Engaging the Canadian public on reimbursement decision-making for drugs for rare diseases: a national online survey

Author:

Polisena Julie,Burgess Michael,Mitton Craig,Lynd Larry D.

Funder

Canadian Agency for Drugs and Technologies in Health

Canadian Institutes for Health Research

Publisher

Springer Science and Business Media LLC

Subject

Health Policy

Reference19 articles.

1. Richter T, Nestler-Parr S, Babela R, Khan ZM, Tesoro T, Molsen E, Hughes DA. Rare Disease Terminology and Definitions-A Systematic Global Review: Report of the ISPOR Rare Disease Special Interest Group. Value Health. 2015;18:906–14.

2. Menon D, Clark D, Stafinski T. Reimbursement of Drugs for Rare Diseases through the Public Healthcare System in Canada: Where Are We Now? Healthc Policy. 2015;11:15–32.

3. Loorand-Stiver L, Cowling T, Perras C. Drugs for rare diseases: evolving trends in regulatory and health technology assessment perspectives. Ottawa: CADTH; 2016.

4. Paulden M, Stafinski T, Menon D, McCabe C. Value-Based Reimbursement Decisions for Orphan Drugs: A Scoping Review and Decision Framework. Pharmacoeconomics. 2014;33(2):255–69.

5. Short H, Stafinski T, Menon D. A national approach to reimbursement decision-making on drugs for rare diseases in Canada? Insights from across the ponds. Healthc Policy. 2015;10:24–46.

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