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As a vet or pharmacist, you must follow legal requirements when working with controlled drugs in veterinary medicine.
How to legally run a business that deals with the wholesale of animal medicines (veterinary medicinal products) and the WDA Register.
Uncontrolled release of liquid oxygen from a vacuum insulated evaporator (VIE).
Lists the main security measures appropriate for premises licensed to possess, supply or make controlled drugs or precursor chemicals.
Find out when it's possible to get zero-rated supplies on medical and research goods and services that have been funded by charities.
What you need to do to place a medical device on the Great Britain, Northern Ireland and European Union (EU) markets.
Find out which plastic packaging components are exempt or excluded from the tax, and if the packaging counts towards the 10-tonne threshold for registration.
The unit is a specialist in aerobiology, biocontainment and biosafety. The unit provides government departments and the commercial sector with expertise, advice and consultancy.
The T28 exemption allows pharmacies and similar places to denature controlled drugs to comply with Misuse of Drugs Regulations 2001.
How to package medicines for sale and what information you must provide to consumers and healthcare professionals.
Licence and registration application information for companies that deal in precursor chemicals.
Information on carrying medicine containing controlled drugs for individual travellers entering or leaving the UK.
Guidance on prescribing or supplying veterinary medicines including requirements for registration and inspection of premises.
Product Recall for Artemis & Alcudina White Double Door Bathroom Mirror Cabinets presenting a risk of injuries.
Legal terms for veterinary medicines, marketing of non-medicinal products including medicinal words and phrases, how to complain.
Comply with good manufacturing practice (GMP) and good distribution practice (GDP), and prepare for an inspection.
Information about the EU Regulations and their implementation in Northern Ireland
The requirements for 3D printed products will depend on whether they are classed as medical devices, personal protective equipment (PPE) or both.
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