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Register to vote Register by 18 June to vote in the General Election on 4 July.
The mycology reference laboratory (MRL) provides a comprehensive laboratory service for the diagnosis and management of fungal infections.
Guidance on Conditional Marketing Authorisations, exceptional circumstances Marketing Authorisations and national scientific advice
Check the tariff classification for surface-active preparation for washing the skin and the hair (gel 2-in-1).
Licences and authorisations to import genetic material, research and diagnostic samples, trade samples and display items, and some live animals and animal products.
Foreign, Commonwealth & Development Office (FCDO) guidance on preventing and responding to sexual exploitation, abuse and harassment in the international aid sector.
Check the tariff classification for preparations put up for retail sale.
Emerging techniques on how to prevent or minimise the environmental impacts of industrial hydrogen production from methane or refinery fuel gas with carbon capture for storage.
Guidance on who to test for Zika virus infection and which samples to collect.
Find out how you can use, process or store similar free circulation goods in place of goods that you have declared for a customs special procedure.
How we engage and involve patients and the public in our regulatory decision-making.
Actions that trial sponsors should consider to build resilience into clinical trial design
Apply for a promising innovative medicine (PIM) designation or scientific opinion for your medicine from MHRA.
Guide to licensing procedure and other restrictions for export of controlled dual-use items, software and technology, goods for torture and radioactive sources.
A wholesale dealer in Great Britain may import Qualified Person certified medicines from the European Economic Area if certain checks are made by the ‘Responsible Person (import)’
Reported problems with the supply of an animal medicine and the date when the issue is expected to be resolved.
Guidance for the pharmaceutical industry on Marketing Authorisations for veterinary medicines 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.
Find out how you could do the SFI actions for soils.
Placing a veterinary medicine on the market, including non-medicinal products, medicinal words and phrases, how to obtain advice, report non-compliance.
The way you apply to licence biological products has changed
Don’t include personal or financial information like your National Insurance number or credit card details.
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