Literature DB >> 23672750

Improving health research governance and management in the Western Pacific: a WHO expert consultation.

Manju Rani1, Hendrik Bekedam, Brian S Buckley.   

Abstract

Repeated calls have been made in recent decades to increase investments in health research, especially in low- and middle-income countries (LMIC). However, the perceived low relevance and quality of health research, poor visibility of outputs, and difficulties in tracking current levels of and returns on investments have undermined efforts to advocate for additional investments in these countries. Some of these issues emanate from inadequate governance and management systems for health research at the national level, which are ineffective in tracking and steering the research portfolio and investments, ensuring quality, and facilitating access to research outputs. In spite of this, the value, necessity, and cost of performing health research management and governance functions are not well appreciated, especially in LMIC. To address this, the World Health Organization (WHO) Regional Office for the Western Pacific organized an expert consultation in August 2011, involving experts from 14 of its developed and developing member states and from leading research organizations such as the Wellcome Trust. The consultation identified essential health research governance and management functions that must be performed by appropriate organizational entities to maximize returns on health research investments. In addition, three specific areas for intervention were considered: (1) prospective research registration in publicly accessible national health research registries; (2) systematic health research data archiving and wider access; and (3) national research ethics systems. A consensus was reached on the need to invest more in essential health research and management functions, including establishing publicly accessible web-based national health research registries for prospective registration of health research, setting up systems to archive and share health research data, and improving the governance of research ethics committees. The consultation also concluded that the costs of performing these functions are legitimate and necessary research costs that must be shouldered by research funding organizations.
© 2011 Blackwell Publishing Asia Pty Ltd and Chinese Cochrane Center, West China Hospital of Sichuan University.

Mesh:

Year:  2011        PMID: 23672750     DOI: 10.1111/j.1756-5391.2011.01161.x

Source DB:  PubMed          Journal:  J Evid Based Med        ISSN: 1756-5391


  14 in total

1.  Strengthening research governance for sustainable research: experiences from three Zimbabwean universities.

Authors:  Thokozile Mashaah; James Hakim; Midion Chidzonga; Rugare A Kangwende; Yogeshkumar Naik; Nancy Federspiel; Suzanne Fiorillo; Jim Scott; Exnevia Gomo
Journal:  Acad Med       Date:  2014-08       Impact factor: 6.893

2.  Parental and professional perceptions of informed consent and participation in a time-critical neonatal trial: a mixed-methods study in India, Sri Lanka and Bangladesh.

Authors:  Stuti Pant; Maya Annie Elias; Kerry Woolfall; Maria Moreno Morales; Bensitta Lincy; Ismat Jahan; Samanmali P Sumanasena; Siddarth Ramji; Seetha Shankaran; Sudhin Thayyil
Journal:  BMJ Glob Health       Date:  2021-05

3.  Sharing Public Health Research Data: Toward the Development of Ethical Data-Sharing Practice in Low- and Middle-Income Settings.

Authors:  Michael Parker; Susan Bull
Journal:  J Empir Res Hum Res Ethics       Date:  2015-07       Impact factor: 1.742

4.  Sweat, Skepticism, and Uncharted Territory: A Qualitative Study of Opinions on Data Sharing Among Public Health Researchers and Research Participants in Mumbai, India.

Authors:  Ketaki Hate; Sanna Meherally; Neena Shah More; Anuja Jayaraman; Susan Bull; Michael Parker; David Osrin
Journal:  J Empir Res Hum Res Ethics       Date:  2015-07       Impact factor: 1.742

5.  Perceived Benefits, Harms, and Views About How to Share Data Responsibly: A Qualitative Study of Experiences With and Attitudes Toward Data Sharing Among Research Staff and Community Representatives in Thailand.

Authors:  Phaik Yeong Cheah; Decha Tangseefa; Aimatcha Somsaman; Tri Chunsuttiwat; François Nosten; Nicholas P J Day; Susan Bull; Michael Parker
Journal:  J Empir Res Hum Res Ethics       Date:  2015-07       Impact factor: 1.742

Review 6.  Views of Ethical Best Practices in Sharing Individual-Level Data From Medical and Public Health Research: A Systematic Scoping Review.

Authors:  Susan Bull; Nia Roberts; Michael Parker
Journal:  J Empir Res Hum Res Ethics       Date:  2015-07       Impact factor: 1.742

7.  Involving Research Stakeholders in Developing Policy on Sharing Public Health Research Data in Kenya: Views on Fair Process for Informed Consent, Access Oversight, and Community Engagement.

Authors:  Irene Jao; Francis Kombe; Salim Mwalukore; Susan Bull; Michael Parker; Dorcas Kamuya; Sassy Molyneux; Vicki Marsh
Journal:  J Empir Res Hum Res Ethics       Date:  2015-07       Impact factor: 1.742

8.  Developing data elements for research information system in health; a starting point for systems integration.

Authors:  Nr Ghorbani; M Ahmadi; F Sadoughi; M Ghanei
Journal:  Iran J Public Health       Date:  2012-12-01       Impact factor: 1.429

9.  Research Stakeholders' Views on Benefits and Challenges for Public Health Research Data Sharing in Kenya: The Importance of Trust and Social Relations.

Authors:  Irene Jao; Francis Kombe; Salim Mwalukore; Susan Bull; Michael Parker; Dorcas Kamuya; Sassy Molyneux; Vicki Marsh
Journal:  PLoS One       Date:  2015-09-02       Impact factor: 3.240

Review 10.  Best Practices for Ethical Sharing of Individual-Level Health Research Data From Low- and Middle-Income Settings.

Authors:  Susan Bull; Phaik Yeong Cheah; Spencer Denny; Irene Jao; Vicki Marsh; Laura Merson; Neena Shah More; Le Nguyen Thanh Nhan; David Osrin; Decha Tangseefa; Douglas Wassenaar; Michael Parker
Journal:  J Empir Res Hum Res Ethics       Date:  2015-07       Impact factor: 1.742

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