Regulation 10 Amendment of regulation 60A (condition as to the submitting of samples and other information to the appropriate authority)

Regulation 60A^f1 is amended as follows.

In paragraph (1), in the definition of “the batch testing exemption”, in paragraph (b)(ii), after “United Kingdom” insert “or, in the case of a product for sale or supply in Northern Ireland, the European Union”.

In paragraph (2), in each place where it occurs, for “immunological product” substitute “immunological medicinal product”.