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Directory of current ICH Guidelines which have been implemented by the Medicines and Healthcare products Regulatory Agency.
An overview of the future requirements for rapid COVID-19 diagnostic assays for antigen lateral flow devices.
Look up a trade mark to see if something identical or similar to your brand is already registered.
The MHRA has authorised cabotegravir as 30 mg tablets and as a 600 mg long-acting injection administered every two months
The guide, toolkit and further information for GB authorities with responsibility for consumer product safety.
Use a separate statement of objection form for each Japanese GI product name you object to.
Check the tariff classification for surface-active preparation for washing the skin and the hair (gel 2-in-1).
Decision on application for authorisation under UK REACH.
View designs registered in the designs journal from the last 25 years
How to apply for an exemption to use a restricted substance to manufacture electrical and electronic equipment.
Batch recall alert for human eye gels that may be prescribed by vets and used under the cascade.
Apply for a visa to visit the UK if you want to marry or register a civil partnership within 6 months - eligibility, documents, how to apply, how much it costs
Find out if you need an Academic Technology Approval Scheme (ATAS) certificate to study in the UK.
Information on COVID-19, including guidance on the assessment and management of suspected UK cases.
The Intellectual Property Office offers different methods of accelerating the processing of your patent application.
We are here to make digital government simpler, clearer and faster for everyone. GDS is part of the Cabinet Office .
Information on cleaning an oil spill including your options, how to get a product approved and how long it will take.
There are different regulations which apply to devices and equipment including hand gels and PPE (personal protective equipment)
Information about opinions requests we have received this year
These reports explain our assessment of the scientific evidence used to lead to regulatory decisions on the safety of medicines or medicines classes.
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