# The Human Medicines Regulations 2012, Regulation 53: Application for UKMA(NI) relating to similar biological medicinal products


(1) This regulation applies if an applicant for a UKMA(NI) for a biological medicinal product is not able to show that product meets a condition for its being a generic version of a similar medicinal product because of any of the reasons described in Article 10(4) of the 2001 Directive.
(2) The applicant must provide information in accordance with Article 10(4) and (6) of the 2001 Directive.
(3) Paragraph (2) of regulation 51 applies to the application as it applies in relation to an application made in accordance with paragraph (1) of that regulation.

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Source: https://www.legislation.gov.uk/uksi/2012/1916/regulation/53 (the official version)
Page: https://openlegislation.uk/human-medicines-regulations-2012/regulation-53
Contains public sector information licensed under the Open Government Licence v3.0. Source: legislation.gov.uk, The National Archives.