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Register to vote Register by 18 June to vote in the General Election on 4 July.
Guidance for the pharmaceutical industry on Marketing Authorisations for veterinary medicines in the UK.
Use this form when paying for consular services with credit card in Brazil.
Guidance on Conditional Marketing Authorisations, exceptional circumstances Marketing Authorisations and national scientific advice
British travellers to the US must register with the Electronic System for Travel Authorisation (ESTA) before their journey
Apply for changes to your marketing authorisation, including minor variations type IA and IB, major variations type II and extensions.
Authorisation decisions on the time-limited use of hazardous substances of very high concern under UK REACH.
To help you protect, manage and enforce your intellectual property (IP) rights in Laos.
How to renew marketing authorisations for products granted through different routes and at different times.
How to apply for a clinical trial including eligibility, phases, model IMPDs, costs and how to make changes to your application.
This guidance is for HM Passport Office staff.
This guidance is for His Majesty’s Passport Office staff.
How to apply for marketing authorisation via this new procedure.
The process for the simultaneous review of veterinary drug submissions by Health Canada’s Veterinary Drugs Directorate and the UK's Veterinary Medicines Directorate.
Apply for an authorisation to manufacture extemporaneous preparations, autogenous vaccines, stem cell products or blood products for non-food animals.
There are different ways to register depending on which tax service you want to use on behalf of your client.
How to get a marketing authorisation for an Advanced Therapy Medicinal Product (ATMP) so it can be sold and/or supplied in Great Britain.
Find out how to declare that your goods have been put to their authorised use, destroyed or re-exported.
Check if you can apply for Authorised Use relief to reduce your payments when you import goods for a specific use. This can include repairs, maintenance or processing.
Information for manufacturers of medical devices about reporting adverse incidents and field safety corrective actions to the MHRA.
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