# The Human Medicines Regulations 2012, Regulation 256L: Variation of a person’s entry on the list on the application of that person


(1) This regulation applies if a person entered on the list applies to the licensing authority for a variation of the person’s entry on the list.
(2) The application must—
(a) be in writing;
(b) specify the variation requested;
(c) be signed by or on behalf of the applicant; and
(d) be accompanied by such information as may be required to enable the licensing authority to consider the application.
(3) The licensing authority must vary a person’s entry on the list or refuse to vary it within 30 days beginning with the day after the date when the licensing authority receives the application.
(4) The licensing authority may give a notice to the applicant requiring the applicant to supply further information in connection with the application within the period specified in the notice.
(5) If a notice under paragraph (4) requires the applicant to provide the licensing authority with information, the information period is not to be counted for the purposes of paragraph (3).
(6) In paragraph (5), the “information period” means the period—
(a) beginning with the day on which notice under paragraph (4) is given; and
(b) ending with the day on which the licensing authority receives the information or the applicant shows to the licensing authority's satisfaction that the applicant is unable to provide it.
(7) Nothing in this regulation affects the powers conferred by regulations 256I and 256K.

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Source: https://www.legislation.gov.uk/uksi/2012/1916/regulation/256L (the official version)
Page: https://openlegislation.uk/human-medicines-regulations-2012/regulation-256L
Contains public sector information licensed under the Open Government Licence v3.0. Source: legislation.gov.uk, The National Archives.