1. Incorporating the patient experience into regulatory decision making in the USA, Europe, and Canada

2. US Department of Health and Human Services, Food and Drug Administration, Center for Devices and Radiological Health, Center for Biologics Evaluation and Research. Guidance for Industry: Patient Preference Information – Voluntary Submission, Review in Premarket Approval Applications, Humanitarian Device Exemption Applications, and De Novo Requests, and Inclusion in Decision Summaries and Device Labeling; 2016.

3. healthcare Ifqaei. Background: what are patient preferences? Accessed 24 June, 2019.

4. UK R. NICE given grant to research patient preference; 2016. Accessed 24 June, 2019.