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You may need to tell DVLA if you have peripheral arterial disease - download the correct form if you need to let them know
You must tell DVLA if you have peripheral neuropathy - download the correct form to let them know
A wholesale dealer in Great Britain may import Qualified Person certified medicines from the European Economic Area if certain checks are made by the ‘Responsible Person (import)’
Information and guidance on a range of medical devices for users and patients.
The Resilience Capabilities Programme aims to increase the capability to respond to and recover from civil emergencies and provides advice on preparing for a crisis.
Information for manufacturers of medical devices about reporting adverse incidents and field safety corrective actions to the MHRA.
Information about the EU Regulations and their implementation in Northern Ireland
Product security factsheet accompanying the Product Security and Telecommunications Infrastructure Bill, outlining the problems the Bill will address and how.
How to register your medical devices with the Medicines and Healthcare products Regulatory Agency (MHRA) for the markets in Great Britain and Northern Ireland
Check if you need to tell DVLA about a health or medical condition, how to report medical conditions to DVLA
Guidance for manufacturers, importers and distributors.
Guide to licensing procedure and other restrictions for export of controlled dual-use items, software and technology, goods for torture and radioactive sources.
An overview of the work the IPO is undertaking in relation to Standard Essential Patents.
How to get a parallel import licence for your medicine in the UK, including pharmacovigilance requirements and submitting your application.
Appendix to the assessing fitness to drive guide for medical professionals.
Advice for medical professionals to use when assessing drivers with cardiovascular disorders.
Licence and registration application information for companies that deal in precursor chemicals.
Find out about the rules for placing transportable pressure equipment on the market in Great Britain from 1 January 2023.
Pharmacovigilance system requirements
Directory of current ICH Guidelines which have been implemented by the Medicines and Healthcare products Regulatory Agency.
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