Involving the Public in the Design and Conduct of
Research:
Building Research Partnerships
A virtual workshop for Researchers & Members of
the Public
What is it?
This free virtual workshop will look at practical ways to involve patients and the public as partners (PPI) in
the research process. It will explore the issues related to becoming and being a member of the public
involved in research and the role of researchers in facilitating this involvement.
Who is it for?
Patients, carers and members of the public who are interested in getting involved in research and
researchers interested in involving patients, carers and the public in their research.
How long is it?
2½ hour virtual workshop by zoom link.
What will I get out of it?
As a patient, carer or member of the public, you will gain an understanding of what it means
to be involved in research at each stage of the research process.
As a researcher, you will gain an understanding of how patients, carers and the public can
get involved in research, practical tips, the opportunity to share your research expertise and build
research partnerships.
Registration:
To register your interest for this workshop please complete the form below:
https://forms.office.com/Pages/ResponsePage.aspx?
id=DQSIkWdsW0yxEjajBLZtrQAAAAAAAAAAAAO__SFFNA1UQ1Q1RUJJNkJTQUE1SUJJRE9GVjFQT
FVJTC4u
Reviews from past participants:
It was all invaluable I liked the
format and the opportunity to
interact and ask questions.
The ability to share information in
a safe environment, within a small
group.
All the information was
appropriate and relevant. There
were good opportunities to ask
questions and interact with
attendees.
Having patients and service users there
for the dragon's den element to
actually hear what they thought of our
projects was an excellent addition.
Really enjoyable discussion and tips to
recruit were excellent.