# The Human Medicines Regulations 2012, Paragraph 8


If requested by the licensing authority, a summary of the product characteristics for the medicinal product in accordance with Part 2 of Schedule 8.

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Source: https://www.legislation.gov.uk/uksi/2012/1916/schedule/8A/paragraph/8 (the official version)
Page: https://openlegislation.uk/human-medicines-regulations-2012/schedule-8A/paragraph-8
Contains public sector information licensed under the Open Government Licence v3.0. Source: legislation.gov.uk, The National Archives.