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How to show MHRA you're meeting good clinical practice (GCP) standards and what to expect from an inspection.
The official report of all Parliamentary debates. Find Members, their contributions, debates, petitions and divisions from published Hansard reports dating back over 200 years.
Apply for a certificate to use a CITES-listed specimen for commercial purposes.
This series brings together all documents relating to Research
Get help to classify ceramic articles for import and export.
Check the tariff classification for articles and equipment for general physical exercise and other sports or outdoor games.
Check the tariff classification for four-wheeled vehicles powered by an electric motor fitted with a hydraulic lifting device and telescopic jib.
Change your protocol, update your authorisation, report safety issues, submit safety updates and complete your end-of-trial study report.
How to register your medical devices with the Medicines and Healthcare products Regulatory Agency (MHRA) for the markets in Great Britain and Northern Ireland
Volume 38 of the non-technical summaries granted under the Animals (Scientific Procedures) Act 1986 during 2013.
Submission dates and how the submissions using the EC decision reliance procedure work.
How to make sure that your products are properly checked for conformity and your technical documents are managed correctly.
Get help to classify textiles and which headings and codes to use.
This is the Hub for all the Veterinary Medicines Directorate's communications on current and future regulatory changes.
How to apply to import, export or re-export endangered animal and plant species on the Convention on International Trade in Endangered Species of Wild Fauna and Flora (CITES) list.
Designated land, sea and air ports for trading or moving CITES-listed endangered animals, plants, or their parts and derivatives.
The controls that apply if you transport waste out of or into England.
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