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iConsent an Electronic Consent Platform with the MS Register

ABSTRACT Objectives The UK MS Register is a large scale observational research platform, capturing data from patients, NHS and carries out linkage with routine data from the SAIL databank. We have 14,000 People with MS (PwMS) submitting Patient Reported Outcome Measures (PRoMS) quarterly and o...

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Bibliografische gegevens
Hoofdauteurs: Rod Middleton, David Ford, Daniel Naeh
Formaat: Artigo
Taal:Inglês
Gepubliceerd in: Swansea University 2017-04-01
Reeks:International Journal of Population Data Science
Online toegang:https://ijpds.org/article/view/363
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