# The Medicines (Marketing Authorisations Etc.) Amendment Regulations 2005, Paragraph 18


In the General Product Safety Regulations 2005 in regulation 33 (duty to notify), in paragraph (10)(b), after “human use”, insert “as amended by Directive 2002/98/EC of the European Parliament and of the Council setting standards of quality and safety for the collection, testing, processing, storage and distribution of human blood and blood components, Commission Directive 2003/63/EC amending Directive 2001/83/EC on the Community code relating to medicinal products for human use, Directive 2004/24/EC of the European Parliament and of the Council amending, as regards traditional herbal medicinal products, Directive 2001/83/EC on the Community code relating to medicinal products for human use and Directive 2004/27/EC of the European Parliament and of the Council amending Directive 2001/83/EC on the Community code relating to medicinal products for human use”.

---
Source: https://www.legislation.gov.uk/uksi/2005/2759/schedule/paragraph/18 (the official version)
Page: https://openlegislation.uk/medicines-marketing-authorisations-etc-amendment-regulations-2005/schedule/paragraph-18
Contains public sector information licensed under the Open Government Licence v3.0. Source: legislation.gov.uk, The National Archives.