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 …

UK patients could next year be given access to drugs that are still in the later stages of clinical development, …
No one looks forward to receiving a letter from the MHRA (Medicines and Healthcare products Regulatory Agency) inspectorate announcing their …
New guidelines from the Medicines and Healthcare Products Regulatory Agency (MHRA) have placed disease awareness campaigns under the spotlight.They spell …
NIHR chief scientific adviser visits Huddersfield health innovation campus
One in three UK women with migraine say symptoms taken less seriously
Report highlights scope to expand day surgery
Sygnature formalises drug discovery collaboration with X-Chem
Codis appoints Steven Facer as chief commercial officer

