Paragraph 169
In regulation 213 (amendment of regulation 281 (duties of authorisation holders and registration holders)) for paragraphs (b) and (c) substitute—
“(b)omit “or” at the end of sub-paragraph (c); and
(c)in sub-paragraph (d), after “for a medicinal product” insert—
“; or
(e)an EU marketing authorisation for a medicinal product.”.”.