About us
The Crossover clinical research model
Crossover CRI AG (Crossover) is currently establishing a large international network of Clinical Research Units (CRUs) in research-driven healthcare institutions. Our CRUs are located on-site at the healthcare institution to enable the collection and analysis of healthcare information both in clinical trials and epidemiology studies.

Crossover invests in establishing and staffing the CRUs that are responsible for conducting all clinical trials carried out at the selected healthcare institutions which are part of the Crossover network. Over the next 10 years, it is expected that this network will expand to include more than 175 healthcare institutions in all parts of the world.

In parallel, Crossover establishes access to the hospital information systems (HIS) of healthcare institutions within the network, populating on a continuous basis the Epidemiology Database (EPIDAB) and warehousing de-identified electronic medical record/electronic health record patient data.

Crossover improves the feasibility of clinical trials and provides population studies of better quality and at a more affordable cost than healthcare institutions without a dedicated CRU. Its epidemiology database (EPIDAB) is used for data mining to support a wide range of medical, scientific and market research needs (interventional and non-interventional clinical trials, non-applied clinical research and market research) of significant interest to pharmaceutical companies, academic researchers, CROs and healthcare planners, providers and insurers.

Crossover offers a new and unique model for clinical research and epidemiology. The advantages over previous models are:
  • Lower costs through proximity with medical technology clusters and the use of academic and healthcare institution staff peripherally on an ad hoc basis rather than central staff
  • Closer cooperation with sponsors through the distribution of project managers at healthcare institutions in close vicinity of sponsor clusters
  • Bridging the gap between healthcare databases and clinical trial databases through the standardisation of work practice and use of internationally recognised coding systems and nomenclature, the continuous development of sophisticated data collection and validation systems in healthcare practice and clinical research, intensive training of staff at research sites and the use of advanced integrated IT systems
  • Objective feasibility studies, faster project turnaround and higher quality
  • Crossover has developed a
    clinical trials database
    for its partner hospitals
    and investigators ... more
  • Nathalie Vandenhoudt, PhD,
    Clinical Study Coordinator
    at the Crossover Clinical
    Research Unit in Brussels ... more
  • Crossover observes a
    continuing decline in
    industry-sponsored clinical
    trials.   Since ... more
  • Lecture at the University
    of Neufchâtel,
    Switzerland  
    Jean-Pierre Tassignon, MD, ... more
  • Public lecture at CHU
    Brugmann, Brussels 
    Prof. Anne Peretz (chair of
    the Clinical Research ... more
  • EFGCP Annual Conference
    2011, Budapest  
    The European Forum for GCP
    organizes the EFGCP Annual ... more