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Deficiencies in Omega’s pharmacovigilance system are not thought to affect the safety of the products that they market.
Which submission type to select when submitting a notification of intent to market e-cigarette and vape products in Northern Ireland.
Acceptable naming, presentation and packaging of nicotine-containing electronic cigarettes and refill containers.
Submitting annual reports on sales of electronic cigarettes and refill containers.
Due diligence for suppliers of e-cigarettes and e-liquids.
Information about the types of content published by the MHRA.
Guidance on the submission and content of notifications for Northern Ireland
Report showing opportunities and challenges for community pharmacy teams to further support the public’s health.
£500k is available to fund the development of novel PoC diagnostics devices.
The findings and recommendations of the Expert Advisory Group on paclitaxel drug-coated balloon catheters and drug-eluting stents which are used to treat patients with peripheral arterial disease.
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.
Briefing for local authorities on the increasing role of community pharmacy in public health, working with councils and other community partners.
Access Consortium Statement on Good Manufacturing Practice (GMP) Inspections Reliance and Recognition
The Medicines and Healthcare products Regulatory Agency regulates medicines, medical devices and blood components for transfusion in the UK.
How to test and report levels of nicotine uptake when submitting a notification of intent to market e-cigarette and vape products.
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.
Information for pharmaceutical wholesalers explaining the main changes the Windsor Framework introduces to the packaging for all medicines licensed in the UK, effective from 1 January 2025.
Information and advice on submitting a dermatological product to the Advisory Committee for Borderline Substances (ACBS).
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