Paragraph 169 I1

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.”.”.