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Apply for changes to your marketing authorisation, including minor variations type IA and IB, major variations type II and extensions.
Pharmacovigilance system requirements
Make sure that domains that do not send email cannot be used for spoofing.
An overview of the process including submitting or fast tracking an application, naming your medicine and paying fees.
This information is provided to help British nationals make decisions about getting medical advice and reporting a rape or sexual assault in Russia.
How contracting authorities can find approved specialist providers and award contracts for decontamination services in relation to a CBRN or major HazMat incident.
Look up a trade mark to see if something identical or similar to your brand is already registered.
You must tell DVLA if you have a brain abscess, cyst or encephalitis - download the correct form to let them know
Form (E13): polyomavirus investigation.
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
How to use A/B testing to evaluate your digital health product.
Monitor the progress of a patent application through search reports, open to the public inspection files, and caveats.
Get help to classify pharmaceutical products used to treat or prevent diseases or ailments (in humans or animals), including comparators used in clinical trials and placebos.
Explainer for the pharmaceutical industry on the implementation of the Veterinary Medicines Regulation relating to Pharmacovigilance.
Use a global project licence to simplify the export of military goods and technology classed as collaborative defence projects.
How to carry out a clinical trial to apply for a marketing authorisation, manage your authorisation and report safety issues.
You must include the appropriate legal basis for your application when you apply to MHRA for a marketing authorisation.
Information and guidance on a range of medical devices for users and patients.
Information to help you protect, manage and enforce your intellectual property (IP) rights in the European Union and the European Economic Area (EEA).
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