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Grievances and disciplinary action at work can be solved by informal discussions, formal procedures, mediation, conciliation or arbitration.
Applications received to amend the specification of a patent under sections 27 and 75 before the court and the Office.
If you are found guilty of a crime, your sentence will depend on a number of factors, including the type, seriousness and circumstances of the crime.
Check what side effects people have reported when they've taken a medicine.
How we evaluated pre-exposure prophylactic (preventative) treatments for COVID-19.
Check the tariff classification for animal beds.
Legal terms for veterinary medicines, marketing of non-medicinal products including medicinal words and phrases, how to complain.
Helping public health practitioners conducting evaluations – using economic evaluation to identify the value gained from an intervention.
How to tax a beneficial loan arrangement for a director or employee.
Check the tariff classification for vitamin gummies.
Check the tariff classification for a defined daily dose of active substances.
A collection of guidance about how to protect, manage and enforce copyright. Copyright protects original literary, dramatic, musical and artistic works.
The combined views of experts from academia, industry and government captured at roundtables about a range of topics can be found in the summary meeting notes below.
Documents, certificates, letters and notes available at the British consulate in Argentina.
If you're advertising or marketing, including direct marketing, you must be accurate and honest and follow the advertising codes of practice
We give statutory advice to ministers on the risks to human health and the environment from the release of genetically modified organisms (GMOs). ACRE is an advisory non-departmental public body, sponsored by the Department for Environment, Food & Rural Affairs...
How to comply with the requirements on promoting medicines to the public and to prescribers and suppliers of medicines.
The Accelerated Access Review aims to speed up access to innovative drugs, devices and diagnostics for NHS patients.
Explainer for the pharmaceutical industry on Renewal requirements mitigations to bridge the gap between the implementation of the EU Regulation on veterinary medicines and the revised Veterinary Medicines Regulations as they have an effect in Great Britain (GB VMR).
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