The European Commission has issued a consultation on guidelines on medicines distribution. These aim to take account of the amendments in Directive 2011/62/EU to substantive Directive 2001/83/EC, including arrangements to prevent the entry into the legal supply chain of “fasified medicinal products”. Consultation closes on 31st December 2011 with a view to implementation 6 months after publication of final guidelines

The GPhC has started informal discussion on its future policy and standards for pharmacy premises. Formal consultation is expected later in 2011 but responses should be made now to their information document. Comments are invited on the registration criteria that may be appropriate for different kinds of pharmacy, on standards for superintendents and owners, inspections and areas where detailed standards (formerly issued by RPSGB) are not planned.

A further “informal” consultation has been published arising from the review of medicines legislation.This seeks views on how to bring eligible homeopathic PLRs within a relevant regulatory scheme, to address the future of the Product Licence of Right (PLR) regime and clarify the position as regards efficacy of homeopathic products. Consultation closes on 18th February 2011.

A consultation, launched informally by the MHRA on 21st January seeks comment on guidance about the licensing and advertising of homeopathic products. Consultation closes 18th February 2011.

Consultation on proposal to remove the restriction on pharmacists registered in GB by virtue of an EEA or Swiss qualification, being the responsible pharmacist for a pharmacy which has been registered for less than three years. An order under section 73 of the Medicines Act is proposed. Further legislation will be needed to remove the restriction on “visiting pharmacists” (on a temporary or occasional basis) from the EU. Closes on 7th April 2011