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Departments, agencies and public bodies
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Annual statistics about pensioners’ incomes
Guidance for the veterinary pharmaceutical industry on the production of mock-ups for assessment.
This collection brings together all documents relating to housing supply: indicators of new supply statistics.
Submission dates and how the submissions using the EC decision reliance procedure work.
Upper Tribunal Tax and Chancery decision of Judge Thomas Scott and Judge Ashley Greenbank on 29 April 2024
Guidance for the pharmaceutical industry on applying for a marketing authorisation for parallel import (MAPI).
The Foreign and Commonwealth Development Office's file review and release process.
Guidance for the pharmaceutical industry on how to apply to vary a veterinary Marketing Authorisation (MA) or Homeopathic Remedy.
Guidance for manufacturers, importers and distributors.
Use form ALVS1 if the Automatic Licence Verification System cannot process an automatic release on CHIEF or the Customs Declaration Service.
Income Tax deducted from pay by industry shows the industry distribution of PAYE (Pay As You Earn) tax deducted from pay by tax year.
How to apply for, update and cancel licences for the manufacture, import and wholesale of human and veterinary medicines.
Guide to licensing procedure and other restrictions for export of controlled dual-use items, software and technology, goods for torture and radioactive sources.
Licences to release non-native species into the wild
Check if your import, export or re-export needs a permit or certificate under the Convention on International Trade in Endangered Species of Wild Fauna and Flora (CITES).
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.
News and information about updates for each inspection data summary report (IDSR) release, including any new functionality, features and bug fixes.
This register details any personally identifiable or de-personalised data releases made by the Office for Data Release.
How to notify the MHRA of your intention to carry out a clinical investigation for medical devices.
How to register your medical devices with the Medicines and Healthcare products Regulatory Agency (MHRA) for the markets in Great Britain and Northern Ireland
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