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Pharmacovigilance system requirements
How to apply for British citizenship if you're a British overseas citizen, protected person, subject, national or overseas territories citizen - who's eligible, fees and where to send your application.
Apply for changes to your marketing authorisation, including minor variations type IA and IB, major variations type II and extensions.
Make sure that domains that do not send email cannot be used for spoofing.
Marburg virus is a Filovirus which, along with Ebola virus, can cause a severe and often fatal viral haemorrhagic fever (VHF).
Information about the EU Regulations and their implementation in Northern Ireland
Use these EU country codes, VAT numbers and foreign language letters to complete an EC Sales List (ESL).
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.
Look up a trade mark to see if something identical or similar to your brand is already registered.
Check the tariff classification for chewing tobacco and snuff (nasal tobacco).
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.
Covering thalidomide, lenalidomide, and pomalidomide: temporary guidance for pregnancy prevention arrangements for patients taking them during COVID-19
Visit the UK as a Standard Visitor for tourism, business, study (courses up to 6 months), medical treatment and other activities. Find out whether you need a Standard Visitor visa, or can visit without a visa.
Check the tariff classification for flavour pods.
The requirements for packaging DNLEU
Development of a standard approach for AI and autonomy in networked multi-sensor systems in security and defence.
Find out what you'll need to get a legally binding decision on the commodity code to use when importing or exporting your goods.
Explainer on product information templates to be used by applicants and Marketing Authorisation Holders (MAHs) of veterinary medicines.
Explainer for the pharmaceutical industry on the implementation of the Veterinary Medicines Regulation relating to Pharmacovigilance.
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