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Found 63 results.

Searching for: Authors starting with M

Patients participating as co-researchers in health research: A systematic review of outcomes and experiences.

Malterud K & Elvbakken KT
Scandinavian Journal of Public Health. Epub ahead of print doi: 10.1177/1403494819863514.
Added: 28 November 2019

How and Why to Involve Patients in Drug Development: Perspectives From the Pharmaceutical Industry, Regulatory Authorities, and Patient Organisations.

Marianne Botoft Hansen, Lotte Stig Nørgaard, Christine Erikstrup Hallgreen.
Therapeutic Innovation & Regulatory Science. 1-9.
Added: 21 October 2019

Ethical Challenges Related to Patient Involvement in Health Technology Assessment.

Meredith Vanstone, Julia Abelson, Julia Bidonde, Kenneth Bond, Raquel Burgess, Carolyn Canfield, Lisa Schwartz and Laura Tripp.
International Journal of Technology Assessment in Health Care Epub DOI: https://doi.org/10.1017/S0266462319000382
Added: 30 July 2019

Patient and public involvement: Two sides of the same coin or different coins altogether?

Matthew S. McCoy, Jonathan Warsh, Leah Rand, Michael Parker, Mark Sheehan.
Bioethics, 1-8. [Epub ahead of print] doi.org/10.1111/bioe.12584
Added: 09 July 2019

Practical guidance for patient-centred health research.

Maarten de Wit, Cyrus Cooper, Jean-Yves Reginster on behalf of the WHO-ESCEO Working Group.
The Lancet, VOLUME 393, ISSUE 10176, P1095-1096, MARCH 16, 2019.
Added: 09 July 2019

Disentangling patient and public involvement in healthcare decisions: why the difference matters.

Mio Fredriksson, Jonathan Q. Tritter.
Sociology of Health & Illness, 39(1), 95-111.
Added: 09 July 2019

Power dynamics and collaborative mechanisms in co-production and co-design processes.

Michelle Farr
Critical Social Policy, 38(4), 623–644. 
Added: 08 April 2019

Practical guidance for patient-centred health research.

Maarten de Wit, Cyrus Cooper, Jean-Yves Reginster on behalf of the WHO-ESCEO Working Group.
The Lancet, 393(10176), 1095-1096.
Added: 08 April 2019

Consensus Statement on Public Involvement and Engagement with Data-Intensive Health Research.

Mhairi Aitken, Mary P Tully, Carol Porteous, Simon Denegri, Sarah Cunningham-Burley, Natalie Banner, Corri Black, Michael Burgess, Lynsey Cross, Johannes van Delden ,Elizabeth Ford, Sarah Fox, Natalie Fitzpatrick, Kay Gallacher, Catharine Goddard, Lamiece Hassan, Ron Jamieson, Kerina H Jones, Minna Kaarakainen, Fiona Lugg-Widger, Kimberlyn McGrail, Anne McKenzie, Rosalyn Moran, Madeleine J Murtagh, Malcolm Oswald, Alison Paprica, Nicola Perrin, Emma Victoria Richards, John Rouse, Joanne Webb, Donald J Willison.
International Journal of Population Data Science, 4:1:06
Added: 18 March 2019

Strength in Numbers: an international consensus conference to develop a novel approach to care delivery for young adults with type 1 diabetes, the D1 Now Study.

M. C. O’Hara, L. Hynes, M. O’Donnell, C. Keighron, G. Allen, A. Caulfield, C. Duffy, M. Long, M. Mallon, M. Mullins, G. Tonra, M. Byrne, S. F. Dinneen and with the D1 Now Type 1 Diabetes Young Adult Study Group.
Research Involvement and Engagement 3:25
Added: 04 March 2019