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Legal terms for veterinary medicines, marketing of non-medicinal products including medicinal words and phrases, how to complain.
Information and resources.
How the MHRA makes decisions on what is a medicinal product (borderline products).
Guidance for the pharmaceutical industry on how to apply to vary a veterinary Marketing Authorisation (MA) or Homeopathic Remedy.
Guidance on how to license electronic cigarettes and other inhaled nicotine-containing products (NCPs) as medicines in the UK.
Use a separate statement of objection form for each Japanese GI product name you object to.
Search for information about medicines including patient information leaflets (PILs), details on how the medicine can be used (SmPCs) and scientific reports (PARs).
Submission dates and how the submissions using the EC decision reliance procedure work.
There are changes to the legislation of Reference Medicinal Products (RMPs) used to support abridged marketing authorisation applications
Get help classifying computers, inkjet and toner cartridges and their components.
Guidance for the veterinary pharmaceutical industry on the production of mock-ups for assessment.
How to ensure the products you make or import comply with the law and are safe for consumers to use.
Guidance on Conditional Marketing Authorisations, exceptional circumstances Marketing Authorisations and national scientific advice
Information to support commercial fishers on under 12 metre English vessels.
How to prepare for implementation and compliance of the Safety Features Regulation.
How to make sure that your products are properly checked for conformity and your technical documents are managed correctly.
Information on OPSS product safety alerts, reports and recalls for unsafe products and resources for consumers, businesses and regulators.
Directory of current ICH Guidelines which have been implemented by the Medicines and Healthcare products Regulatory Agency.
How to get fast-track approval of medical devices during COVID-19.
The MHRA will review applications for orphan designation at the time of a marketing authorisation (MA) or variation application.
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