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Data, Freedom of Information releases and corporate reports
The Foreign, Commonwealth & Development Office (FCDO) provides lists of English-speaking lawyers abroad to help British nationals find the legal support they need.
A wholesale dealer in Great Britain may import Qualified Person certified medicines from the European Economic Area if certain checks are made by the ‘Responsible Person (import)’
Details of General Licences issued by OFSI
Find registered patents, patent applications and pending patents
What you need to know before you can place a medical device on the Great Britain market with a UKCA mark.
Apply for changes to your marketing authorisation, including minor variations type IA and IB, major variations type II and extensions.
Apply to manufacture Extemporaneous preparations, Autogenous vaccines, authorisations for Equine Stem Cell Centre (ESCCA) or Non-Food Animal Blood Bank (NFABBA).
Get information on teacher training courses, funding, pay scales and how to make a great application
Guidance on the Specific Batch Control (SBC) scheme for release of product on to the UK market.
Apply for an authorisation to manufacture authorised veterinary medicines and medicines marketed under the Exemptions for Small Pet Animals.
Pharmacovigilance system requirements
Guidance on the decentralised and mutual recognition reliance procedure (MRDCRP) for marketing authorisation applications including information on how to apply.
Information about the EU Regulations and their implementation in Northern Ireland
Find out about the changes if you are exporting personal protective equipment (PPE) during the coronavirus pandemic.
Applications received to amend the specification of a patent under sections 27 and 75 before the court and the Office.
Check the regulations on aircraft parts imported with a certificate of airworthiness.
Use this form to file a translation in connection with a European patent or a European patent application
Export controls applying to Weapons of Mass Destruction (WMD) related activities - transfer of technology and provision of technical support
An overview of the process including submitting or fast tracking an application, naming your medicine and paying fees.
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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