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1138819
registered interest false more like this
date remove filter
answering body
Department of Health and Social Care more like this
answering dept id 17 remove filter
answering dept short name Health and Social Care more like this
answering dept sort name Health and Social Care more like this
hansard heading Health Services: Technology more like this
house id 1 more like this
legislature
25259
pref label House of Commons more like this
question text To ask the Secretary of State for Health and Social Care, what steps he will take to ensure the broadest number of patient groups can participate in the National Institute for Health and Care Excellence’s review of health technology assessment methods and processes. more like this
tabling member constituency Scunthorpe more like this
tabling member printed
Nic Dakin more like this
uin 277172 more like this
answer
answer
is ministerial correction false more like this
date of answer less than 2019-07-23more like thismore than 2019-07-23
answer text <p>There are three patient/lay representatives on the methods working group with a wide range of experience, covering a range of topic areas, reflecting the programmes under review. Two of the patient/lay representatives also belong to the Patients Involved in NICE coalition.</p><p>Patient groups will be involved in the review of each of the specific methodological areas as detailed in the paper presented to the NICE board on 17 July 2019. Experts in the area will be invited to participate in topic specific methods task and finish groups.</p><p>NICE has established a dedicated patient working group. There are six patient organisation representatives on the group, including those who belong to the Patients Involved in NICE coalition. The group will work directly with patient/carer groups to coordinate the patient perspective on both methods and process. A stakeholder workshop with patient groups was held in January 2019 that included representatives from 22 patient organisations.</p><p>The patient working group has recently disseminated a survey to patient umbrella groups to develop a clear understanding of the patient perspective on both methods and processes. The survey runs until 5pm on Monday 12 August 2019. It will be promoted via social media and sent directly to groups working with NICE. Patient organisations can communicate with representatives on the methods working group and patient working group outside of this survey.</p><p>Patient organisations will have the opportunity to comment directly on proposals during the public consultation in summer 2020.</p><p>NICE is implementing other opportunities to encourage more patient group involvement throughout the review via provision of a subscription based bulletin for updates and information (which people can subscribe to via their website) and exploring arrangements of additional engagement sessions (i.e. webinars), as and when appropriate.</p><p> </p>
answering member constituency South Ribble more like this
answering member printed Seema Kennedy more like this
grouped question UIN
277170 more like this
277171 more like this
question first answered
less than 2019-07-23T16:34:14.72Zmore like thismore than 2019-07-23T16:34:14.72Z
answering member
4455
label Biography information for Seema Kennedy more like this
tabling member
4056
label Biography information for Nic Dakin more like this
1138859
registered interest false more like this
date remove filter
answering body
Department of Health and Social Care more like this
answering dept id 17 remove filter
answering dept short name Health and Social Care more like this
answering dept sort name Health and Social Care more like this
hansard heading Genetics: Screening more like this
house id 1 more like this
legislature
25259
pref label House of Commons more like this
question text To ask the Secretary of State for Health and Social Care, with reference to the Clinical Advisory Group for Genomics, if he will set out (a) its terms of reference, (b) when it will first meet, (c) how patient voice will be incorporated into its work, (d) who it will report to and (e) when the (i) Commissioning Policy for Preimplantation Genetic Diagnosis review and (ii) other work of its predecessor, the Clinical Reference Group for Medical Genetics, will be completed; and if he will make a statement. more like this
tabling member constituency Hornsey and Wood Green more like this
tabling member printed
Catherine West more like this
uin 277243 more like this
answer
answer
is ministerial correction false more like this
date of answer less than 2019-07-23more like thismore than 2019-07-23
answer text <p>NHS England has paused the recruitment for the clinical genetics clinical reference group to ensure the right advisory groups are in place to provide clinical advice across the breadth and depth of the future NHS Genomic Medicine Service.</p><p>These new arrangements will need consider clinical genetics and genetic counselling, but also wider implications of genomics for the National Health Service. Any future arrangements will have appropriate representation, including patient and public voices.</p><p>NHS England is progressing the clinical commissioning policy for Preimplantation Genetic Diagnosis (PGD). This work will include assessment of the treatment pathways for existing PGD services and consideration of the ethical issues. NHS England will continue to seek input from clinicians and patients throughout this work.</p> more like this
answering member constituency Gosport more like this
answering member printed Caroline Dinenage more like this
question first answered
less than 2019-07-23T16:06:02.047Zmore like thismore than 2019-07-23T16:06:02.047Z
answering member
4008
label Biography information for Dame Caroline Dinenage more like this
tabling member
4523
label Biography information for Catherine West more like this
1138879
registered interest false more like this
date remove filter
answering body
Department of Health and Social Care more like this
answering dept id 17 remove filter
answering dept short name Health and Social Care more like this
answering dept sort name Health and Social Care more like this
hansard heading Audiology and Hearing Aids more like this
house id 1 more like this
legislature
25259
pref label House of Commons more like this
question text To ask the Secretary of State for Health and Social Care, pursuant to the Answer on 12 June 2019 to Question 260081, whether his Department will require Clinical Commissioning Groups to collect and publish data in a comparable form on (a) the amount spent on audiology services, (b) the number of hearing aids fitted and (c) outcomes of hearing aid fittings. more like this
tabling member constituency North Tyneside more like this
tabling member printed
Mary Glindon more like this
uin 277193 more like this
answer
answer
is ministerial correction false more like this
date of answer less than 2019-07-23more like thismore than 2019-07-23
answer text <p>Clinical commissioning groups (CCGs) are responsible for the collection and collation of audiology data to enable them to manage regional needs. NHS England has no plans to mandate CCGs to collect or publish their data in a comparable form.</p> more like this
answering member constituency Gosport more like this
answering member printed Caroline Dinenage more like this
question first answered
less than 2019-07-23T16:03:42.847Zmore like thismore than 2019-07-23T16:03:42.847Z
answering member
4008
label Biography information for Dame Caroline Dinenage more like this
tabling member
4126
label Biography information for Mary Glindon more like this