Literature DB >> 15745195

Over-regulation of clinical research: a threat to public health.

Charles Warlow1.   

Abstract

Clinical research is subject to increasing regulation by research ethics committees and research and development offices which are responding to social and political pressures, as well as to new legislation, both European and national, some of which is still being worked out. The resulting bureaucracy, expense and confusion are putting insuperable hurdles in the way of clinical research and clinical care is compromised. What research is still possible will only be done in large organisations and may even be seriously biased. The solutions are to inform and seek the help of the public and to forge alliances with patient groups. Patients have far more to lose than clinical researchers who, if clinically qualified, can more easily pursue a fulfilling career as clinicians rather than researchers.

Entities:  

Keywords:  Biomedical and Behavioral Research; Data Protection Act 1998 (Great Britain); Legal Approach

Mesh:

Year:  2005        PMID: 15745195      PMCID: PMC4954064          DOI: 10.7861/clinmedicine.5-1-33

Source DB:  PubMed          Journal:  Clin Med (Lond)        ISSN: 1470-2118            Impact factor:   2.659


  7 in total

1.  Could parenting programs lead to lower health care costs in future generations?

Authors:  Sarah Stewart-Brown
Journal:  CMAJ       Date:  2011-11-14       Impact factor: 8.262

2.  Using personal health information in medical research.

Authors:  Tom Walley
Journal:  BMJ       Date:  2006-01-21

3.  Increasing value and reducing waste in biomedical research regulation and management.

Authors:  Rustam Al-Shahi Salman; Elaine Beller; Jonathan Kagan; Elina Hemminki; Robert S Phillips; Julian Savulescu; Malcolm Macleod; Janet Wisely; Iain Chalmers
Journal:  Lancet       Date:  2014-01-08       Impact factor: 79.321

4.  Bureaucracy stifles medical research in Britain: a tale of three trials.

Authors:  Helen Snooks; Hayley Hutchings; Anne Seagrove; Sarah Stewart-Brown; John Williams; Ian Russell
Journal:  BMC Med Res Methodol       Date:  2012-08-16       Impact factor: 4.615

5.  The role of the user within the medical device design and development process: medical device manufacturers' perspectives.

Authors:  Arthur G Money; Julie Barnett; Jasna Kuljis; Michael P Craven; Jennifer L Martin; Terry Young
Journal:  BMC Med Inform Decis Mak       Date:  2011-02-28       Impact factor: 2.796

Review 6.  Research governance: where did it come from, what does it mean?

Authors:  Sara Shaw; Petra M Boynton; Trisha Greenhalgh
Journal:  J R Soc Med       Date:  2005-11       Impact factor: 18.000

7.  Varying ethics rules in clinical research and routine patient care--research ethics committee chairpersons' views in Finland.

Authors:  Elina Hemminki; Jorma I Virtanen; Piret Veerus
Journal:  Health Res Policy Syst       Date:  2014-03-25
  7 in total

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