Community and Patient Preference Research (CaPPRe)’s Post

Last day to register for tomorrow's webinar with Patient Voice Initiative! So many great speakers and topics lined up, including: ✔️ How patient-based evidence is different to participation - Ann Single ✔️ The importance of qualitative insights- Jenni G. (CaPPRe) & Clare Stuart (Mito Foundation) ✔️ How do we better include different communities, e.g., with cognitive impairment, into research? - Ann Single (PVI) & Sarah Jay (Dementia Australia) ✔️What patient preferences are and partnering with a patient organisation- Simon Fifer (CaPPRe) & Brent Clifton (NAPWHA) ✔️Wrap up & close - Jessica Bean (PVI) & Cathy Sertori (MC) Click the link to register below ⬇️

Developing patient-based evidence: Introduction for patient organisations

Developing patient-based evidence: Introduction for patient organisations

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