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An overview of the process including submitting or fast tracking an application, naming your medicine and paying fees.
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.
Protocols and procedures for testing the distinctiveness, uniformity and stability (DUS) of certain agricultural and vegetable plants.
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
Information on how to gain a UK CoC for Engineering/Electro-Technical Officers or Engineering Watch Rating Certificate
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.
Investors and businesses may be legally required to tell the government about certain sensitive acquisitions under the National Security and Investment Act.
Explainer for the pharmaceutical industry on the implementation of the Veterinary Medicines Regulation relating to Pharmacovigilance.
Information on how to gain a UK CoC for working Deck and Engineering Officers working on board merchant vessels and yachts.
Information to help you protect, manage and enforce your intellectual property (IP) rights in China.
Guidance for industry on flexible approaches to regulation we are taking during the COVID-19 outbreak.
Monitor the progress of a patent application through search reports, open to the public inspection files, and caveats.
Licence and registration application information for companies that deal in precursor chemicals.
Use this form to transform your Madrid Protocol Designation to a UK Trade Mark application.
How to apply for an exemption to use a restricted substance to manufacture electrical and electronic equipment.
Class and permitted use of passenger ships, cargo ships, tankers, tugs, tenders, fishing boats, yachts, commercial vessels, and the required certificates.
Guidance for the pharmaceutical industry on how to apply to vary a veterinary Marketing Authorisation (MA) or Homeopathic Remedy.
Information to help you protect, manage and enforce your intellectual property (IP) rights in the European Union and the European Economic Area (EEA).
Apply for a promising innovative medicine (PIM) designation or scientific opinion for your medicine from MHRA.
Project Orbis is a programme to review and approve promising cancer drugs helping patients access treatments faster.
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