Open access book by 120+ authors (including 3 out of 4 chapters with a patient author) on how participation and research into patient aspects (needs, preferences, experiences and perspectives) improves processes to guide decisions about the funding of healthcare (such as medicines and tests).
 
It covers:
  • Concepts
  • Methods
  • Examples.
Chapters: HTA, Justice rationales, Research into patient aspects, Participation, Evidence co-creation, Social media research, Patient preferences research, Ethnographic fieldwork, Qualitative evidence synthesis, Evaluation, Australia, Belgium, Czechia, England, European Union, Germany, Latin America and Caribbean, The Philippines, Republic of Korea, Singapore, Spain, Taiwan, USA, Wales & perspectives from Low and Middle Income Countries, HTA Committee Chair, Medicine and Medical Technology Developers (Industry), Patient Organisations, plus Discussion chapters and Seven Calls to Action.

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