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This consultation invites views on the proposed steps we intend to take to make sure the UK meets its obligations to transpose the 'safety features' provisions of the Falsified Medicines Directive (FMD).
This consultation seeks views on proposed changes to the statutory scheme to control the costs of branded health medicines.
First published during the 2016 to 2019 May Conservative government
How the government will improve patient access to breakthrough technologies and treatments in response to recommendations by the AAR.
MHRA is asking for feedback on proposals to change the legal classification of Otrivine extra dual relief nasal spray solution from prescription only medicine (POM) to pharmacy only (P).
MHRA is asking for feedback on a proposal to simplify the information requirements for advertisements aimed at prescribers and suppliers of medicines.
This consultation welcomes views on proposals to revoke ‘The Clinical Thermometers (EEC Requirements) Regulations 1993’ by November 2014.
MHRA has published a business engagement assessment on Composite Coordination Collection (CCC).
The MHRA is seeking views on the proposal on the introduction of tell-and-do variations for a specific subset of parallel import licences.
The Department of Health and the MHRA are seeking views on this proposal by the European Commission.
First published during the 2010 to 2015 Conservative and Liberal Democrat coalition government
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