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|Articles|November 8, 2011
MHRA Drives for Regulatory Excellence
Author(s)BioPharm International Editors
The Medicines and Healthcare products Regulatory Agency (MHRA) launched a public consultation on the consolidation of United Kingdom (UK) medicines legislation on Oct. 26, 2011.
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The Medicines and Healthcare products Regulatory Agency (MHRA)
In a press statement, MHRA Chief Executive, Sir Kent Woods, said, “Medicines legislation, which has been amended many times over several decades, can be greatly simplified by consolidation. The current need for this has received widespread support from both pharmacists and the pharmaceutical industry.
“It will amalgamate 40 years of outdated and fragmented legislation, reducing it by around two thirds, making it clearer and easier to understand as well as ensuring that medicines regulation is supported by a modern and straightforward legal framework.”
The consolidation is key to the MHRA’s Regulatory Excellence program, which examines regulations to ensure they are fit for purpose, and has the support of the Association of British Pharmaceutical Industry (ABPI). Stephen Whitehead, ABPI’s chief executive, said, “The ABPI welcomes this opportunity to contribute to providing clearer legislation and encourages our members to actively participate in the consultation.”
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