# The Human Medicines Regulations 2012, Paragraph 18: Use of internationally agreed terminology, formats and standards


The licensing authority may publish a list of which of the internationally agreed—
(a) terminology; and
(b) formats and standards,
are to be used for the description, classification, retrieval, presentation, risk-benefit evaluation and assessment, electronic exchange and communication of pharmacovigilance and medicinal product information.

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Source: https://www.legislation.gov.uk/uksi/2012/1916/schedule/12A/paragraph/18 (the official version)
Page: https://openlegislation.uk/human-medicines-regulations-2012/schedule-12A/paragraph-18
Contains public sector information licensed under the Open Government Licence v3.0. Source: legislation.gov.uk, The National Archives.