Improving health research governance and management in the Western Pacific: A WHO Expert Consultation

Journal of Evidence-Based Medicine

Volumn 4, Issue 4, 2011, Pages 204-213

  Rani, Manju ^a   Bekedam, Hendrik ^a   Buckley, Brian S ^b  

^a WORLD HEALTH ORGANIZATION   (Switzerland)

^b UNIVERSITY OF THE PHILIPPINES MANILA   (Philippines)

Author keywords

[No Author keywords available]

Indexed keywords

CONSULTATION; HEALTH CARE POLICY; HEALTH CARE QUALITY; HUMAN; INVESTMENT; MEDICAL RESEARCH; NOTE; PRIORITY JOURNAL; REGISTRATION; RESEARCH ETHICS; WORLD HEALTH ORGANIZATION;

DATABASES, FACTUAL; ETHICS, RESEARCH; INVESTMENTS; REFERRAL AND CONSULTATION; REGISTRIES; RESEARCH; WORLD HEALTH ORGANIZATION;

EID: 82455184902     PISSN: 17565383     EISSN: 17565391     Source Type: Journal    
DOI: 10.1111/j.1756-5391.2011.01161.x     Document Type: Note

References (16)

1. The Report on the Commission on Health Research for Development: Health research. Essential Link to Equity in Development. Oxford Oxford University Press; 1990.
2. World Health organization. Report from the Ministerial Summit on Health Research (Mexico 2004). Geneva: World Health organization 2005.
3. World Health organization. Scaling up research and learning for health systems: now is the time: Report of a High Level Task Force, presented and endorsed at the Global Ministerial Forum on Research for Health 2008, Bamako, Mali Geneva: World Health Organization 2009.
4. Scherer RW, Langenberg P, von Elm E. Full publication of results initially presented in abstracts. Cochrane Database Systematic Reveiws. 2007(2): MR000005.
5. McGauran N, Wieseler B, Kreis J, Schuler YB, Kolsch H, Kaiser T. Reporting bias in medical research - a narrative review. Trials. 2010; 11: 37.
6. Chalmers I, Glasziou P. Avoidable waste in the production and reporting of research evidence. The Lancet. 2009; 374: 86-9.
7. Dear RF, Barratt AL, McGeechan K, Askie L, Simes J, Tattersall MHN. Landscape of cancer clinical trials in Australia: using trial registries to guide future research. Medical Journal of Australia. 2011; 194: 387-91.
8. Lim TO, Asmaliza SI, Goh PP, Michael AJ, Hon YK, Thandapani R, et al The National Medical Research Register - A vital link between Current and Future Research. Medical Journal of Malaysia. 2010; 65(Suppl A): 124-7.
9. Ghersi D, Pang T. From Mexico to Mali: four years in the history of clinical trial registration. Journal of Evidence Based Medicine 2009; 2: 1-7.
10. Hasselblatt H, Dreier G, Antes G, Schumacher M. The German Clinical Trials Register: challenges and chances of implementing a bilingual registry. Journal of Evidence Based Medicine. 2009; 2: 36-40.
11. Ghersi D, Pang T. En route to international clinical trial transparency. The Lancet. 2008; 372: 1531-2.
12. OECD Principles and Guidelines for Access to Research Data from Public Funding. Paris: Organisation for Economic Co-Operation and Development 2007.
13. Chan M, Kazatchkine M, Lob-Levyt J, Obaid T, Schweizer J, Sidibe M, et al Meeting the Demand for Results and Accountability: A Call for Action on Health Data from Eight Global Health Agencies. PLoS Medicine 2010; 7(1): e1000223.
14. Pisani E, Abou Zahr C. Sharing health data: good intentions are not enough. Bulletin of World Health Organization. 2010; 88: 462-6.
15. Pisani E, Whitworth J, Zaba B, Abou-Zahr C. Time for fair trade in research data. The Lancet. 2010; 375: 703-5.
16. Walport M, Brest P. Sharing research data to improve public health. The Lancet. 2011; 6736: 62234-9.