Crossover Clinical Research Infrastructures Network (COCRIN)
Crossover is building a network of Clinical Research Units (CRUs) at a number of healthcare institutions with which it will have Master Clinical Research Cooperation Agreements.

Each of these agreements ensures

  • All clinical research at the healthcare institution will be managed through the Crossover CRU
  • A common approach to clinical research standards is adopted and followed at each Crossover CRU
  • Each healthcare institution allows access to the healthcare information system (HIS)
  • Data from the various institutions' patients can be merged (after de-identification) into Crossover’s epidemiological database (EPIDAB)

This rich network of CRUs provides sponsors with immediate access to a raft of highly specialised clinical researchers, adhering to a common set of standard operating procedures and fully trained and compliant in the principles of good clinical practice (GCP). Moreover, access to the network permits sponsors to reduce the time it takes to establish the feasibility of a protocol, the setting up of a multi-centre study and the recruitment of patients. Because close attention is paid to the recruitment of suitable patients who are supported throughout the clinical trial by Crossover CRU staff, the attrition rate is reduced and the time to last patient last visit (LPLV) is also thereby reduced.

The following are the COCRIN membership options for your Healthcare Institution:
  • You become a COCRIN Partner, maintain your own existing institutional CRU, and receive the Crossover SOPs, training and annual audits. Crossover markets COCRIN worldwide to sponsors and brings clinical trials to its Partners;
  • You become a COCRIN Supported Partner by establishing your own institutional CRU, and receiving all of the above, plus initial and ongoing management support;
  • You become a COCRIN Co-Development Partner by establishing a Crossover CRU, and receiving all of the above, plus Crossover will equip and staff the CRU – including CRF data entry – at its cost, where you provide the space;
  • You become a COCRIN Full-Development Partner by establishing a Crossover CRU, and receiving all of the above, plus Crossover will provide the office for the CRU on your campus;
  • If your Institution already has an institutional CRU, you may want to discuss a transfer to Crossover.

If your Healthcare Institution is interested in one of the COCRIN partnering options, please click on Registration in the left menu and fill out the questionnaire.

  • HUDERF and its Crossover
    Clinical Research Unit join
    the Belgian Pediatric
    Clinical Research ... more
  • The Hôpital
    Universitaire des Enfants
    Reine Fabiola (HUDERF)
    joins COCRINCrossover ... more
  • The GCP Journal 2008 Award
    Ceremony will take place
    this year on the 22nd of
    October again in London. ... more
  • BPCM academic meeting on 16
    January 2009 in Brussels.
    Jean-Pierre Tassignon, who
    is a Fellow of the Belgian ... more
  • ECRIN Network Development
    Board meeting on 7 January,
    2009 in Brussels.
    Jean-Pierre Tassignon, who ... more
  • Crossover Participates in
    European Conference on
    Research Misconduct
     The European Forum ... more