The UK has unilaterally adopted a policy of allowing imports of active pharmaceutical ingredients (API) on the strength of pharmaceutical …
A British scientist has become the first person to be jailed under the Good Laboratory Practice (GLP) Regulations 1999 for …

An ex-employee of research organisation Aptuit has been found guilty of changing pre-clinical trial data as part of a bid to …
Switzerland has become the first country to be classed as having equivalent standards for the manufacture of active pharmaceutical ingredients …

The European Medicines Agency is investigating Roche after ‘deficiencies’ in the manufacturer’s pharmacovigilance processes came to light. It has emerged …
The UK pharma industry’s Code of Practice is set to be updated to bring it into line with changes in …

The UK government’s drug safety regulator is calling on the pharma industry to help it eliminate unneccessary bureaucracy.The Medicines and …

The UK medicine regulatory authority has suspended the licence for a levothyroxine product sold by Teva on the grounds that …

The European Commission is seeking regulatory reform for class III medical devices after problems with French-made breast implants. The French …
Last week’s recall of Reckitt Benckiser’s painkiller product Nurofen Plus has been expanded after two additional cases emerged where powerful …
Consumers in the UK are being warned to double-check packs of Reckitt Benckiser’s painkiller product Nurofen Plus following reports that …
Pharmaceutical companies in the UK will have to declare the amount of money paid to its healthcare professionals who act …
The bonfire of the quangos has begun in earnest in the health sector, with 18 so-called “arm’s length bodies” cut …

From September all serious adverse events that occur during clinical trials in the UK will have to be reported electronically …

The MHRA is considering putting its database of patient information leaflets (PILs) and Summaries of Product Characteristics (SPCs) online and …