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There are different regulations which apply to devices and equipment including hand gels and PPE (personal protective equipment)
Information and guidance on a range of medical devices for users and patients.
How to register your medical devices with the Medicines and Healthcare products Regulatory Agency (MHRA) for the markets in Great Britain and Northern Ireland
Leicester business Unimed Procurement Services secured government-backed financing to help it deliver life-saving medical equipment around the world.
Advice on writing clear notices and maximising replies to your FSNs.
How to account for VAT on goods and services provided by registered health professionals, including doctors, dentists, nurses and pharmacists.
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.
The MSA is a unit of the Defence Logistics Organisation responsible for the provision of medical, dental and veterinary supplies to the Armed Forces.
Information for manufacturers of medical devices about reporting adverse incidents and field safety corrective actions to the MHRA.
From brussels sprouts to dodgy diet products, these tips from the MHRA will help you stay safe during the festive season and beyond
Order a certificate of free sale to export medical devices outside the UK.
How to comply with the requirements on promoting medicines to the public and to prescribers and suppliers of medicines.
Work out the VAT liability of goods and services supplied by health and care institutions and providers of non residential care to children.
Guidelines to help mitigate and manage medicine shortages.
Find out when it's possible to get zero-rated supplies on medical and research goods and services that have been funded by charities.
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.
Report a problem ('adverse incident') with a medical device or medicine to MHRA using the Yellow Card Scheme
What you need to know before you can place a medical device on the Great Britain market with a UKCA mark.
Information on the measures in the Health Service Medical Supplies (Costs) Bill.
Information for healthcare professionals on how pulse oximeters are regulated, home use and issues to look out for when using the devices
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