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Departments, agencies and public bodies
News stories, speeches, letters and notices
Detailed guidance, regulations and rules
Reports, analysis and official statistics
Consultations and strategy
Data, Freedom of Information releases and corporate reports
Safety leaflet on topical corticosteroids and withdrawal reactions to help patients and their carers to use these medicines safely.
Check the tariff classification for flavour pods.
How to apply for a clinical trial including eligibility, phases, model IMPDs, costs and how to make changes to your application.
Information for patients, public and health care professionals.
A summary of recent letters and notifications sent to healthcare professionals about medicines and medical devices.
Business rates information letters are issued by the Department for Levelling Up, Housing and Communities at regular intervals throughout the year.
Information to assist with the laboratory diagnosis of Lyme disease and requirements for sample submission.
Information to support your recovery after COVID-19.
Information for clinicians and patients.
Guidance for industry on flexible approaches to regulation we are taking during the COVID-19 outbreak.
Get relief if you’re importing biological and chemical substances for research purposes from outside the EU and UK.
Check the tariff classification for components in sets for dental repair.
There are different regulations which apply to devices and equipment including hand gels and PPE (personal protective equipment)
Guidance for the veterinary pharmaceutical industry on the production and submission of the Summary of Product Characteristics (SPCs) and product literature mock-ups.
We handle shipping and maritime disputes. Cases that we hear include: collisions between ships disputes over the transport of cargo salvage of a ship, cargo or crew disputes over goods supplied to a ship disputes over mortgages and other security...
How the MHRA makes decisions on when a product is a medical device (borderline products), and which risk class should apply to a medical device.
How a marketing authorisation holder should report a defect with a veterinary medicine.
Substances that are classed as persistent organic pollutants (POPs) and when you're allowed to use them.
Applications received to amend the specification of a patent under sections 27 and 75 before the court and the Office.
You can claim relief to pay no Customs Duty and VAT if you're importing therapeutic substances of human origin, blood-grouping or tissue-typing reagents, or related packaging, solvents and accessories.
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