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Guidance on how to license electronic cigarettes and other inhaled nicotine-containing products (NCPs) as medicines in the UK.
What you need to know before you can place a medical device on the Great Britain market with a UKCA mark.
Apply for a Temporary Work - Creative Worker visa to work in the UK in the creative industry - eligibility, extend, bring your family.
Information to help you protect, manage and enforce your intellectual property (IP) rights in China.
Make sure that domains that do not send email cannot be used for spoofing.
The CMA investigated alleged excessive and unfair pricing, anti-competitive agreements and abusive conduct with respect to hydrocortisone tablets under Chapters I and II CA98 and Articles 101 and 102 TFEU.
Renew and pay for a GB or European patent online - when renewal is due, fees, renew by post or phone instead
Advice for medical professionals to follow when assessing drivers with neurological disorders.
Getting a faster decision on a visa or settlement application; priority service, super priority service; waiting times; how to check if you're eligible
Countries have their own rules about what goods you can bring in using an ATA Carnet. Check with the issuer in the country you’re exporting to.
Pharmacovigilance system requirements
Guidance on Conditional Marketing Authorisations, exceptional circumstances Marketing Authorisations and national scientific advice
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
We help people, businesses and the UK economy by promoting competitive markets and tackling unfair behaviour. CMA is a non-ministerial department.
How to make sure that your products are properly checked for conformity and your technical documents are managed correctly.
How to apply for authorisation to become a regulated claims company, understanding the fee structure, and how and when to pay fees.
Definitive fees charged for applications under Schedule 7 of the Veterinary Medicines Regulations 2013.
Information to help you protect, manage and enforce your intellectual property (IP) rights in Colombia.
The New Active Substance Work Sharing Initiative (NASWSI) has successfully approved several medicines through this international collaboration and continues to foster cooperation and strong relationships between its Access partners. The Biosimilar Work Sharing Initiative (BSWSI) builds on this success.
Information about the EU Regulations and their implementation in Northern Ireland
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