# The Human Medicines Regulations 2012, Paragraph 21: Format of electronic transmission of suspected adverse reactions


Holders must use the formats and terminology specified in the list published under paragraph 18 for the electronic transmission of suspected adverse reactions, if the licensing authority has published a list under that paragraph.

---
Source: https://www.legislation.gov.uk/uksi/2012/1916/schedule/12A/paragraph/21 (the official version)
Page: https://openlegislation.uk/human-medicines-regulations-2012/schedule-12A/paragraph-21
Contains public sector information licensed under the Open Government Licence v3.0. Source: legislation.gov.uk, The National Archives.