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An overview of the process including submitting or fast tracking an application, naming your medicine and paying fees.
Protocols and procedures for testing the distinctiveness, uniformity and stability (DUS) of certain agricultural and vegetable plants.
Look up a trade mark to see if something identical or similar to your brand is already registered.
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
Explainer for the pharmaceutical industry on the implementation of the Veterinary Medicines Regulation relating to Pharmacovigilance.
Guidance for industry on flexible approaches to regulation we are taking during the COVID-19 outbreak.
Information to help you protect, manage and enforce your intellectual property (IP) rights in China.
Monitor the progress of a patent application through search reports, open to the public inspection files, and caveats.
Find schemes that have told HMRC they meet the conditions to be a recognised overseas pension scheme (ROPS).
Sets out COVID-19 testing for hospice patients and staff.
Advice for medical professionals to follow when assessing drivers with neurological disorders.
Use the rolling review route when you want to submit your eCTD dossier in separate parts for pre-assessment instead of making a full consolidated document submission.
You can make observations on the patentability of a published patent application.
Check the patents journal to find UK-registered patents granted, published and filed
Use this form to transform your Madrid Protocol Designation to a UK Trade Mark application.
Guidance for exporting nuclear equipment, material and technology that appears on what is known as the 'Trigger List'.
Information to help you protect, manage and enforce your intellectual property (IP) rights in the European Union and the European Economic Area (EEA).
How to apply for repayment of import duty and VAT on protective equipment or medical supplies brought into the UK from non-EU countries from 30 January 2020 up to 31 December 2020.
Information about how to register your homeopathic medicinal product through the Simplified Homeopathic Registration Scheme or the UK Homeopathic National Rules Scheme
Guidance on the decentralised and mutual recognition reliance procedure (MRDCRP) for marketing authorisation applications including information on how to apply.
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