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Drug Regulators, MHRA, Publish Consultation, Intention to Amend the Medicines for Human Use Regulations 2008 (SI2008/1692)

Drug Regulators, MHRA, Publish Consultation, Intention to Amend the Medicines for Human Use Regulations 2008 (SI2008/1692)

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This consultation notifies interested parties that further amendments will be made to the Medicines For Human Use (Prescribing By EEA Practitioners) Regulations 2008
(2008 Regulations). This consultation seeks views on how current guidance can be expanded to provide additional support for community pharmacists following forthcoming legislative changes.

This consultation abides by the seven consultation criteria as set out in the revised Code of Practice on Consultation and which are summarised at Annex A. As the further
amendments to legislation are required for the purpose of complying with the views of the European Commission, a period of consultation of 4 weeks, although shorter than usually expected, is appropriate. Also, as those most affected by the further amendments to the 2008 Regulations will be members of the pharmacy profession, the consultation is being directed primarily to representatives of that profession, in addition to similar bodies representing medical, dental and other interests. However replies from other parties are welcome..

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