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Register to vote Register by 18 June to vote in the General Election on 4 July.
Apply for an authorisation to manufacture extemporaneous preparations, autogenous vaccines, stem cell products or blood products for non-food animals.
This guidance provides information on comparator products used in studies supporting abridged marketing authorisation applications
Requirements for Marketing Authorisation applications for particular veterinary medicinal products.
What you need to know before you can place a medical device on the Great Britain market with a UKCA mark.
VICH consultation on the guideline relating to good manufacturing practice for active pharmaceutical ingredients used in veterinary medicinal products.
Advice on ingredients in nicotine-containing liquids in electronic cigarettes and refill containers.
How to apply for a traditional herbal registration (THR) to market a herbal medicine in the UK.
Marketing Authorisation Holders should review their manufacturing processes to identify and, if found, to mitigate the risk of nitrosamine impurities being present.
How to comply with the requirements on promoting medicines to the public and to prescribers and suppliers of medicines.
Requirements for Immunological Veterinary Medicinal Products.
Guidance for the veterinary pharmaceutical industry on the production of mock-ups for assessment.
An overview of the process including submitting or fast-tracking an application, naming your medicine and paying fees.
Requirements for Biological Veterinary Medicinal Products other than Immunological Veterinary Medicinal Products.
The MHRA is part of the Access Consortium along with the Therapeutic Goods Administration, Health Canada, Health Sciences Authority of Singapore and Swissmedic.
Requirements for an Animal Test Certificate (ATC) to carry out the field trial of a veterinary medicine in animals (clinical trial) in the UK.
How the MHRA makes decisions on when a product is a medical device (borderline products), and which risk class should apply to a medical device.
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