# The Human Medicines Regulations 2012, Paragraph 2


The name of the medicinal product. This may be—
(a) an invented name that is not liable to confusion with the product’s common name; or
(b) a common or scientific name accompanied by a trademark or by the name of the person who is to be the parallel import licence holder.

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Source: https://www.legislation.gov.uk/uksi/2012/1916/schedule/8A/paragraph/2 (the official version)
Page: https://openlegislation.uk/human-medicines-regulations-2012/schedule-8A/paragraph-2
Contains public sector information licensed under the Open Government Licence v3.0. Source: legislation.gov.uk, The National Archives.