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1682680
registered interest false more like this
date less than 2024-01-16more like thismore than 2024-01-16
answering body
Department of Health and Social Care remove filter
answering dept id 17 more like this
answering dept short name Health and Social Care more like this
answering dept sort name Health and Social Care more like this
hansard heading Medicines and Medical Devices Safety Independent Review remove filter
house id 2 more like this
legislature
25277
pref label House of Lords more like this
question text To ask His Majesty's Government what assessment they have made of the Independent Medicines and Medical Devices Safety Review report First Do No Harm, published on 8 July 2020. more like this
tabling member printed
Baroness Ritchie of Downpatrick more like this
uin HL1650 more like this
answer
answer
is ministerial correction false more like this
date of answer less than 2024-01-24more like thismore than 2024-01-24
answer text <p>The Independent Medicines and Medical Devices Safety (IMMDS) Review was clear in its finding that the healthcare system failed to listen to patients’ concerns on the issues covered by the review. The Government’s 2021 response to the review set out which of the review’s recommendations the Government had accepted. We also published an update in an online-only format in December 2022 setting out progress made against those recommendations, which includes appointing the first ever Patient Safety Commissioner in England to champion patients’ voices in relation to the safety of medicines and medical devices. In April 2023, the Government also responded to the recommendations made by the Health and Social Care Committee in its report ‘Follow-up on the IMMDS report and the Government’s response’, published in January 2023. A copy of the follow-up report is attached.</p> more like this
answering member printed Lord Markham more like this
grouped question UIN HL1651 more like this
question first answered
less than 2024-01-24T12:10:36.82Zmore like thismore than 2024-01-24T12:10:36.82Z
answering member
4948
label Biography information for Lord Markham more like this
attachment
1
file name IMMDS follow-up report (1).pdf more like this
title IMMDS follow-up report more like this
tabling member
4130
label Biography information for Baroness Ritchie of Downpatrick more like this
1682681
registered interest false more like this
date less than 2024-01-16more like thismore than 2024-01-16
answering body
Department of Health and Social Care remove filter
answering dept id 17 more like this
answering dept short name Health and Social Care more like this
answering dept sort name Health and Social Care more like this
hansard heading Medicines and Medical Devices Safety Independent Review remove filter
house id 2 more like this
legislature
25277
pref label House of Lords more like this
question text To ask His Majesty's Government when they intend to implement all of the recommendations contained in the Independent Medicines and Medical Devices Safety Review report First Do No Harm, published on 8 July 2020. more like this
tabling member printed
Baroness Ritchie of Downpatrick more like this
uin HL1651 more like this
answer
answer
is ministerial correction false more like this
date of answer less than 2024-01-24more like thismore than 2024-01-24
answer text <p>The Independent Medicines and Medical Devices Safety (IMMDS) Review was clear in its finding that the healthcare system failed to listen to patients’ concerns on the issues covered by the review. The Government’s 2021 response to the review set out which of the review’s recommendations the Government had accepted. We also published an update in an online-only format in December 2022 setting out progress made against those recommendations, which includes appointing the first ever Patient Safety Commissioner in England to champion patients’ voices in relation to the safety of medicines and medical devices. In April 2023, the Government also responded to the recommendations made by the Health and Social Care Committee in its report ‘Follow-up on the IMMDS report and the Government’s response’, published in January 2023. A copy of the follow-up report is attached.</p> more like this
answering member printed Lord Markham more like this
grouped question UIN HL1650 more like this
question first answered
less than 2024-01-24T12:10:36.777Zmore like thismore than 2024-01-24T12:10:36.777Z
answering member
4948
label Biography information for Lord Markham more like this
attachment
1
file name IMMDS follow-up report (1).pdf more like this
title IMMDS follow-up report more like this
tabling member
4130
label Biography information for Baroness Ritchie of Downpatrick more like this
1564490
registered interest false more like this
date less than 2023-01-06more like thismore than 2023-01-06
answering body
Department of Health and Social Care remove filter
answering dept id 17 more like this
answering dept short name Health and Social Care more like this
answering dept sort name Health and Social Care more like this
hansard heading Medicines and Medical Devices Safety Independent Review remove filter
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 Section 9 Conflicts of interest in the Policy paper entitled Independent Medicines and Medical Devices Safety Review: update report on government implementation, published on 22 December 2022, and the Patient Representative Working Group, what patient groups were represented on that Working Group; how those patient groups were chosen and by whom; how many people in total were in the Working Group; and how many times the Working Group had met as on 6 January 2023. more like this
tabling member constituency Kingston upon Hull West and Hessle more like this
tabling member printed
Emma Hardy more like this
uin 117892 more like this
answer
answer
is ministerial correction false more like this
date of answer less than 2023-01-16more like thismore than 2023-01-16
answer text <p>The Department selected patient representatives through engagement with NHS England and the Devolved Governments. Our intention was to form a voluntary group that best represented patients across the four nations. Since March 2022, we have held two Patient Representative Groups (PRG). Four patient representatives attended each of the sessions. We expect to hold another PRG early in 2023 to discuss feedback on pilot systems.</p> more like this
answering member constituency Lewes more like this
answering member printed Maria Caulfield more like this
question first answered
less than 2023-01-16T11:10:45.34Zmore like thismore than 2023-01-16T11:10:45.34Z
answering member
4492
label Biography information for Maria Caulfield more like this
tabling member
4645
label Biography information for Emma Hardy more like this
1548642
registered interest false more like this
date less than 2022-12-05more like thismore than 2022-12-05
answering body
Department of Health and Social Care remove filter
answering dept id 17 more like this
answering dept short name Health and Social Care more like this
answering dept sort name Health and Social Care more like this
hansard heading Medicines and Medical Devices Safety Independent Review remove filter
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, if he will provide an update on plans for financial redress for those harmed by (a) mesh implants, (b) Primodos and (c) Sodium Valproate. more like this
tabling member constituency Enfield North more like this
tabling member printed
Feryal Clark more like this
uin 103060 more like this
answer
answer
is ministerial correction false more like this
date of answer less than 2022-12-13more like thismore than 2022-12-13
answer text <p>The Government’s response to the Independent Medicines and Medical Devices Safety Review did not accept the recommendation to establish separate redress schemes. We have worked with NHS Resolution to launch online claims gateways to support patients who may wish to bring a clinical negligence claim in relation to pelvic mesh and sodium valproate. We are improving the safety of medicines and medical devices through high standards for industry to market and manufacture products with the aim of reducing harm in future.</p> more like this
answering member constituency Lewes more like this
answering member printed Maria Caulfield more like this
question first answered
less than 2022-12-13T11:44:53.957Zmore like thismore than 2022-12-13T11:44:53.957Z
answering member
4492
label Biography information for Maria Caulfield more like this
tabling member
4822
label Biography information for Feryal Clark more like this
1434001
registered interest false more like this
date less than 2022-02-22more like thismore than 2022-02-22
answering body
Department of Health and Social Care remove filter
answering dept id 17 more like this
answering dept short name Health and Social Care more like this
answering dept sort name Health and Social Care more like this
hansard heading Medicines and Medical Devices Safety Independent Review remove filter
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 his Department plans to take in response to the letter to the Parliamentary Under-Secretary of State from Marie Lyon, Association for Children Damaged By HPT, Kath Sansom, Sling The Mesh, Emma Murphy and Janet Williams, In-Fact, on behalf of people damaged by vaginal mesh, sodium valproate and Primodos on the implementation of the recommendations of the Independent Medicines and Medical Devices Safety Review 2020 led by Baroness Cumberlege. more like this
tabling member constituency New Forest East more like this
tabling member printed
Dr Julian Lewis more like this
uin 127247 more like this
answer
answer
is ministerial correction false more like this
date of answer less than 2022-03-21more like thismore than 2022-03-21
answer text <p>The Department’s central correspondence team have no record of receiving this letter. We would be happy to respond formally if the letter could be re-sent to the Department.</p><p>The Government’s response to the Independent Medicines and Medical Devices Safety Review accepted the majority of the nine strategic recommendations and 50 actions for improvement. The recommendations and actions for improvement included vaginal mesh and sodium valproate. We aim to publish an update on implementation of the accepted recommendations in the summer.</p> more like this
answering member constituency Lewes more like this
answering member printed Maria Caulfield more like this
question first answered
less than 2022-03-21T10:35:36.31Zmore like thismore than 2022-03-21T10:35:36.31Z
answering member
4492
label Biography information for Maria Caulfield more like this
previous answer version
53279
answering member constituency Lewes more like this
answering member printed Maria Caulfield more like this
answering member
4492
label Biography information for Maria Caulfield more like this
tabling member
54
label Biography information for Sir Julian Lewis more like this
1353130
registered interest false more like this
date less than 2021-09-06more like thismore than 2021-09-06
answering body
Department of Health and Social Care remove filter
answering dept id 17 more like this
answering dept short name Health and Social Care more like this
answering dept sort name Health and Social Care more like this
hansard heading Medicines and Medical Devices Safety Independent Review remove filter
house id 2 more like this
legislature
25277
pref label House of Lords more like this
question text To ask Her Majesty's Government what plans they have to reconsider their response to the recommendation in the report of the Independent Medicines and Medical Devices Safety Review First do no harm, published on 8 July 2020, that separate schemes should be set up to meet the cost of providing additional care and support to those who have experienced avoidable harm from hormone pregnancy tests, valproate and pelvic mesh interventions. more like this
tabling member printed
Lord Hunt of Kings Heath more like this
uin HL2426 more like this
answer
answer
is ministerial correction false more like this
date of answer less than 2021-09-29more like thismore than 2021-09-29
answer text <p>The Government did not accept this recommendation and there are no plans to reconsider this response. Our priority is to make medicines and devices safer and we are pursuing a wide range of activity to further this aim. The response explains the changes that have been put in place since the Independent Medicines and Medical Devices Safety Review report’s publication and the further action the Government will take to implement the recommendations accepted and to improve patient safety.</p> more like this
answering member printed Lord Kamall more like this
question first answered
less than 2021-09-29T15:25:07.89Zmore like thismore than 2021-09-29T15:25:07.89Z
answering member
4909
label Biography information for Lord Kamall more like this
tabling member
2024
label Biography information for Lord Hunt of Kings Heath more like this
1349328
registered interest false more like this
date less than 2021-07-21more like thismore than 2021-07-21
answering body
Department of Health and Social Care remove filter
answering dept id 17 more like this
answering dept short name Health and Social Care more like this
answering dept sort name Health and Social Care more like this
hansard heading Medicines and Medical Devices Safety Independent Review remove filter
house id 2 more like this
legislature
25277
pref label House of Lords more like this
question text To ask Her Majesty's Government, further to the report by the Independent Medicines and Medical Devices Safety Review First do No Harm, published on 8 July 2020, what negotiations have taken place between the Department of Health and Social Care and Her Majesty’s Treasury about redress for those who have suffered harm from (1) Primodos, (2) sodium valproate, and (3) pelvic mesh. more like this
tabling member printed
Baroness Cumberlege more like this
uin HL2261 more like this
answer
answer
is ministerial correction false more like this
date of answer less than 2021-08-03more like thismore than 2021-08-03
answer text <p>The Department engaged with HM Treasury on redress prior to cross-Government approval of the response to the Independent Medicines and Medical Devices Safety Review.</p> more like this
answering member printed Lord Bethell more like this
question first answered
less than 2021-08-03T11:50:32.337Zmore like thismore than 2021-08-03T11:50:32.337Z
answering member
4708
label Biography information for Lord Bethell more like this
tabling member
2729
label Biography information for Baroness Cumberlege more like this
1346824
registered interest false more like this
date less than 2021-07-14more like thismore than 2021-07-14
answering body
Department of Health and Social Care remove filter
answering dept id 17 more like this
answering dept short name Health and Social Care more like this
answering dept sort name Health and Social Care more like this
hansard heading Medicines and Medical Devices Safety Independent Review remove filter
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 report of the Independent Medicines and Medical Devices Safety Review report entitled First Do No Harm, published in July 2020, what recent steps he has taken to progress implementation of recommendation five of that report on the rollout of specialist centres. more like this
tabling member constituency Meriden more like this
tabling member printed
Saqib Bhatti more like this
uin 33365 more like this
answer
answer
is ministerial correction false more like this
date of answer less than 2021-07-20more like thismore than 2021-07-20
answer text <p>As of April 2021, eight National Health Service trusts are working with NHS England and NHS Improvement to provide specialised services for women with complications of mesh inserted for urinary incontinence and vaginal prolapse. We continue to consider specialist centres for those adversely affected by medicines taken during pregnancy. Further detail on this recommendation will be included in the full response to the report to be published this year.</p> more like this
answering member constituency Mid Bedfordshire more like this
answering member printed Ms Nadine Dorries more like this
question first answered
less than 2021-07-20T15:33:34.677Zmore like thismore than 2021-07-20T15:33:34.677Z
answering member
1481
label Biography information for Ms Nadine Dorries more like this
tabling member
4818
label Biography information for Saqib Bhatti more like this
1346825
registered interest false more like this
date less than 2021-07-14more like thismore than 2021-07-14
answering body
Department of Health and Social Care remove filter
answering dept id 17 more like this
answering dept short name Health and Social Care more like this
answering dept sort name Health and Social Care more like this
hansard heading Medicines and Medical Devices Safety Independent Review remove filter
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 report of the Independent Medicines and Medical Devices Safety Review report entitled First Do No Harm, published in July 2020, what recent steps he has taken to progress implementation of recommendation seven of that report on establishing a central patient-identifiable database. more like this
tabling member constituency Meriden more like this
tabling member printed
Saqib Bhatti more like this
uin 33366 more like this
answer
answer
is ministerial correction false more like this
date of answer less than 2021-07-22more like thismore than 2021-07-22
answer text <p>NHS Digital has put together a programme of work to establish an information system to collect information on surgical implants and devices from healthcare providers in England, currently focussed on pelvic floor, or mesh and related procedures, as a priority.</p><p>This will be followed by the development of a United Kingdom-wide Medical Device Information System (MDIS) with regulations being made under section 19 of the Medicines and Medical Devices Act 2021. This system will mean that in future, subject to regulations, we can routinely collect medical device, procedure and outcome data from public and private provider organisations across the UK and data submitted directly from patients. Formal public consultation on the MDIS regulations will begin later this year with the aim of laying the regulations in due course.</p> more like this
answering member constituency Mid Bedfordshire more like this
answering member printed Ms Nadine Dorries more like this
question first answered
less than 2021-07-22T15:03:45.033Zmore like thismore than 2021-07-22T15:03:45.033Z
answering member
1481
label Biography information for Ms Nadine Dorries more like this
tabling member
4818
label Biography information for Saqib Bhatti more like this
1346826
registered interest false more like this
date less than 2021-07-14more like thismore than 2021-07-14
answering body
Department of Health and Social Care remove filter
answering dept id 17 more like this
answering dept short name Health and Social Care more like this
answering dept sort name Health and Social Care more like this
hansard heading Medicines and Medical Devices Safety Independent Review remove filter
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 report of the Independent Medicines and Medical Devices Safety Review entitled First Do No Harm published in July 2020, what recent steps he has taken to progress implementation of the recommendation for a redress agency for people harmed by medicines and medical devices. more like this
tabling member constituency Meriden more like this
tabling member printed
Saqib Bhatti more like this
uin 33367 more like this
answer
answer
is ministerial correction false more like this
date of answer less than 2021-07-26more like thismore than 2021-07-26
answer text <p>The Government response to the Report of the Independent Medicines and Medical Devices Safety Review was published on 21 July. The Government stated that it did not accept recommendation three to establish a redress agency as set out in the report. The Government and others have previously established redress schemes without the need for an additional agency.</p> more like this
answering member constituency Mid Bedfordshire more like this
answering member printed Ms Nadine Dorries more like this
question first answered
less than 2021-07-26T12:20:18.367Zmore like thismore than 2021-07-26T12:20:18.367Z
answering member
1481
label Biography information for Ms Nadine Dorries more like this
tabling member
4818
label Biography information for Saqib Bhatti more like this