Mixed-methods evaluation of the NHS Genomic Medicine Service for paediatric rare diseases: study protocol.
Celine LewisJames BuchananAngus John ClarkeEmma ClementBettina FriedrichJillian Hastings-WardMelissa HillRuth HornAnneke M LucassenChristine PatchAlexandra PickardLauren RobertsSaskia C SandersonSarah L WynnCecilia Vindrola-PadrosMonica LakhanpaulPublished in: NIHR open research (2021)
We will disseminate our results to policymakers as findings emerge, so any suggested changes to service provision can be considered in a timely manner. A workshop with key stakeholders will be held in Year 4 to develop and agree a set of recommendations for practice.