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Definitive fees charged for applications under Schedule 7 of the Veterinary Medicines Regulations 2013.
How to apply for or renew a Double Taxation Treaty Passport and how to tell HMRC about passported loans, for overseas lenders and UK borrowers.
Check how quickly you’ll receive a decision on your UK visa application if you are applying from outside the UK.
How the Northern Ireland Protocol affects supplementary protection certificates (SPCs), and what it means you need to do when applying for an SPC and afterwards.
Payments on account in civil cases, inquests, police station remote attendance, mental health tribunals, family hearings, and travel and mileage.
How to change the ownership from one marketing authorisation (MA) holder to another.
An overview of the process including submitting or fast tracking an application, naming your medicine and paying fees.
Make sure that domains that do not send email cannot be used for spoofing.
Renew, replace or apply for an adult or child British passport if you’re living abroad or working overseas - forms, prices, how long it takes
How to submit your periodic safety update report report (PSUR) or periodic benefit risk evaluation report (PBRER)
Find out about the changes if you are exporting personal protective equipment (PPE) during the coronavirus pandemic.
Licence and registration application information for companies that deal in precursor chemicals.
How to object to the registration of a lasting or enduring power of attorney - including forms and fees
Information to help you protect, manage and enforce your intellectual property (IP) rights in Colombia.
Guidance for the pharmaceutical industry on how to apply for an authorisation to place a veterinary medicine on the UK market or part of, or to expire one.
How someone in Poland can get documents prepared, witnessed or certified, take an oath of British citizenship and obtain informative notes.
Look up a trade mark to see if something identical or similar to your brand is already registered.
Check how much your visa application costs in the country you’re in
The UK Good Laboratory Practice Monitoring Authority (UK GLPMA) recognises that there are potential challenges COVID-19 will present to members of the GLP monitoring programme.
Guidance for organisations involved in any aspect of the pharmaceutical lifecycle or GLP studies regulated by MHRA, covering the approval of paper documents when working from home
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