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Guidance on the submission and content of notifications for Northern Ireland
Guidance for industry on preparing responses to good laboratory practice (GLP) and good clinical practice (GCP) laboratory inspection reports.
To celebrate International Women’s Day 2023, some of our colleagues have shared their passion for STEM.
£500k is available to fund the development of novel PoC diagnostics devices.
Types of ingredients permitted in nicotine-containing liquids in electronic cigarettes and refill containers.
Notification Fees for Great Britain and Northern Ireland
Sets out the payment due from members of the voluntary scheme for branded medicines pricing and access in 2020.
To share a common understanding of the objectives and the operations of the Access Consortium - Generic Medicines Working Group (GMWG).
General advice on due diligence - electronic cigarettes devices and refill containers.
Access Consortium Statement on Good Manufacturing Practice (GMP) Inspections Reliance and Recognition
Industry must notify the MHRA if they will not be using these flexibilities
The Medicines and Healthcare products Regulatory Agency regulates medicines, medical devices and blood components for transfusion in the UK.
The UK Good Laboratory Practice Monitoring Authority (UK GLPMA) recognises that there are potential challenges COVID-19 will present to members of the GLP monitoring programme.
How to test and report levels of nicotine uptake when submitting a notification of intent to market e-cigarette and vape products.
A unique initiative which aims to accelerate the time to patient care for transformative medicines and medicine-device combinations.
UK government interpretation of the requirements for labelling e-liquids for Northern Ireland.
The types of emissions a manufacturer or importer of e-cigarettes should notify us about.
From discovery to real-world impact, VDEC equips scientists with the expertise and facilities to navigate each step in the development of vaccines and therapeutics.
Information for manufacturers and users of medical devices containing plastic with DEHP phthalates.
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