The Human Fertilisation and Embryology (Quality and Safety) Regulations 2007

General conditions

13.—(1) Section 12 (general conditions) is amended as follows.

(2) Make the existing provision subsection (1).

(3) In that subsection—

(a) in paragraph (a), for “that the activities authorised by the licence” substitute “except to the extent that the activities authorised by the licence fall within paragraph (aa), that those activities”,

(b) after paragraph (a) insert—

“(aa) that any activities to which section 3(1A)(b) or (1B) or 4(1A) applies shall be carried on only on the premises to which the licence relates or on relevant third party premises,”, and

(c) at the beginning of paragraph (c) insert “except in relation to the use of gametes in the course of providing basic partner treatment services or non-medical fertility services,”.

(4) After that subsection, insert—

“(2) Subsection (3) applies to—

(a) every licence under paragraph 1 or 1A of Schedule 2, and

(b) every licence under paragraph 2 of that Schedule, so far as authorising the storage of gametes or embryos intended for human application.

(3) It shall be a condition of every licence to which this subsection applies that—

(a) such information as is necessary to facilitate the traceability of gametes and embryos, and

(b) any information relating to the quality or safety of gametes or embryos,

shall be recorded and provided to the Authority upon request.”.