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Guidance for the pharmaceutical industry on Marketing Authorisations for veterinary medicines.
Look up a trade mark to see if something identical or similar to your brand is already registered.
Information to help you protect, manage and enforce your intellectual property (IP) rights in China.
Use form C88 (status) as proof of authorisation to import or export for the country of destination.
Apply for an authorisation to manufacture authorised veterinary medicines and medicines marketed under the Exemptions for Small Pet Animals.
What you need to do to work and operate in the aviation industry.
Information to help you protect, manage and enforce your intellectual property (IP) rights in Colombia.
Apply for an import certificate to import a medicinal product into the UK for veterinary use.
Reclaim VAT you've paid on goods and services bought in the UK to use in your business if you’re registered as a business outside the UK.
Explainer for the pharmaceutical industry on the implementation of the Veterinary Medicines Regulation relating to Pharmacovigilance.
The UK Good Laboratory Practice Monitoring Authority (UK GLPMA) recognises that there are potential challenges COVID-19 will present to members of the GLP monitoring programme.
How to apply for an exemption to use a restricted substance to manufacture electrical and electronic equipment.
To help you protect, manage and enforce your intellectual property (IP) rights in Laos.
General announcements and latest decisions of the Certification Officer
Find out about applying for the Spirit Drinks Verification Scheme, how to submit brand information, fees and making sure your production process is compliant.
Information on how to gain a UK CoC for Engineering/Electro-Technical Officers or Engineering Watch Rating Certificate
Guidance for organisations involved in any aspect of the pharmaceutical lifecycle or GLP studies regulated by MHRA, covering the approval of paper documents when working from home
How to get fast-track approval of medical devices during COVID-19.
Guidance for industry on preparing responses to good laboratory practice (GLP) and good clinical practice (GCP) inspection reports.
If the UKCA marking applies to products you manufacture or supply, you will have specific obligations and responsibilities for compliance, depending on your role.
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