and track your patients in a decentralized manner
September 2, 2024
17 September 2024 – 11am – 12:30pm EDT Register for this webinar to receive essential updates on the CDISC transition and learn about new regulations and initiatives impacting Trial Master Files (TMF). Don’t miss this opportunity to stay informed about the latest industry standards and practices. Read more and register: https://cdisc.zoom.us/webinar/register/WN_WqNz9_hiRVihH_pe1IEurA#/registration
September 2, 2024
Med City News Innovation is not just a luxury but a necessity in the realm of clinical trials, particularly as we strive to accelerate drug development. Yet, the slow pace of innovation within the U.S. clinical trials system has impeded progress, leaving many stakeholders frustrated. U.S. Food and Drug Administration (FDA) resource limitations cause the […]
September 2, 2024
International Biopharma Data integrity is critical in Biopharma manufacturing yet is often difficult to achieve due to complex regulatory requirements and legacy data management systems, among the many factors. Furthermore, issues such as data accuracy, completeness and security impact product quality, regulatory compliance and ultimately patient safety. Addressing all these challenges demands a multifaceted approach […]