PRO Data Collection in Clinical Trials Using Mixed Modes: Report of the ISPOR PRO Mixed Modes Good Research Practices Task Force

Author:

Eremenco SonyaORCID,Coons Stephen Joel,Paty Jean,Coyne Karin,Bennett Antonia V.,McEntegart Damian

Publisher

Elsevier BV

Subject

Public Health, Environmental and Occupational Health,Health Policy

Reference37 articles.

1. US Food and Drug Administration. Guidance for industry: patient-reported outcome measures: use in medical product development to support labeling claims. 2009. Available from: http://www.fda.gov/downloads/Drugs/GuidanceComplianceRegulatoryInformation/Guidances/UCM193282.pdf. [Accessed June 1, 2014].

2. US Food and Drug Administration. Clinical Outcome Assessment Qualification Program. October 11, 2013 update. Available from: http://www.fda.gov/Drugs/DevelopmentApprovalProcess/DrugDevelopmentToolsQualificationProgram/ucm284077.htm. [Accessed June 1, 2014].

3. Walton MK, Powers JH, Hobart J, et al. Clinical outcomes assessments (COAs): a conceptual foundation. ISPOR ClinRO Task Force report. Value Health. In press.

4. US Food and Drug Administration. Measurement in clinical trials: review and qualification of clinical outcome assessments. In: Public Workshop; Silver Spring, MD; October 19, 2011. Available from: http://www.fda.gov/Drugs/NewsEvents/ucm276110.htm. [Accessed June 1, 2014].

5. Diary keeping in asthma: comparison of written and electronic methods;Hyland;BMJ,1993

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