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Genetic Alliance UK
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Policy
Protect European Reference Networks
eu
Resetting the model
policy
Patient Charter on Newborn Screening
policy
THE NICE TECHNOLOGY APPRAISAL PROGRAMME: OUR RESPONSE
policy
Responses to Parliamentary Inquiries: Brexit and Genome Editing
parliamentary
Patient and public involvement at NICE
policy
Genomics and genome-editing inquiry evidence
parliamentary
Pledge for Patients 2015-16
uk
Webinar: Proposed changes to the appraisal of specialised treatments
uk
Individual patient funding requests in Wales
wales
Abortion (Disability Equality) Bill briefing
parliamentary
All Party Parliamentary Group hearing on access to medicines in England
parliamentary
Research on non-invasive prenatal testing
research
The benefits of EU membership for our community
policy
Cancer patients’ views on genome sequencing
research
Public perspectives on neuro-enhancement
research
Access to medicines for rare diseases in Scotland
policy
On Wednesday 23 March 2016, we launched our new Patient […]
My Condition, My DNA
policy
The Genomics Conversation
research
Mitochondrial donation regulation consultation
policy
Use of animals in medical research
research
NHS England’s commissioning of medicines for rare diseases
policy
NICE’s evaluation of highly specialised technologies
policy
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