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Get help to classify pharmaceutical products used to treat or prevent diseases or ailments (in humans or animals), including comparators used in clinical trials and placebos.
Submission dates and how the submissions using the EC decision reliance procedure work.
A bogus immigration lawyer with no licence to practise has been jailed for seven-and-a-half years for exploiting at least 19 victims for huge financial gain.
Find UK trade data from HMRC. Look up data about imports, exports, commodities and traders.
Use a separate statement of objection form for each Japanese GI product name you object to.
Information about when you need to submit substantial amendments to a clinical trial including changes to the trial sponsor or legal representative, Investigational medicinal product certification and importation.
Blogs where government organisations talk about their work and share information and ideas.
Advice and guidance on the health needs of migrant patients for healthcare practitioners.
Register as a manufacturer, importer or distributor of active substances.
Get help to classify organic chemicals that contain certain permitted additives or can be dissolved in water, for import and export.
How to prepare for implementation and compliance of the Safety Features Regulation.
How to apply for a clinical trial including eligibility, phases, model IMPDs, costs and how to make changes to your application.
Imposing safeguard measures for imports of certain steel products.
How to apply for marketing authorisation via this new procedure.
How to conform with the legal requirements for placing medical devices on the market.
Guidance for the pharmaceutical industry on how to apply to vary a veterinary Marketing Authorisation (MA) or Homeopathic Remedy.
Apply for an import certificate to import a medicinal product into the UK for veterinary use.
Check if you need a tuberculosis (TB) test to support your visa application and find an approved clinic in your country
Guidance for the pharmaceutical industry on Marketing Authorisations for veterinary medicines.
Guidance for veterinary medicines manufacturers and wholesale dealers in GB on selling and supplying products placed on the EU and UK markets before 1 January 2021 and the evidence you may need to provide.
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