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Pharmacovigilance system requirements
Guide to licensing procedure and other restrictions for export of controlled dual-use items, software and technology, goods for torture and radioactive sources.
The epidemiology, symptoms, diagnosis and management of Nipah virus infections.
Use a separate statement of objection form for each Japanese GI product name you object to.
Make sure that domains that do not send email cannot be used for spoofing.
The Intellectual Property Office offers different methods of accelerating the processing of your patent application.
Information about the EU Regulations and their implementation in Northern Ireland
How to apply for an exemption to use a restricted substance to manufacture electrical and electronic equipment.
Check the tariff classification for dried buffalo ears and dried beef meat scraped off from the throat, for use as animal feed.
An overview of the process including submitting or fast tracking an application, naming your medicine and paying fees.
Information to help you protect, manage and enforce your intellectual property (IP) rights in Colombia.
This toolkit is for Innovation Passport holders following the Innovative Licensing and Access Pathway (ILAP) and provides activities to support the design and development of medicines.
Check the regulations on aircraft parts imported with a certificate of airworthiness.
Guidance for manufacturers and distributors of premixtures and feedingstuffs containing veterinary medicines or specified feed additives.
Find out if you need an Academic Technology Approval Scheme (ATAS) certificate to study in the UK.
Look up a trade mark to see if something identical or similar to your brand is already registered.
Find out about the changes if you are exporting personal protective equipment (PPE) during the coronavirus pandemic.
Check the tariff classification for peptide nisin standardised with sodium chloride
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.
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
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