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Guidance for industry on flexible approaches to regulation we are taking during the COVID-19 outbreak.
You can make observations on the patentability of a published patent application.
We help people, businesses and the UK economy by promoting competitive markets and tackling unfair behaviour. CMA is a non-ministerial department.
Using recommended patterns for workplace wifi networks and sharing infrastructure.
Information to help you protect, manage and enforce your intellectual property (IP) rights in the European Union and the European Economic Area (EEA).
Use this form to transform your Madrid Protocol Designation to a UK Trade Mark application.
Find data and analysis from Census 2021 and earlier censuses.
Information for developing and testing of software for HMRC forms, returns and messages.
Guidance for the pharmaceutical industry on how to apply to vary a veterinary Marketing Authorisation (MA) or Homeopathic Remedy.
Calculate value build-up costs for use with the Single Administrative Document (SAD) using form C89.
How to classify and describe your business waste so you can know how to manage and dispose of it - what you need to do, List of Waste (LoW) codes, technical guidance.
Guidance for the pharmaceutical industry on Marketing Authorisations for veterinary medicines.
Configure email services securely using encryption and anti-spoofing.
Form A64A: Application to receive information from court records about a parental order.
Information on using the app to apply for an electronic travel authorisation (ETA) to come to the UK.
Guidance on the national tuberculosis (TB) strain typing service, including its work, achievements, objectives, and future direction.
Find details of recent trade mark applications or amendments by searching the journal
Guidance on the collection and reporting of data for CTAD, the surveillance system for all chlamydia tests done in England.
Applications received to amend the specification of a patent under sections 27 and 75 before the court and the Office.
How the MHRA assesses Marketing Authorisation Applications (MAA) for medicines referred under Article 29.
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