GHNHSFT - Redirect

Dear FOI Team,

I hope you are well. I am writing to request information under the Freedom of Information Act 2000 regarding your Trust’s radiology and billing IT systems. To assist with your response I have set out a short set of questions and response tables below, and attached the same tables as an Excel workbook, should that be easier to complete.

1. Please provide details of your current Radiology Information System (RIS) and Picture Archiving and Communication System (PACS).
System Current supplier & product Contract expiry (mm/yyyy) Current contract value (£, if held)
RIS
PACS

2. Please list any AI or clinical decision-support tools currently in live use within radiology, with the clinical application (if applicable) and supplier for each.
AI / decision-support tool Clinical application – if applicable (e.g. stroke / CT head) Supplier In use since (year)
[Tool 1]
[Tool 2]

3. Please list any AI-based tools used by your trust for each of the following parts of the radiology workflow.
Radiology workflow segment Definition AI tool used Supplier In use since (year)
Reporting and documentation Structured reporting templates and report generation (including AI report drafting) [Tool 1]
[Tool 2]
Ambient Voice Transcription (AVT) Voice-to-text dictation used to produce reports [Tool 1]
[Tool 2]
Back-office and operational Data analytics and intelligence, clinical coding and revenue, workforce management and rostering, and patient communication [Tool 1]
[Tool 2]
[Tool 3]

4. Please indicate your Trust’s adoption of the following data and interoperability standards, stating for each whether it is in production, actively implemented, planned, or not adopted, since when, and the platform or vendor used where applicable.
Standard Adoption status
(in production / actively implementing / planned / not adopted / other) Since (year) Platform / vendor (if any)
openEHR (open clinical data platform)
HL7 FHIR (incl. FHIR UK Core)
OMOP Common Data Model
Imaging interoperability – VNA
Imaging interoperability -DICOMweb
Imaging interoperability – IHE XDS-I

A response in any standard electronic format is welcome; an Excel version of the tables is attached should it be easier. If any part of this request would exceed the appropriate cost limit, I would be grateful for your advice under Section 16 on how it could be refined; I would be happy to receive the most recent single year in place of the full three-year period if that helps keep it within the limit. Where an exemption applies to any part, please indicate it and release any non-exempt elements. I look forward to your response.

Best,

Dear FOI team,
I hope you are well. I am writing under the Freedom of Information Act (2000) to request information on your trust’s radiology reporting arrangements and workforce.
Whilst I have included response tables below, I have also attached an Excel input sheet in case this is easier for you to complete. Unless otherwise specified, please provide figures for the last four financial years (i.e., 2022/23, 2023/24, 2024/25, and 2025/26), or the most recent year available.
1. Please list the external teleradiology / outsourced and insourced reporting providers your Trust has used, with the reporting volume and annual spend for each, by financial year.
Provider Model (outsourced / insourced) Financial year Studies reported (volume) Annual spend (£) Contract expiry (mm/yyyy)
Provider 1 2022/23
2023/24
2024/25
2025/26
Provider 2 2022/23
2023/24
2024/25
2025/26
2. For your diagnostic reporting, please indicate the split between studies reported and studies currently awaiting reporting (your backlog), as counts or as a percentage, with a total and, if possible, a breakdown by modality.
Modality Studies reported (no. or %) Awaiting reporting / backlog (no. or %)
TOTAL (all modalities)
CT
MRI
X-ray / plain film
Ultrasound
Nuclear medicine / PET
Other
3. Please state your current consultant radiologist workforce (WTE/FTE).
Consultant radiologist posts (WTE/FTE) Number
Funded / established posts
Vacant / unfilled posts
If any part of this request exceeds the appropriate cost limit, could you please advise me, under Section 16, on how it could be refined? I am happy to receive the most recent single year of data in place of all four financial years if that allows for costs to remain below the limit. Where an exemption applies to any part, please indicate it and release any non-exempt elements. I look forward to your response.

Kind regards,

Dear Gloucestershire Health and Care NHS Foundation Trust,

I am emailing to request the following information under the Freedom of Information Act 2000:

1. Number of surgical procedures cancelled or postponed since Jan 1st 2022 due to problems with surgical instruments, including: inadequate sterilisation, missing instruments, or contamination concerns.

2. Number of internal incident reports or safety concerns raised since Jan 1st 2022 from health practitioners referring to issues with surgical equipment or instruments.

Please break down the information by calendar year and hospitals in your trust.

If you need to clarify anything in my request, or if you feel my request is too broad or vague for you to provide a response within the statutory 20 days, please get in touch with me so I can clarify or refine my request.

Please get in touch with me via email at poplars-sailed.8k@icloud.com.
Thank you for your help.

Kind Regards,

We write in our capacity as solicitors specialising in medical negligence and patient safety issues and write in connection with matters arising from radiology reporting services provided to patients of your Trust. We make this request pursuant to the Freedom of Information Act 2000 (FOIA) and, where applicable, the Environmental Information Regulations 2004.
We respectfully draw the Trust’s attention to its statutory obligations under section 1(1) FOIA to confirm whether the requested information is held and, if so, to provide it to us. We ask that the Trust address each question individually and provide the information in a clear and organised format.
Notice regarding exemptions
Before setting out our questions, we make the following observations regarding commonly cited exemptions, which we respectfully submit do not apply to the requests below:
Section 12 (Cost Limit): Each question below is drafted to be specific, time-limited and focused. The information sought is operational data which ought to be capable of retrieval from existing records systems without undue burden. We respectfully invite the Trust, before claiming this exemption, to engage constructively with a narrowed or reformulated version of any question it considers disproportionate, in accordance with the ICO’s guidance on exceeding the cost limit.
Section 22 (Future Publication): We do not accept that the public interest in deferring disclosure of information relating to patient safety and clinical governance outweighs the immediate public interest in transparency. We request that the Trust not rely on this exemption in relation to information concerning serious incidents, audit results or complaint data.
Section 36 (Prejudice to Conduct of Public Affairs): Given the strong public interest in NHS transparency and patient safety accountability — recognised by the Information Commissioner and the Upper Tribunal — we submit that this exemption is unlikely to be engaged or, if engaged, that the public interest in disclosure substantially outweighs any prejudice. The qualified person must apply genuine and specific reasoning, not a generalised assertion.
Section 41 (Information Provided in Confidence): Where commercial contracts are in issue, we acknowledge that individual commercially sensitive clauses may properly be redacted. However, the existence of a contract, its general scope, KPIs, SLAs and patient safety provisions do not, in our submission, constitute information imparted in confidence in a manner actionable at law, particularly where those arrangements directly affect patient care. We invite the Trust to apply any redactions narrowly and to provide a schedule of redactions with reasons, rather than withholding entire documents.
We respectfully ask that, before declining to answer any question, the Trust considers whether it would be proportionate to reformulate, narrow or provide partial information, consistent with its duty to provide advice and assistance under section 16 FOIA.
Part A: Outsourcing arrangements
Please answer the following questions in relation to the six complete financial years ending 31 March 2026 (i.e. 2020/21 to 2025/26) unless otherwise stated.
A1. Identity of Outsourced Providers
Please provide a list identifying each external or outsourced radiology reporting provider engaged by the Trust during the relevant period, stating for each:
(a) the company name and registered address;
(b) the contract commencement and expiry or termination date; and
(c) the imaging modalities covered (for example, MRI, CT, plain film/X-ray, ultrasound, nuclear medicine, or other). Where a single provider covered multiple modalities under separate arrangements, please list each separately.
A2. Annual Expenditure on Outsourced Reporting
Please state the total actual expenditure incurred by the Trust on outsourced radiology reporting services for each of the six financial years specified above, expressed as an annual figure. Please confirm whether the figures provided are inclusive or exclusive of VAT.
A3. Volume Split: Outsourced versus In-House Reporting
Please provide, for each of the six financial years specified above, the total number of radiology reports generated and the proportion fulfilled by
(a) outsourced providers
(b) in-house NHS radiologists, expressed both as absolute numbers and as a percentage of total volume. Where data is held by modality type, please provide the breakdown accordingly.
PART B: GOVERNANCE AND QUALITY ASSURANCE
B1. Quality Assurance Policies
Please describe the quality assurance processes and standards applied by the Trust to radiology reports produced by outsourced providers, including any minimum reporting standards, turnaround time requirements, and escalation procedures. Please provide copies of any written policies, protocols or frameworks currently in force, or those in force at any time during the relevant period.
B2. Audit of Outsourced Reporting Accuracy
Please describe how the Trust audits or otherwise monitors the clinical accuracy and quality of reports produced by outsourced providers. Please provide copies of the findings, outcomes and recommendations of any such audits or quality reviews carried out during the relevant period, including any discrepancy rates identified.
B3. Registration and Professional Standards Requirements
Please confirm whether the Trust requires, as a contractual condition or as a matter of policy, that all radiologists engaged by outsourced providers hold:
(a) full registration with the General Medical Council (GMC) with a licence to practise; and/or
(b) Fellowship of the Royal College of Radiologists (FRCR) or equivalent qualification.
If different or lesser requirements are applied, please specify what standards are required and on what basis.
B4. Verification of Individual Radiologist Competency
Please describe the process by which the Trust verifies, at the time of contract award and on an ongoing basis, the qualifications, subspecialty expertise, revalidation status and clinical competency of the individual radiologists engaged by outsourced providers to report on Trust patients’ imaging. Please include details of any approved list, credential framework, or sign-off process used.
PART C: PATIENT SAFETY INCIDENTS AND REPORTING DISCREPANCIES
C1. Serious Incidents and Patient Safety Events
For each of the six financial years specified in Part A, please state the total number of Serious Incidents (SIs) or patient safety events recorded on the Trust’s incident reporting system (including Datix or any successor system) in which a radiology report was identified as a causative, contributory or associated factor, as follows:
(a) incidents involving a report produced by an outsourced provider; and
(b) incidents involving a report produced by an in-house radiologist.
For each category, please provide the year of occurrence, the incident category or classification applied, and the recorded outcome or learning.
C2. Peer Review Discrepancy Findings
Please confirm the number of significant or clinically relevant discrepancy findings identified through peer review, retrospective review, or multi-disciplinary team processes in relation to outsourced radiology reports, assessed by financial year and by provider name.
A ‘significant discrepancy’ should be understood to mean a finding that resulted in, or had the potential to result in a change in patient management.
Please also provide the equivalent figures for in-house reporting for comparison, where held.
C3. Contract Suspensions or Terminations on Patient Safety Grounds
Has the Trust at any time suspended the use of, or terminated a contract with, any outsourced radiology provider due to concerns about patient safety, clinical quality or reporting standards? If so, please provide for each instance:
(a) the name of the provider concerned;
(b) the date of suspension or termination;
(c) the stated reason(s); and
(d) any action taken to notify or review the care of patients whose imaging was reported by that provider during the period of concern.
Part D: Complaints
D1. Formal Complaints Relating to Radiology Reporting
Please state the total number of formal complaints received by the Trust under the NHS Complaints Procedure (as set out in the Local Authority Social Services and National Health Service Complaints (England) Regulations 2009) during each of the six financial years specified in Part A, which wholly or in part concerned radiology reporting, as to:
(a) complaints relating to reports produced by outsourced providers; and
(b) complaints relating to reports produced by in-house radiologists.
Please also confirm the number of those complaints that were upheld or partially upheld.
Part E: Clinical negligence claims and litigation
E1. Claims Involving Radiology Reporting
Please state the total number of clinical negligence claims notified to the Trust (whether under the Clinical Negligence Scheme for Trusts, NHS Resolution, or otherwise) during the six financial years specified in Part A, in which a radiology report was identified as a causative or contributory factor, as to:
(a) claims involving a report produced by an outsourced provider; and
(b) claims involving a report produced by an in-house radiologist.
Please note that we do not seek details of individual claims or any information from which a living individual could be identified.
E2. Value of Settled Claims
Please state the total quantum of damages and costs paid in respect of settled clinical negligence claims during the six financial years specified in Part A, where
(a) outsourced radiology reporting and
(b) in-house radiology reporting was identified as a causative or contributory factor.
Where the Trust does not hold this information, please indicate whether it is held by NHS Resolution and provide signposting accordingly.
E3. Referring Clinical Specialties in Outsourced Radiology Claims
In respect of clinical negligence claims involving outsourced radiology as a causative or contributory factor (as identified in question E1(a) above), please identify the clinical specialties that were the primary referring specialty, ranked in order of frequency. This information is sought in aggregate and anonymised form only.
Part F: Clinical integration and communication protocols
F1. Access to Prior Imaging and Clinical Information
Please describe the protocols and systems in place to ensure that outsourced radiologists, at the time of reporting, have access to:
(a) prior and comparator imaging held by the Trust or available via national image-sharing infrastructure;
(b) relevant clinical history and indication for the examination; and
(c) electronic patient records or relevant clinical documentation. Please provide copies of any written protocols or guidance currently in force.
F2. Communication of Urgent and Critical Findings
Please describe the Trust’s policy and procedure for the communication of urgent or critical imaging findings from outsourced reporting providers to the responsible clinical team, including:
(a) the Trust’s target timeframe for communication of a critical result;
(b) the actual recorded average or median timeframe for such communication during the relevant period, where data is held; and
(c) the escalation pathway if communication is not acknowledged within the target timeframe.
F3. Clinician Query and Clarification Process
Please describe the process available to a referring clinician who wishes to query, seek clarification on, or formally dispute the content of a report produced by an outsourced radiologist. Please specify any timeframe within which the outsourced provider is required to respond, and how such queries are documented.
Part G: Oversight, contractual standards and regulatory findings
G1. Key Performance Indicators and Service Level Agreements
Please provide copies of the Key Performance Indicators (KPIs) and Service Level Agreement (SLA) provisions contained within written contracts between the Trust and each outsourced radiology provider during the relevant period.
We acknowledge that certain commercially sensitive pricing provisions may be appropriately redacted; however, we request that KPIs, quality standards, discrepancy thresholds, turnaround times and patient safety provisions be disclosed in full. We invite the Trust to provide a schedule of any redactions made, with brief reasons.
G2. NHS Resolution and Regulatory Recommendations
Has NHS Resolution, the Care Quality Commission, NHS England, the Royal College of Radiologists, or any other regulatory or advisory body made any formal recommendations, findings, risk notices or improvement notices in relation to the Trust’s use of outsourced radiology reporting at any time during the relevant period? If so, please provide details including the date, the body concerned, the nature of any findings, and the Trust’s response or actions taken.
G3. Named Clinical and Managerial Responsibility
Please provide the job titles (but not the personal names) of the individual(s) who hold named clinical and managerial responsibility within the Trust for:
(a) oversight of the quality and safety of outsourced radiology reporting; and
(b) contract management and performance monitoring of outsourced radiology providers.
G4. Policies Governing Reporting Standards
Please provide copies of any policies, frameworks or standard operating procedures in place to ensure that outsourced radiology reporting is carried out to the required clinical and professional standard, including any minimum competency requirements, escalation policies, and processes for addressing identified underperformance.
G5. Participation in MDT and Discrepancy Meetings
Are outsourced radiologists required or invited to participate in multi-disciplinary team (MDT) meetings, radiology discrepancy meetings, morbidity and mortality meetings, or internal clinical investigations involving their reports?
Please describe any such arrangements and the policy basis for them.
G6. Process for Addressing Identified Errors
Where a clinically significant discrepancy or error is identified in a report produced by an outsourced radiology provider, please describe:
(a) the process by which the Trust notifies the outsourced provider of the finding;
(b) the process for reviewing whether other patients reported by the same radiologist may be affected;
(c) any duty of candour obligations engaged and how they are discharged; and
(d) the mechanism for feeding findings back into the quality assurance framework.
Compliance and response
We request that the Trust acknowledges receipt of this request promptly and provides its response within the statutory period of 20 working days from the date of receipt, in accordance with section 10 FOIA.
If the Trust considers that any question requires clarification before it can be answered, we respectfully ask that it contacts us at the earliest opportunity rather than allowing the statutory deadline to expire. We are available to discuss the scope of any request and to assist in narrowing or clarifying any question.
If the Trust intends to rely on any exemption in respect of any part of this request, we ask that it:
(a) identify clearly which question or part of a question is affected;
(b) specify the exemption(s) relied upon;
(c) where a qualified exemption is engaged, set out the public interest balancing exercise applied; and
(d) confirm whether the information is held.
A blanket or non-specific claim of exemption will not be regarded as compliant with the Trust’s obligations under FOIA.
Where information is provided in redacted form, please provide a schedule of redactions identifying what has been withheld and the statutory basis for doing so.
We draw attention to the right to request an internal review under section 50 FOIA and to refer any complaint to the Information Commissioner’s Office if the Trust fails to comply or relies on exemptions we consider improperly applied
Yours faithfully

Dear FOI Team,

I am writing to request recorded information under the Freedom of Information Act 2000 regarding the policies, procedures, and operational use of self administration of medication (SAM) within your maternity services.

Please provide the following information:

1. SAM policy documents Copies of any current or previous policies, guidelines, protocols, or standard operating procedures relating to self administration of medication in maternity services.
2. Implementation status Whether SAM is currently in use in any maternity settings within your Trust (e.g., antenatal wards, postnatal wards, day assessment units, birth centres).
o If yes, please specify which sites and clinical areas.
o If yes, is SAM optional or is it expected all patients do this with few exceptions (eg. Additional learning needs etc)
o If yes, please specify which medication SAM is used for – e.g. analgesia only
o If no, please state whether implementation is planned.
3. Eligibility criteria Any criteria, risk assessments, or decision making tools used to determine whether a maternity patient is eligible to self administer medication.
4. Training requirements Details of staff training, competencies, or mandatory modules relating to SAM in maternity services.
5. Audit or evaluation reports Any audits, evaluations, incident reports, or quality improvement reviews relating to SAM in maternity services from the past five years.
6. Patient information materials Copies of leaflets, consent forms, or information provided to maternity patients about SAM.
7. Digital systems Whether any electronic health record systems (e.g., BadgerNet) are used to record or support SAM processes, and if so, how this is documented.
8. Incidents Please give details about any incidents or adverse outcomes that have been related to SAM and what the level of harm and investigation process was.

Please provide the information electronically. I understand that under the FOI Act, I should receive a response within 20 working days. If any part of this request is unclear or would exceed the cost limit, please advise me as required under Section 16 of the Act so I may refine my request.

Kind regards,

Freedom of Information Request – Ref: FOI 161-2026 Thank you for your recent Freedom of...

Dear FOI team,

I am writing to you under the Freedom of Information Act 2000 to request the following information from your Trust. The questions relate to dermatology services your Trust commissions, including the use of teledermatology. Please could you provide me with answers to the following:

1. Teledermatology provision

Does your organisation currently use a teledermatology platform or system to support the delivery of dermatology services? If yes, please confirm whether this is used for any of the following purposes:
• Store-and-forward image review
• Advice and Guidance between primary and secondary care
• Remote consultation or virtual outpatient appointments
• Triage of urgent suspected skin cancer referrals

2. Technology platform
Please state the name of the teledermatology software platform or system currently in use. If more than one platform is in use, please list all and indicate the purpose of each.

3. Commissioning and funding arrangements

Is the teledermatology platform funded and procured directly by your organisation, or is it commissioned and funded by your ICB? If both apply, please clarify which platforms fall under each arrangement. Additionally, please indicate whether any of your teledermatology platforms are funded centrally, for example through research-supported or NHS England funding.

4. Contract details

Please state the start date, end date, and total contract value of the current teledermatology platform contract or contracts, where this information is not exempt from disclosure.

5. Procurement plans

Is there an active or planned procurement for a teledermatology platform currently under way or anticipated within the next 24 months? If yes, please provide details of the anticipated timeline.

6. Dermatology referral activity

For the most recent full financial year for which data is available, please provide:
• The total number of new referrals onto a dermatology Referral to Treatment (RTT) pathway received by your organisation
• The total number of urgent suspected cancer (two-week wait) referrals for skin cancer received by your organisation
• The total number of skin cancers diagnosed by your organisation

7. Key contacts

Please provide the name and contact details, or job title if personal details are not disclosable, of the following individuals within your organisation:
• The clinical lead for dermatology
• The operational or service lead responsible for dermatology services
• The individual responsible for digital or technology procurement within dermatology or the wider clinical directorate

Best wishes,

RE: Request under the Freedom of Information Act (2000)

Dear Information Team

This is an information request regarding compensation paid for maternity claims.

Please include the following information for the following years 2022/23, 2023/24, 2024/25 and 2025/26

• The total value of compensation claims paid in respect of maternity claims, please include a break down by:
o Claimant costs
o The Trust’s legal costs

• Total number of maternity compensation claims made, broken down by:
o Settled with admission of liability
o Settled without admission of liability
o Failed claims

• Total number of maternity claims currently open or in progress

• A breakdown of the reasons for maternity compensation claims and the number of cases that fell into each category.
o (for example Cerebral palsy and other brain injuries to the baby, stillbirth, neonatal death, other significant injury to the baby, maternal death, significant maternal injury, psychological injury etc)

• For each year please provide the largest maternity compensation claim including information on:
o Total damages paid
o The category of the maternal injury

If this is not possible to provide the information requested due to the information exceeding the cost of compliance limits identified in Section 12, please provide advice and assistance, under the Section 16 obligations of the Act, as to how I can refine my request.

If you have any queries please don’t hesitate to contact me via email or phone and I will be very happy to clarify what I am asking for.

I would prefer a response via email, but if not possible, I will gladly accept letters to the address below.

Please acknowledge this information request as soon as possible.

Kind regards,

Dear FOI Team,
Please treat this as a request for information under the Freedom of Information Act 2000.
I would be grateful if you could provide the following information regarding the Infection Prevention & Control (IPC) leadership and IPC nursing team at Gloucestershire Hospitals NHS Foundation Trust, covering:
• Gloucestershire Royal Hospital
• Cheltenham General Hospital
• Any associated services delivered by the Trust
1. IPC Leadership – Names, Roles, and Contact Details
Please provide the name, job title, and NHS email address (where publicly releasable) for the following positions:
• Director of Infection Prevention & Control (DIPC)
• Deputy DIPC
• Lead Nurse for Infection Prevention & Control
• IPC Matron / IPC Manager
• Infection Prevention & Control Doctor (IPCD)
• Any Consultant Microbiologists with designated IPC responsibility
2. IPC Nursing Team
For all IPC nursing staff employed by the Trust, please provide:
• Names
• Job titles and bandings
• NHS email addresses (where publicly releasable)
• The clinical areas or sites they cover
3. IPC Organisational Structure
Please provide:
• The most recent IPC organisational structure chart, including reporting lines
• Any documentation describing how IPC services are structured across the Trust
4. IPC Contact Information
Please provide:
• Any generic IPC team email addresses
• Any team telephone numbers used for clinical enquiries or staff contact
• Any site specific IPC contact details, if applicable
5. Additional IPC Documentation
If available, please provide:
• The most recent IPC Annual Report
• Any IPC governance documents or summaries produced within the last 12 months
If any part of this request is unclear or likely to exceed the appropriate cost limit, please let me know so I may refine it. I am happy to receive the information electronically.

Dear Sir/Madam,

I am writing for an FOI request regarding ECT treatments.

I would like to know the following:

1. What information (verbal, written) is given to patients prior to receiving ECT? Please provide a copy if a digital version exists, or otherwise list what information is provided regarding the procedure and potential side effects.
2. What is the level of consent and procedure prior to initiating ECT procedures? (e.g. is patient consent always required, or can it be overridden by a medical expert? Is there a standard procedure or a case-by-case basis?)

I look forward to your response in due time.

Kind regards,

Dear FOI Team,

I am writing to request information under the Freedom of Information Act regarding the use of wire free localisation devices within your organisation.

Please complete the attached table with the relevant information which you hold.

I understand the statutory deadline for FOI responses is 20 working days.I would be grateful to receive the information electronically as presented below.

Kind regards,
Ms. Ashleigh James (BSc, MBA)

These questions are in relation to the surgical treatment of Breast Cancer, using wire free localisation devices. These questions DO NOT relate to Biopsy clips or markers.

# Question Text Response Value (£) Quantity Date
1 Which department is currently responsible for the delivery of wire-free localisation devices? N/A N/A N/A
2 Who is the clinical lead for your organisations’ department? N/A N/A N/A
3 Is this department part of a wider clinical delivery network? i.e. West Midlands Cancer Alliance N/A N/A N/A
4 What system(s) are you currently using for wire-free localisation? N/A N/A N/A
5 Which supplier(s) was the current contract awarded to? N/A N/A N/A
6 When was the contract(s) awarded? N/A N/A N/A
7 How long is the contract(s) awarded for? Please include any extension options. N/A N/A N/A
8 Please provide the Contract Award Notice reference for the contract(s) listed in Question 5. N/A N/A N/A
9 What was the awarded value of the current contract(s)? N/A N/A N/A
10 Please confirm the procurement award route and market engagement undertaken prior to award, referencing any linked notices to Question 8. N/A N/A N/A
11 How many patients have been treated to date under the current contract(s)? N/A N/A N/A
12 How many systems are in operation as part of the current contract(s)? N/A N/A N/A
13 How many seeds or markers have been used as part of the current contract(s)? N/A N/A N/A
14 When is the current contract(s) due for retender? N/A N/A N/A
15 Who will lead on the new procurement process from a) Clinical Dept; b) Procurement N/A N/A N/A
16 Are there any other organisations who are named beneficiaries of this contract(s)? N/A N/A N/A

Dear Sir / Madam,

Under the Freedom of Information Act, please can you answer the following questions:

1. How much did your organisation spend on Sodium Hyaluronate eye drop formulations between the period of 01/01/2025 to 31/12/2025?

2. Between the period 01/01/2025 to 31/12/2025, which brand(s) of Sodium Hyaluronate eye drop formulations did you use?
To make your research easier, I have listed all commonly used brands which you can cross reference:

• Blink Intensive Tears
• Lacrifresh
• Artelac Rebalance
• Oxyal
• Xailin HA
• Optive Fusion
• Hyabak
• Hydramed
• Evolve HA
• Vismed Multi
• Clinitas Multi
• Eye Logic
• Euphrasia
• Biotrue
• Vismed Gel Multi
• Hysoothe
• Optrex Night Restore Gel
• Hy-Opti
• Hylo-Tear
• Murine Professional
• Hylo-Forte
• Hycosan Fresh
• Hylo Care
• Hycosan

3. How many units of each brand did you use?

Please respond to this email address.

Thanks and I look forward to hearing from you soon.

Dear NHS Trust

1. How many incidents of a retained foreign object post-procedure were logged by your Trust in the past three years? (2022/23, 2023/24, 2024/25)

1a) Please break down this information by year (as outlined above).

1b) If possible, please break down this information by retained object (including but not limited to the examples listed above).

NB Please interpret ‘retained foreign object post-procedure’ as objects accidentally left inside patients following surgical procedures – e.g. guide wires, mouth props, surgical instruments, needles, vaginal swabs, throat packs, clips etc.

Many thanks

Dear Trust FOI team,

Using the Freedom of Information Act 2000, I am writing to request data on the total number of instances of forced tranquilisation for the restraint of mental health patients in emergency departments in your trust each month, from the most recent month you have data for this, to as far back as records go.

All the best,

Dear NHS Trust

I am requesting this information under the Freedom of Information Act.

Could you please provide data in response to the following questions:

1. How many incidents of a retained foreign object post-procedure were logged by your Trust in the past three years? (2022/23, 2023/24, 2024/25)
NB Please interpret ‘retained foreign object post-procedure’ as objects accidentally left inside patients following surgical procedures – e.g. guide wires, mouth props, surgical instruments, needles, vaginal swabs, throat packs, clips etc.
1a) Please break down this information by year (as outlined above).
1b) If possible, please break down this information by retained object (including but not limited to the examples listed above).
2. How many claims have been made against the Trust in relation to retained foreign objects post-procedure in the past three years? (2022/23, 2023/24, 2024/25)
2a) Please break down this information by year (as outlined above).
3. What is the total sum paid out in claims made against the Trust in relation to retained foreign objects post-procedure in the past three years? (2022/23, 2023/24, 2024/25)
3a) Please break down this information by year (as outlined above).

3b) If possible, please provide the highest fee paid out in claims made against the Trust in relation to retained foreign objects post-procedure for each of the years outlined above.

Dear Sir or Madam

Please may I make a Freedom of Information request for the following information:

What percentage of babies have been born with thyroid conditions within the past twenty years spanning from December 2006 to March 2026?

Has there been an increase or a decrease in the percentage of babies that have been born with thyroid conditions within the last two decades?

Can you provide me with a statistic surrounding the current diagnosis rates of congenital thyroid conditions for new born babies as of March 2026 in comparison to December 2006?

Thank for very much for your time.

Yours Sincerely

FREEDOM OF INFORMATION REQUEST

Under the Freedom of Information Act, I would like to request the following information:

1. Has your NHS Trust purchased InSpace subacromial balloon spacer (Stryker) devices used for shoulder surgery for rotator cuff tears between 1st January 2013 to 1st January 2026? If so, how many devices?
2. How much money has your NHS Trust spent on Inspace subacromial balloon spacer (Stryker) devices purchased between 1st January 2013 to 1st January 2026?
3. How many Inspace subacromial balloon spacer (Stryker) devices have been used in surgeries / procedures conducted by your NHS Trust between 1st January 2013 to 1st January 2026?
4. How is the use of Inspace subacromial balloon spacer (Stryker) devices coded by your Trust?

I would like you to provide the information in an Excel spreadsheet or in a Microsoft Word table, via email at itm@warwick.ac.uk. Please contact me if you need me to clarify my request.

To whom it may concern,

I hope you are well. I am requesting the following information under the Freedom of Information Act.

• In the last year (March 2025 – February 2026), how many patients have come forward to be tested for prostate cancer through a Digital Rectal Exam (DRE)?
• Where data within the specified period is not available, please provide the last 12 months of available data
• If possible, please provide the age of patients coming forward

Many thanks for your time.

All the best,

Dear FOI team,
I am writing to request the following information under the Freedom of Information Act 2000.
Please provide the following recorded information relating to robotic-assisted surgical platforms currently available within your trust.
1. For each robotic-assisted surgical platform currently available within your trust, please provide:
• Manufacturer
• Model
• Date acquired or first brought into service
• Whether the platform is owned, leased, rented, or accessed via another arrangement
2. For each platform listed above, please specify the surgical specialties that use it.
3. For each platform, please provide the recorded source(s) of funding used to acquire or access it (e.g., trust capital, charitable funding, lease payments, donations, managed service agreements, third party funding arrangements).
4. Where charitable or philanthropic funding contributed to the acquisition or access arrangements for any platform, please provide:
• Name of the charitable organisation(s)
• Amount contributed by each
• Date the funding was received or allocated
5. Please provide the recorded annual cost of:
• Maintenance or servicing
• Consumables (if recorded separately)
• The funding source(s) used to meet these costs (e.g., trust budgets, charitable sources, managed service contract, warranty)
6. For each platform, please confirm whether it was acquired via an NHS Supply Chain framework or another procurement route, as recorded.

Freedom of Information Request – Ref: FOI 015-2026 Thank you for your recent Freedom of...

To NHS Trust:

Dear NHS Trust,

I am requesting this information under the Freedom of Information Act.

Could you please provide data in response to the following questions:

1. What are the longest A&E waiting times for NHS Trust patients for the past three calendar years? (Broken down by years 2023, 2024, 2025)
1a) If possible, please break down by age of patient.
1b) If possible, please break down by month.

2. What is the average A&E waiting time for NHS Trust patients for the past three calendar years? (Broken down by years 2023, 2024, 2025)
2a) If possible, please break down by age of patient.
2b) If possible, please break down by month.

3. How many NHS Trust patients have waited more than 24 hours to be admitted to hospital at A&E in the past three years? (Broken down by years 2023, 2024, 2025)
3a) If possible, please break down by age of patient.
3b) If possible, please break down by month.

If possible, can this be presented in PDF format please?

Many thanks,

Dear Freedom of Information Officer,

I am writing to make a request for information under the Freedom of Information Act 2000. I am seeking information regarding the use of 3D printing / additive manufacturing in orthopaedic trauma within your Trust.
If any part of my request exceeds the appropriate cost or time limits, I would be grateful if you could advise me on how to refine the request in accordance with Section 16 of the Act.

Please provide any recorded information you hold for the period 1 December 2015 – 1 December 2025, where applicable.

________________________________________
FOI Question 1 – Case Numbers
Please provide the total number of orthopaedic trauma cases in which 3D printing was used at your Trust between 1st December 2015 and 1st December 2025, along with an annual breakdown of these cases.
________________________________________
FOI Question 2 – Patient Demographics
For the cases identified above, please provide the number of patients by recorded gender (male, female, other) and the number of paediatric patients (
________________________________________
FOI Question 3 – Patient-Specific vs Generic 3D Printing
Please confirm whether your Trust currently uses 3D printing for:
a) patient-specific models, and
b) generic or reusable surgical tools or guides, and
c) implants (temporary or permanent)
________________________________________
FOI Question 4 – In-House Workflow
For any 3D printing performed in-house, please indicate which stages of the workflow are carried out internally (Imaging, Segmentation, Design, Manufacture, Quality Control, Operation), according to any recorded Standard Operating Procedures or workflow documentation.
________________________________________
FOI Question 5 – Imaging Modalities
Please list the imaging modalities used for 3D printing cases (CT, MRI, X-ray), including the approximate usage rate per case where available.
________________________________________

Please provide the information in electronic format where possible.
Thank you for your time and assistance. I look forward to your response within the statutory 20 working days.
If it is not possible to provide the information requested due to the information exceeding the cost of compliance limits identified in Section 12, please provide advice and assistance, under the Section 16 obligations of the Act, as to how I can refine my request.
If you can identify any ways that my request could be refined, I would be grateful for any further advice and assistance.
If you have any queries please don’t hesitate to contact me via email and I will be very happy to clarify what I am asking for and discuss the request, my details are outlined below.

Thank you for your time and I look forward to your response.