# The Human Tissue (Quality and Safety for Human Application) Regulations 2007, Paragraph 4A


Directions must require that importing licence holders are required to—
(a) notify the Authority of any serious adverse events or serious adverse reactions notified to the importing licence holder by that person’s third country supplier (including events or reactions which that supplier suspects are serious adverse events or reactions); and
(b) provide any information specified in the direction which the Authority requires for the purposes of securing compliance with the requirements of Article 6(2) of the fourth Directive (updated information).

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Source: https://www.legislation.gov.uk/uksi/2007/1523/schedule/2/paragraph/4A (the official version)
Page: https://openlegislation.uk/human-tissue-quality-and-safety-for-human-application-regulations-2007/schedule-2/paragraph-4A
Contains public sector information licensed under the Open Government Licence v3.0. Source: legislation.gov.uk, The National Archives.