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Apply for an import certificate to import a medicinal product into the UK for veterinary use.
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.
Links to EU guidance, as it stood immediately before end of transition period.
Guidance for industry on flexible approaches to regulation we are taking during the COVID-19 outbreak.
This guidance provides information on comparator products used in studies supporting abridged marketing authorisation applications
How we evaluated pre-exposure prophylactic (preventative) treatments for COVID-19.
Pharmacy, prescription-only (POM), and general sale list (GSL) medicines: apply to move your medicine to a different classification.
Comply with good pharmacovigilance practice and prepare for an inspection.
How to submit your periodic safety update report report (PSUR) or periodic benefit risk evaluation report (PBRER)
How to package medicines for sale and what information you must provide to consumers and healthcare professionals.
How to comply with the requirements on promoting medicines to the public and to prescribers and suppliers of medicines.
Advice and guidance on the health needs of migrant patients for healthcare practitioners.
There are changes to the legislation of Reference Medicinal Products (RMPs) used to support abridged marketing authorisation applications
Information and guidance on a range of medical devices for users and patients.
Information about how to register your homeopathic medicinal product through the Simplified Homeopathic Registration Scheme or the UK Homeopathic National Rules Scheme
How veterinary medicines can be advertised.
What you need to know before you can place a medical device on the Great Britain market with a UKCA mark.
Apply for an authorisation to manufacture authorised veterinary medicines and medicines marketed under the Exemptions for Small Pet Animals.
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