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What you need to do to supply authorised medicines from Great Britain to Northern Ireland.
Reported problems with the supply of an animal medicine and the date when the issue is expected to be resolved.
Apply for an authorisation to manufacture authorised veterinary medicines and medicines marketed under the Exemptions for Small Pet Animals.
The actions to take for sourcing medicines in different circumstances.
Guidance on prescribing or supplying veterinary medicines including requirements for registration and inspection of premises.
Check which Authorised Economic Operator status you could apply for and their benefits if your business has role in the international supply chain.
Guidance for manufacturers and distributors of premixtures and feedingstuffs containing veterinary medicines or specified feed additives.
Guidance for prescribing vets on the use of the cascade.
Guidance providing practical information for placing construction products on the GB market.
A wholesale dealer in Great Britain may import Qualified Person certified medicines from the European Economic Area if certain checks are made by the ‘Responsible Person (import)’
Guidance for UK wholesalers and manufacturers on how to import human medicines including unlicensed medicines, how to apply for a licence and how much it costs.
What you need to do to supply investigational medicinal products (IMPs) from Great Britain to Northern Ireland.
Applications closed open for the 2018 Nuclear Decommissioning Authority (NDA) Estate Supply Chain Awards on 5 September.
Decide which activities are business or non-business for VAT purposes if you're a local authority or other public body.
As a vet or pharmacist, you must follow legal requirements when working with controlled drugs in veterinary medicine.
How to apply for approval for a suitably qualified person (SQP) retailer premises to sell or supply animal medicines.
Importing investigational medicinal products for use in clinical trials
If the UKCA marking applies to products you manufacture or supply, you will have specific obligations and responsibilities for compliance, depending on your role.
The approach the MHRA intends to take for products approved or pending in decentralised procedure (DCP) or mutual recognition procedures (MRP).
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