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Information on which products to list when completing an adverse event report for an animal medicine or a product which an animal has been exposed to.
What happens after you have submitted the online report of an adverse event to an animal medicine.
If you're a collective investment vehicle fund manager or authorised to act on behalf of a fund manager, find out how to register for the Secure Data Exchange Service to send annual exemption election reports.
Getting involved in fisheries management can seem complicated. Many stakeholders are unsure where to begin or do not feel confident about the process. The Regional Fisheries Groups (RFGs) have provided clear, practical guide…
If you import goods into Northern Ireland from outside the EU for onward supply to the EU, find out about claiming Onward Supply Relief.
What you must do if you wish to use the Security Industry Authority's Licence Management service.
For public sector organisations, DVS provides valuations and property advice.
How we support HM Revenue and Customs, the Valuation Office Agency and the Home Office to learn from complaints and work with them to improve their service.
This note is part of the statutory guidance under s215 of the HRA 2008 (from 1 April 2024)
If pharmacies wish to ‘pack down’ larger packs of a medicinal product, they need to follow these instructions
Guidance on following the Data Protection Act rules for driving examiners who carry out instructor tests and checks.
Information and examples and how to calculate specified amount.
Full results of the second stage of environmental checks carried out on the soil around the Grenfell Tower site between May 2020 and April 2021.
What needs to be done to manage flood risk and adapt to rising sea levels in Greenwich, one of 23 policy units in Thames Estuary 2100 (TE2100).
Keep up-to-date with regular and ongoing events of the profession and beyond.
Information on business continuity procedures for Goods Vehicle Movement Service.
Requirements for transport of the veterinary medicinal products .
Notification to the VMD if they have a reason to suspect, or know of, a threat to the continued supply of a veterinary medicine.
Requirements for a self-inspection programme.
Guidance on Pharmacovigilance reporting.
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