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How to account for VAT on goods and services provided by registered health professionals, including doctors, dentists, nurses and pharmacists.
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 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.
Guidance for industry on flexible approaches to regulation we are taking during the COVID-19 outbreak.
There are different regulations which apply to devices and equipment including hand gels and PPE (personal protective equipment)
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.
Legal requirements and good practice guidance for Veterinary Practice Premises Inspections.
The MSA is a unit of the Defence Logistics Organisation responsible for the provision of medical, dental and veterinary supplies to the Armed Forces.
What you need to know before you can place a medical device on the Great Britain market with a UKCA mark.
How to apply for a clinical trial including eligibility, phases, model IMPDs, costs and how to make changes to your application.
Information and guidance on a range of medical devices for users and patients.
Work out the VAT liability of goods and services supplied by health and care institutions and providers of non residential care to children.
This research included interviews in 2013–14 with 17 manufacturers and distributors
Guide for overseas investors on how to access NHS procurement channels.
The requirements for 3D printed products will depend on whether they are classed as medical devices, personal protective equipment (PPE) or both.
How to show MHRA you're meeting good clinical practice (GCP) standards and what to expect from an inspection.
Information on how to request assistance from NSDR.
Information for manufacturers of medical devices about reporting adverse incidents and field safety corrective actions to the MHRA.
Comply with good manufacturing practice (GMP) and good distribution practice (GDP), and prepare for an inspection.
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