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Patient Perspectives on the Value of Patient Preference Information in Regulatory Decision Making: A Qualitative Study in Swedish Patients with Rheumatoid Arthritis.

Research output: Contribution to journalArticleAcademic

11 Citations (Scopus)
21 Downloads (Pure)
Original languageEnglish
Pages (from-to)297-305
Number of pages9
JournalThe patient: Patient-Centered Outcomes Research
Volume12
Issue number3
DOIs
Publication statusPublished - 2019

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