Literature DB >> 30734900

GDPR: an impediment to research?

Niamh Clarke1,2, Gillian Vale1, Emer P Reeves3,4, Mary Kirwan1,2, David Smith1,2, Michael Farrell1, Gerard Hurl5, Noel G McElvaney1,2,5.   

Abstract

BACKGROUND: The recent introduction of the General Data Protection Regulation and Health Research Regulations has been an area of significant concern for those engaged in clinical research. These European regulations, following subsequent interpretation by Ireland's Department of Health, now place Ireland in a unique position which differs substantially from other European countries and may prove a significant impediment to Irish clinical research, depriving Irish patients of timely access to potentially life-saving treatments and making Ireland less attractive to pharmaceutical companies engaged in this area. At the very least, the regulations, as applied in Ireland, will place a significant extra burden of work on Ireland's clinical researchers and at their worst will force individuals and institutions out of the clinical research field, which will result in significant loss to the Irish knowledge economy and lead to the detriment of patient care. AIM: In this article, we explore what exactly is proposed by Europe's GDPR and by Ireland's Health Research Regulations. We look at the challenges presented to clinical researchers, and we highlight those areas, which need clarification by the Department of Health and by the Data Protection Commissioner.
CONCLUSIONS: We propose five recommendations, which would ameliorate some of the more restrictive impositions of these regulations. This review was commissioned by the Irish Academy of Medical Science.

Entities:  

Keywords:  Biobanks/archival material; Capacity to consent; General Data Protection Regulation; Health Research Regulations; Retrospective chart reviews

Mesh:

Year:  2019        PMID: 30734900     DOI: 10.1007/s11845-019-01980-2

Source DB:  PubMed          Journal:  Ir J Med Sci        ISSN: 0021-1265            Impact factor:   1.568


  2 in total

1.  Consent for continuing research participation: what is it and when should it be obtained?

Authors:  Dave Wendler; Jonathan Rackoff
Journal:  IRB       Date:  2002 May-Jun

2.  When should re-consent of subjects participating in a clinical trial be requested? A case-oriented algorithm to assist in the decision-making process.

Authors:  R Dal-Ré; C Avendaño; A Gil-Aguado; D Gracia; A L Caplan
Journal:  Clin Pharmacol Ther       Date:  2007-09-19       Impact factor: 6.875

  2 in total
  8 in total

1.  What GDPR and the Health Research Regulations (HRRs) mean for Ireland: "explicit consent"-a legal analysis.

Authors:  Mary Kirwan; Blanaid Mee; Niamh Clarke; Aoife Tanaka; Lino Manaloto; Emma Halpin; Una Gibbons; Ann Cullen; Sarah McGarrigle; Elisabeth M Connolly; Kathleen Bennett; Eoin Gaffney; Ciaran Flanagan; Laura Tier; Richard Flavin; Noel G McElvaney
Journal:  Ir J Med Sci       Date:  2020-07-30       Impact factor: 1.568

2.  Readability and understandability of clinical research patient information leaflets and consent forms in Ireland and the UK: a retrospective quantitative analysis.

Authors:  Lydia O'Sullivan; Prasanth Sukumar; Rachel Crowley; Eilish McAuliffe; Peter Doran
Journal:  BMJ Open       Date:  2020-09-03       Impact factor: 2.692

3.  What GDPR and the Health Research Regulations (HRRs) mean for Ireland: a research perspective.

Authors:  Blanaid Mee; Mary Kirwan; Niamh Clarke; Aoife Tanaka; Lino Manaloto; Emma Halpin; Una Gibbons; Ann Cullen; Sarah McGarrigle; Elisabeth M Connolly; Kathleen Bennett; Eoin Gaffney; Ciaran Flanagan; Laura Tier; Richard Flavin; Noel G McElvaney
Journal:  Ir J Med Sci       Date:  2020-07-29       Impact factor: 1.568

4.  Using linked administrative health data for palliative and end of life care research in Ireland: potential and challenges.

Authors:  Maria Kelly; Katie O'Brien; Ailish Hannigan
Journal:  HRB Open Res       Date:  2021-02-09

5.  "Data is the new oil": citizen science and informed consent in an era of researchers handling of an economically valuable resource.

Authors:  Etain Quigley; Ingrid Holme; David M Doyle; Aileen K Ho; Eamonn Ambrose; Katie Kirkwood; Gerardine Doyle
Journal:  Life Sci Soc Policy       Date:  2021-12-10

6.  Enablers and barriers to the secondary use of health data in Europe: general data protection regulation perspective.

Authors:  Jakov Vukovic; Damir Ivankovic; Claudia Habl; Jelena Dimnjakovic
Journal:  Arch Public Health       Date:  2022-04-09

7.  A short report of Biosafety and Biobanking: current understanding and knowledge gaps.

Authors:  Julie Roux; Maissa Zeghidi; Stephanie Villar; Zisis Kozlakidis
Journal:  Biosaf Health       Date:  2021-06-19

Review 8.  Challenges of international oncology trial collaboration-a call to action.

Authors:  Monica Tang; Heikki Joensuu; Robert J Simes; Timothy J Price; Sonia Yip; Wendy Hague; Katrin M Sjoquist; John Zalcberg
Journal:  Br J Cancer       Date:  2019-08-05       Impact factor: 7.640

  8 in total

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