1-20 of 359 results for subject:"Veterinary Medicines Directorate"
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To ask the Secretary of State for Environment, Food and Rural Affairs, when were businesses notified of the reclassification of valerian root by the Veterinary Medicines Directorate.
To ask the Secretary of State for Environment, Food and Rural Affairs, when were businesses notified of the reclassification of valerian root by the Veterinary Medicines Directorate.
The Veterinary Medicines Directorate considers valerian root to be medicinal by function, above a certain strength, in line with the Veterinary Medicines Regulations 2013 (as amended) definition of a veterinary medicine. The medicinal status applied to valerian root was established in 1992 and the substance has not been reclassified.
To ask His Majesty's Government further to the written answer by Baroness Hayman of Ullock on 11 February 2025 (HL4483), what research activities the Veterinary Medicines Directorate has conducted to provide further evidence on the environmental impacts of fipronil and imidacloprid in pet flea and tick treatments.
To ask His Majesty's Government further to the written answer by Baroness Hayman of Ullock on 11 February 2025 (HL4483), what research activities the Veterinary Medicines Directorate has conducted to provide further evidence on the environmental impacts of fipronil and imidacloprid in pet flea and tick treatments.
The Veterinary Medicines Directorate (VMD) has undertaken a number of research activities to strengthen the evidence base on how fipronil and imidacloprid from topical flea and tick treatments may enter and affect the environment. Recently published VMD‑funded studies (2024–25) demonstrated that spot‑on flea and tick products can contribute to environmental residues through wastewater pathways and when treated dogs swim, providing the first UK‑specific exposure data for these routes. To build on this, the VMD has commissioned further work to address key evidence gaps identified at the 2025 Pharmaceuticals in the Environment (PiE) stakeholder workshop, including exposure modelling to better quantify environmental inputs and research on how pet owner behaviours influence environmental outcomes.
In 2025 the VMD launched a national pet owner survey, which closed in January 2026, to provide an indicative baseline of current pet owner product use and disposal practices. Additional behavioural research through the University of Plymouth will complement these findings.
These research outputs will support targeted communications, stewardship initiatives and future regulatory decision‑making.
To ask His Majesty's Government, further to the Written Answer by Baroness Hayman of Ullock on 5 February (HL14038), why the potential risks of chronic exposure to users and children is not listed in the Veterinary Medicines Directorate product information database of authorised products.
To ask His Majesty's Government, further to the Written Answer by Baroness Hayman of Ullock on 5 February (HL14038), why the potential risks of chronic exposure to users and children is not listed in the Veterinary Medicines Directorate product information database of authorised products.
When conducting a user risk assessment, before a veterinary medicine is authorised, both the hazards and the likely exposures to humans, including the children in a household, are considered. Data from both acute and chronic toxicology studies using animal models are used to identify the possible negative reactions that may be seen in humans if exposed. Several exposure scenarios are considered, including reasonable worst-case scenarios, leading to a conservative estimate of the actual risks to those that may come into contact with a veterinary medicine. A hazard may be identified, but if the exposure to the medicines is likely to be low, then this leads to minimal risk to the person. If risks are identified, they are listed on the product information database, alongside advice on how to minimise those risks. VMD collects data on adverse reactions reported to them and to pharmaceutical companies, once a product is on the market, and can update the risk profile and user warnings where these data indicate a concern.
To ask the Secretary of State for Environment, Food and Rural Affairs, how much the Veterinary Medicines Directorate has spent on translation and interpretation services in each of the last five years.
To ask the Secretary of State for Environment, Food and Rural Affairs, how much the Veterinary Medicines Directorate has spent on translation and interpretation services in each of the last five years.
The Veterinary Medicines Directorate’s spending on translation and interpretation service was funded by the Bill and Melinda Gates Foundation. The below table shows the total cost over the past five years.
This information is in the public domain.
Financial Year | Total VMD Cost | Function – All funded by a BMGF project. |
20/21 | Nil | Nil |
21/22 | £1,913.51 | Online Translation subscription and workshop interpretation from English to French and vice versa. |
22/23 | £19,257.00 | Online Translation subscription and interpretation service at three regional conferences in Sub-Saharan Africa from English to French and vice versa. |
23/24 | £212.54 | Online Translation subscription |
24/25 | £141.19 | Online Translation subscription |
Total | £21,524.24 |
|
To ask the Secretary of State for Environment, Food and Rural Affairs, how much the Veterinary Medicines Directorate has spent on equipment to enable staff to work from home in each of the last three years.
To ask the Secretary of State for Environment, Food and Rural Affairs, how much the Veterinary Medicines Directorate has spent on equipment to enable staff to work from home in each of the last three years.
The Veterinary Medicines Directorate’s (VMD’s) spend on equipment to enable staff to work from home in each of the last three years is:
Year | Total |
|
FY2022/23 | £10,579.77 |
|
FY2023/24 | £6,248.34 |
|
FY2024/25 | £3,235.72 |
|
The VMD is unable to differentiate between costs that are associated with the provision of equipment for use at home relating to a workplace adjustment, and formal working contracts versus any costs associated with hybrid working arrangements. Obtaining this information could only be achieved at a disproportionate cost.
The VMD, in common with other directorates and Government departments, has agreed that 60% minimum office attendance for most staff continues to be the best balance of working for the Civil Service.
To ask the Secretary of State for Environment, Food and Rural Affairs, what steps his Department is taking to support the Veterinary Medicines Directorate’s five-year strategy to improve the (a) availability and (b) continuity of supply of sheep vaccines.
To ask the Secretary of State for Environment, Food and Rural Affairs, what steps his Department is taking to support the Veterinary Medicines Directorate’s five-year strategy to improve the (a) availability and (b) continuity of supply of sheep vaccines.
Defra is aware of the concerns regarding the availability and continuity of supply of vaccines for sheep and other animal species. The Veterinary Medicines Directorate, an agency of Defra, has held several meetings convening stakeholders from across government, the pharmaceutical industry and wider animal health sector to discuss the barriers and potential solutions to improving vaccine availability and innovation. These discussions highlighted the complex multifactorial nature of the problem and the need to champion a collaborative, cross-sector approach moving forwards. The intention is to publish a statement of intent outlining a strategic framework for such an approach in the near future.
To ask the Secretary of State for Environment, Food and Rural Affairs, whether he has made an assessment on the effectiveness of the Veterinary Medicines Directorate since it removed the ability to submit reports online.
To ask the Secretary of State for Environment, Food and Rural Affairs, whether he has made an assessment on the effectiveness of the Veterinary Medicines Directorate since it removed the ability to submit reports online.
The provision of a Web reporting route for suspected adverse event cases to the Veterinary Medicines Directorate (VMD) is not mandatory and, therefore, its suspension does not affect the VMD’s approach to assessment.
Reporting of adverse events continues directly through the adverse.events@vmd.gov.uk mailbox for non-authorised veterinary medicinal products or for authorised products should the reporter be unable to report directly to the Marketing Authorisation Holder.
To ask the Secretary of State for Environment, Food and Rural Affairs, for what purposes the Veterinary Medicines Directorate has used artificial intelligence in the last 12 months.
To ask the Secretary of State for Environment, Food and Rural Affairs, for what purposes the Veterinary Medicines Directorate has used artificial intelligence in the last 12 months.
Artificial Intelligence (AI) is at the heart of the Government’s plan to kickstart an era of economic growth, transform how we deliver public services, and boost living standards for working people across the country.
The Veterinary Medicines Directorate (VMD) has not used AI within any business processes to aid decision making regarding the quality, safety or efficacy of the lifecycle of veterinary medicines within the last 12 months.
The VMD submitted a nil return to Cabinet Office regarding the Algorithmic Transparency Recording Standard (ATRS) on 30 August 2024.
The VMD can draw on a range of resources, published on GOV.UK, to inform AI usage. For example, the Generative AI Framework, the Ethics, Transparency and Accountability Framework, the Data Ethics Framework, the AI Opportunities Action Plan and the ATRS.
The Directorate also has access to the Government Digital Service, part of the Department for Science, Innovation & Technology, for expert advice.
To ask the Secretary of State for Environment, Food and Rural Affairs, if he will make an assessment of the adequacy of the number of food samples tested for lead contamination per year by the Veterinary Medicines Directorate.
To ask the Secretary of State for Environment, Food and Rural Affairs, if he will make an assessment of the adequacy of the number of food samples tested for lead contamination per year by the Veterinary Medicines Directorate.
The levels of lead testing in the United Kingdom are determined in accordance with legislative requirements which provide food safety assurances to both domestic consumers as well as export markets. Sampling levels are reviewed by the Veterinary Medicines Directorate (VMD) each year to ensure that they are proportionate to livestock production; of note, the VMD has effectively tripled annual lead testing for sheep and bovine animals from 2024 to provide further guarantees on safety of these foodstuffs. The results of said testing are published by VMD on a quarterly basis and can be found on the VMD’s GOV.UK webpage here.
Motion to consider. Agreed to on question.
Motion to consider. Agreed to on question.
Lords motion to consider. Agreed to on question.
Lords motion to consider. Agreed to on question.
My Lords, these regulations were laid in draft before the House on 4 March. They seek to amend the legislative regime for veterinary medicines set out in the Veterinary Medicines Regulations 2013 in respect of Great Britain. The amendments will ensure that the law is fit for purpose to protect...
My Lords, these regulations were laid in draft before the House on 4 March. They seek to amend the legislative regime for veterinary medicines set out in the Veterinary Medicines Regulations 2013 in respect of Great Britain. The amendments will ensure that the law is fit for purpose to protect...
My Lords, first, I say a warm welcome to these new regulations, which are in general welcomed by the veterinary pharmaceutical industry and, I should also say, by the veterinary profession in general, because they are the first major revision of veterinary medicine regulations since 2013. Given the pace of...
My Lords, first, I say a warm welcome to these new regulations, which are in general welcomed by the veterinary pharmaceutical industry and, I should also say, by the veterinary profession in general, because they are the first major revision of veterinary medicine regulations since 2013. Given the pace of...