Engage to define patient centred outcomes
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Public Involvement Lead at the Health Research Authority
As Public Involvement Lead for the Health Research Authority in the UK I will enable the contribution patients make to the design of clinical studies to positively assure Research Ethics Committees that the studies will be acceptable to prospective participants and so help the review process
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Editor
I commit to thinking of patients first and last each time I communicate about health and medicine.
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I will work with potential study participants to create patient support materials/information that they feel is needed and helpful
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Founder/President
Making sure we have consulted the patients (e.g. via surveys & one-on-one conversations etc.) and their voices are embedded in all our activities.
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Founder/President
Giving patients the opportunity to engage in our activities.
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Founder/President
Making sure there’s a two-way communication loop, adding lay versions in as many languages as we can publish.
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Programs Director
I commit to practicing empathy and listening to new points of views and ideas without prejudice.
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