Welcome to Crossover
Crossover collaborates with a network of healthcare institutions to identify and recruit patients into clinical trials via dedicated clinical research units which it establishes, staffs and manages.
Crossover CRI AG (Crossover) runs a network of Clinical Research Units (CRUs) in partnership with research-driven healthcare institutions. Our CRUs are located on-site at the healthcare institutions and have professional and dedicated Crossover staff managing the entire portfolio of clinical trials at the institutions they serve. The key roles of the CRUs are to train research teams within the healthcare institutions on good clinical practice (GCP), regulatory guidelines and protocol-specific needs, to enable them to manage the projects, support investigative teams and conduct in-process quality control. Crossover provides on-site administrative resources for the investigators and also manages the clinical trial dataflow, either paper-based or electronic.
News
The Board of Directors of the European Forum for GCP confirmed Jean-Pierre Tassignon as Chairman of the Board for another year. Jean-Pierre has chaired the EFGCP Board since 2005 - www.efgcp.be.
Events
EFGCP Annual Conference, Prague: Stuart Cummings, Vice President Clinical Research and Hospital Information Systems at Crossover, will be the Rapporteur of a workgroup discussing how biostatisticians can contribute to the detection of fraud in clinical research. The conference is dedicated to the “Integrity of Biomedical research within Europe”.