This year our focus groups discussed the importance and use of data in the Parkinson's research arena:

  • How we can collect relevant data from people with Parkinson's with the quality and in the quantity required to allow experiences to drive the research agenda?
  • How do we engage sufficient numbers of people with Parkinson’s in recording information about themselves?
  • What controls do we need in place?

This meeting is an important annual event in The Cure Parkinson's Trust calendar. See the results of the survey and conclusions drawn here.

Booking for this event has now closed.