Article info
PDFBrief report
Patient organisations should also establish databanks on medical complications
Citation
Patient organisations should also establish databanks on medical complications
Publication history
- First published April 1, 2003.
Online issue publication
April 01, 2003
Request permissions
If you wish to reuse any or all of this article please use the link below which will take you to the Copyright Clearance Center’s RightsLink service. You will be able to get a quick price and instant permission to reuse the content in many different ways.
Copyright information
Copyright 2003 by the Journal of Medical Ethics
Other content recommended for you
- Financial interests of patient organisations contributing to technology assessment at England’s National Institute for Health and Care Excellence: policy review
- Exposing drug industry funding of UK patient organisations
- Cancer patients’ organisation participation in heath policy decision-making: a snapshot/cluster analysis of the EU-28 countries
- Is the international regulation of medical complicity with torture largely window dressing? The case of Israel and the lessons of a 12-year medical ethical appeal
- Patient–physician collaboration in rheumatology: a necessity
- 2021 EULAR recommendations for the implementation of self-management strategies in patients with inflammatory arthritis
- Access to investigational medicinal products for minors in Europe: ethical and regulatory issues in negotiating children's access to investigational medicines
- Medical complications and deaths in 21 and 56 km road race runners: a 4-year prospective study in 65 865 runners—SAFER study I
- The European Statements of Hospital Pharmacy: the patient and healthcare perspective
- Patient and caregiver priorities in the transition from hospital to home: results from province-wide group concept mapping