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Information about how approved bodies help regulate medical devices and how to apply for approval.
The locations for a Marketing Authorisation Holder (MAH) and a Qualified Person responsible for Pharmacovigilance (QPPV)
Apply for and maintain registrations for the brokering of human medicines.
Approved countries for batch testing and importation of medicines
Information for wholesale dealer licence holders about the medicines put on the UK market for UK patients that they cannot export or hoard.
This guide has been provided to reduce the burden when preparing responses to Post Inspection Letters.
The EU has published guidance on exemptions for medical devices manufactured and used within EU health institutions, which applies to Northern Ireland-based health institutions, replacing interim guidance from the MHRA.
Guidance on the steps manufacturers and suppliers can take to ease supply shortages.
How manufacturers can apply for approval to supply a non-compliant medical device on humanitarian grounds.
Guidance for industry on flexible approaches to regulation we are taking during the COVID-19 outbreak.
What you need to do to supply investigational medicinal products (IMPs) from Great Britain to Northern Ireland.
How and when to register updated packaging and information leaflets when new national marketing authorisations have been issued
Supplementary information for international regulators on packaging changes and the export of UK medicines.
How the 바카라 사이트˜Written Confirmation바카라 사이트™ process operates for active substances manufactured in Great Britain (England, Wales and Scotland).
Guidance to help medicine manufacturers meet safe limits on levels of nitrosamine impurities in medicines.
A series of webinars providing guidance on the Windsor Framework agreement and the supply of medicines in Northern Ireland.
On this page the Medicines and Healthcare Products Regulatory agency provides advice for producers of E-cigarette/vape products
Qualified Persons (QPs) should follow the below guidance on the flexible approaches we are taking for medicines imported from third countries.
Guidance on moving medicines by air
UK businesses can apply for a share of up to £8 million from the Industrial Strategy Challenge Fund for capital projects to improve medicines manufacturing.
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