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Section links:

PPI Home

Aims and Objectives

Background

Co-ordination of Patient and Public Involvement

PPI documents

PPI forum

Principles

What does PPI mean?

PPI Working Group

Registering your interest pdf file

 


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Co-ordinating Patient and Public Involvement

The co-ordination of patient and public involvement presents a particular challenge for DeNDRoN. There are a number of issues which need to be addressed to enable people affected by these dieases to become more actively involved in research. Although many of these issues cut across all the diseases incorporated into the Dementias & Neurodegenerative Diseases Research Network, there are also issues specific to each disease. We are in the process of developing our strategy for coordinating PPI across the network. This strategy will combine tackling cross cutting issues with providing disease-specific support where appropriate. We are currently developing this strategy in conjunction with our non-statutory disease association partners, and with the UKCRN and Department of Health.

The DeNDRoN Co-ordinating Centre has appointed an officer to act as the coordinator of the patient and public involvement programme. The post holder is responsible for using the road map to develop and deliver our patient and public involvement programme.

 

 

 

 

 



London Office (General Enquiries)
DeNDRoN Co-ordinating Centre
Wolfson Centre
Mecklenburgh Square
LONDON
WC1N 2AP

Tel: +44 (0)20 7905 2995
Fax: +44 (0)20 7905 2959



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Newcastle Office (Portfolio Enquiries)
Wolfson Research Centre
Institute for Ageing and Health
Newcastle University
Campus for Ageing and Vitality
NEWCASTLE UPON TYNE
NE4 5PL
Tel:  +44 (0)191 248 1347
Fax: +44 (0)191 248 1301

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