Regulation 3 Amendment of Schedule 2 to the principal Regulations

after paragraph (a) of sub-paragraph (3) there shall be inserted the following paragraph:

“(aa)

where there is in relation to the product which has been manufactured or assembled, a certificate of registration, to ensure that each batch of the product has been manufactured or assembled and checked in compliance with that certificate and the provisions of the Medicines (Homoeopathic Medicinal Products for Human Use) Regulations 1994^f1;”;

in paragraph (b) of sub-paragraph (3), after “(a)” there shall be inserted “or (as the case may be) (aa)”;

in sub-paragraph (5) the words “or to medicinal products that are homoeopathic products” shall be omitted.