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Project Orbis is a programme to review and approve promising cancer drugs helping patients access treatments faster.
As with all products, the MHRA will keep its safety under close review.
This statistical bulletin presents a summary of mefloquine prescribing following the introduction of a new policy in September 2016.
The Medicines and Healthcare products Regulatory Agency (MHRA) has approved elafibranor (Iqirvo) to treat adult patients with a rare type of liver disease known as primary biliary cholangitis (PBC).
As with any medicine, the MHRA will keep the safety and effectiveness of seladelpar under close review.
How to apply for a clinical trial including eligibility, phases, model IMPDs, costs and how to make changes to your application.
Aspar Pharmaceuticals Limited have informed the MHRA of an error related to a batch of Boots Paracetamol 500 mg tablets (16s). The foil blister inside the carton incorrectly states ‘Aspirin 300 mg Dispersible Tablets’. The tablets are confirmed to be...
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