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This is advice for UK sponsors whose students are affected by coronavirus (COVID-19).
Guidance for the pharmaceutical industry on how to apply to vary a veterinary Marketing Authorisation (MA) or Homeopathic Remedy.
Apply for a promising innovative medicine (PIM) designation or scientific opinion for your medicine from MHRA.
Check the patents journal to find UK-registered patents granted, published and filed
These temporary good manufacturing practice (GMP) flexibilities will be allowed to address the current exceptional circumstances
How the MHRA assesses Marketing Authorisation Applications (MAA) for medicines referred under Article 29.
Find out about tax charges on scholarships.
Explainer on product information templates to be used by applicants and Marketing Authorisation Holders (MAHs) of veterinary medicines.
Find details of recent trade mark applications or amendments by searching the journal
You can make observations on the patentability of a published patent application.
Form to apply to export seed which has met field seed standards but is not finally certified.
This is a work sharing model for the co-ordinated assessment of a generic application that has been filed with multiple Access Consortium agencies.
Information on COVID-19, including guidance on the assessment and management of suspected UK cases.
Guidance for the veterinary pharmaceutical industry on the production and submission of the Summary of Product Characteristics (SPCs) and product literature mock-ups.
Apply for a nutritional product to be considered by the Advisory Committee on Borderline Substances (ACBS).
Details of the exceptions to copyright that allow limited use of copyright works without the permission of the copyright owner.
Apply for a Student visa to study in the UK if you're 16 or over - eligibility, extend or switch your visa, how much it costs and how long it takes
A register of agreements relating to exclusion orders made by powers under paragraph 7 of Schedule 3 to The Competition Act 1998.
This guidance provides information on comparator products used in studies supporting abridged marketing authorisation applications
The following guidance has been jointly developed by the Heath Research Authority (HRA) and MHRA, in consultation with the Information Commissioners Office (ICO), on behalf of the UK.
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