blank
blank

Strategies for diversity and inclusion in public involvement

1:1
Supplement to the briefing notes for researchers

This supplement provides ideas and information to support the involvement of a wide range of people in research and to identify ways to reach out to members of the public who do not often get involved in research.

Acces this publication (pdf)

You might also be interested in

Involving and engaging ‘seldom listened to’ community voices in clinical translational health research: a social innovation approach

“We are not hard to reach, but we may find it hard to trust”

Everyday Words for Public Health Communication

Inclusive Involvement: Practical Steps You Can Take Today

A Friendly Guide to Equality, Diversity & Inclusion (EDI) Equality, Diversity & Inclusion (EDI) Equality, Diversity & Inclusion (EDI) in Public and Patient Involvement (PPI)

Patient Partner Compensation Guidelines

"Patient partner" is an overarching term that includes individuals with lived experience, including patients, caregivers, family, and friends.

ERDERA's

search form