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Register to vote Register by 18 June to vote in the General Election on 4 July.
Information about new applications, post-licensing, advertising, product information and fees.
Directory of current ICH Guidelines which have been implemented by the Medicines and Healthcare products Regulatory Agency.
Guidance for industry on flexible approaches we are taking on good distribution practices.
Apply for an import certificate to import a medicinal product into the UK for veterinary use.
Advice and guidance on the health needs of migrant patients for healthcare practitioners.
You must get permission to export certain drugs and medicines.
How to comply with the exemption from the Veterinary Medicines Regulations that allow certain animal medicines to be sold without a marketing authorisation.
Apply for a promising innovative medicine (PIM) designation or scientific opinion for your medicine from MHRA.
How to apply for an authorisation to manufacture authorised veterinary medicines or medicines marketed under the Exemptions for small pet animals.
Dawa Limited has informed the MHRA that specified batches listed in this notification have been packed with an outdated Patient Information Leaflet (PIL).
Guidance for UK wholesalers and manufacturers on how to import human medicines including unlicensed medicines, how to apply for a licence and how much it costs.
Information on good laboratory, manufacturing and distribution practice, good pharmacovigilance practice (GPvP), out-of-specification investigations, inspection metrics and fees.
You must include the appropriate legal basis for your application when you apply to MHRA for a marketing authorisation.
Actions that trial sponsors should consider to build resilience into clinical trial design
What you need to know before you can place a medical device on the Great Britain market with a UKCA mark.
Guidance for the veterinary pharmaceutical industry on the production of mock-ups for assessment.
What you need to do to supply authorised medicines from Great Britain to Northern Ireland.
Apply for changes to your marketing authorisation, including minor variations type IA and IB, major variations type II and extensions.
How marketing authorisation holders should inform MHRA of a signal or an ADR to a medicine.
Information on carrying medicine containing controlled drugs for individual travellers entering or leaving the UK.
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