Requirements for Certification of ECRIN Data Centres, with Explanation and Elaboration of Standards, Version 3.0
- 1. Independent consultant
- 2. Mario Negri Institute, Milano
- 3. Centre d'Investigation Clinique, Hospices Civils de Lyon, Lyon
- 4. Leeds Institute of Clinical Trials Research
- 5. Clinical and Epidemiological Investigation Center, Luxembourg Institute of Health
- 6. Data Centre, Coimbra Coordinating Centre for Clinical Research, AIBILI, Coimbra
- 7. National University of Ireland, Galway
- 8. Clinical Pharmacology and Clinical Trials Department, University Hospitals, Faculté Laennec, Lyon
- 9. Dept. of Biostatistics, Odense University, Odense
- 10. European Clinical Research Infrastructures Network (ECRIN), Prinz-Georg-Str. 51, 40477 Düsseldorf
- 11. Institut de Santé Publique, d'Epidémiologie et de Développement, Bordeaux
- 12. Life and Health Sciences Research Institute (ICVS), School of Health Sciences, University of Minho, Braga; ICVS-3Bs PT Government Associate Laboratory, Braga, Guimarães
- 13. PCG Clinical Services AB, Uppsala
- 14. Inter-disciplinary Centre for Clinical Trials (IZKS) Mainz
- 15. Centre for Clinical Trials, Philipps-University Marburg
This document represents version 3 of the ‘Requirements for certification of data centres’, published by ECRIN, the European Clinical Research Infrastructure Network (the first version was produced in 2011, and the second in 2012). The requirements are the criteria used by ECRIN to identify, and then certify, clinical trials units that can provide high quality, compliant and safe data management, as well as effective management of the underlying systems and IT infrastructure. This latest version results from a review in 2015 by ECRIN auditors, members of ECRIN’s data centre Certification Board, and invited experts from a variety of trials units in Europe, and it reflects experience gained auditing trials units in 2014.
Over and above their use for certification, the requirements are intended to describe good practice in data and IT management in clinical research, and in clinical trials in particular. They were developed by senior staff working in non-commercial clinical trials units in Europe, and are intended as a practical guide for staff working in IT and data management in that sector (though the same principles apply to all clinical research environments).
The 129 requirements, or standards, included in the current version are divided into 19 separate lists, some focused on IT, some mainly concerned with data management, and some that deal with both. Each standard has a code, a title, and a single statement summarizing the requirement. This document provides, in addition, explanatory and elaboration material – usually a few paragraphs that attempt to clarify each statement’s meaning, and / or give examples of its application, and which also indicate the evidence that would normally be used to assess a unit’s compliance. The document also includes a brief introduction to the standards and their development, including a description of the ECRIN audit process, and a glossary of terms.
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