CRU-RISE offers expertise and support for the design, implementation, and management of clinical research studies, as part of the Portuguese Clinical Research Infrastructure Network (PtCRIN) and as a partner of European Clinical Research Infrastructure Network (eCRIN). With a multidisciplinary approach and compliance with international standards, including ICH-GCP guidelines, CRU-RISE ensures the delivery of high-quality and efficient research solutions tailored to investigator-driven and academic-led studies.

As an ECRIN partner, CRU-RISE provides the necessary logistical support to perform multinational clinical research in Europe, with special emphasis on Investigator-Initiated Studies.
CRU-RISE is a structure to support Investigator-Initiated and Industry-Sponsored Clinical Research complying with ICH GCP – Good Clinical Practice Guidelines and European regulations, namely Clinical Trials Regulation (Regulation (EU) No 536/2014), Medical Devices Regulation (Regulation (EU) No 2017/745) and General Data Protection Regulation (EU) 2016/679. We provide pharmacovigilance services that comply with the GVP – Good Pharmacovigilance Practices and ISO 14155 – Clinical Investigation of Medical Devices for Human Subjects.