CRCs are health care-based organizations with infrastructures prepared to develop clinical trials such as: hospitalization beds, medical equipment, specialized health care professionals including medical and study-nurse staff,repliche rolex allowing the enrolment of patients in the early phases of drug trials and also in non-therapeutic studies.
It is our goal to contribute to the establishment of high quality clinical research centers in Portugal, recognized by all national and international partners in this field.

Academic CTUs/CROs that manage clinical trials and other interventional studies, namely randomised clinical trials, prognostic studies, diagnostic studies, and meta-analyses. They also deal with the design, organization, logistics of the study, participate in center selection, data management, monitoring, data analysis, pharmacovigilance and reporting.
Academic CTUs/CROs bring together experts needed to conduct a clinical trial, including physicians, statisticians and study managers. They operate as the interface between all the stakeholders in clinical trials.
Academic CTUs/CROs can provide either general or particular services in areas such as (e.g. oncology, ophthalmology, etc.) or even provide specific assistance (e.g. statistics, protocol design, monitoring, fake louis vuitton bag pharmacovigilance, data management, etc.).

Organizations capable of acting both as CRCs and Academic CTUs/CROs.
Their objective is to provide services in academic clinical research and advise on legal requirements and ethical concerns.