Since 1864, the British Pharmacopoeia has been providing authoritative official standards for pharmaceutical substances and medicinal products. The BP 2011 continues this tradition. It makes an important contribution, therefore, to the role of the Medicines and Healthcare products Regulatory Agency in protecting public health by setting publicly available standards for the quality of medicines. The new edition sees a significant rise in the numbers of monographs published for licensed formulated products. Control of the quality of unlicensed medicines is also improved by the provision of further standards, together with a new Supplementary Chapter containing well-established formulae, for extensively used unlicensed medicines for those healthcare professionals who formulate and prepare unlicensed medicines.
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