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An overview of the process including submitting or fast tracking an application, naming your medicine and paying fees.
How to apply for an exemption to use a restricted substance to manufacture electrical and electronic equipment.
Find out if you need an Academic Technology Approval Scheme (ATAS) certificate to study in the UK.
How to change the ownership from one marketing authorisation (MA) holder to another.
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
How to carry out a clinical trial to apply for a marketing authorisation, manage your authorisation and report safety issues.
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.
How contracting authorities can find approved specialist providers and award contracts for decontamination services in relation to a CBRN or major HazMat incident.
You must include the appropriate legal basis for your application when you apply to MHRA for a marketing authorisation.
How to use A/B testing to evaluate your digital health product.
Check the tariff classification for flavour pods.
Use a global project licence to simplify the export of military goods and technology classed as collaborative defence projects.
Further measures to be introduced to ensure patients who are prescribed montelukast for the treatment of asthma are informed of the risk of neuropsychiatric reactions
Goods that are controlled and how to get licences for them, the UK Strategic Export Control Lists, dealing with the Export Control Organisation (ECO).
You can make observations on the patentability of a published patent application.
Guidance for industry on flexible approaches we are taking on good distribution practices.
Details of certificates issued under the Special Import System for the top ten veterinary medicines that were imported 1 Oct - 31 Dec 2023.
Guidance for the pharmaceutical industry on Marketing Authorisations for veterinary medicines.
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