F2except to the extent that the activities authorised by the licence fall within paragraph (aa), that those activities shall be carried on only on the premises to which the licence relates and under the supervision of the person responsible,

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,

that any member or employee of the Authority, on production, if so required, of a document identifying the person as such, shall at all reasonable times be permitted to enter those premises and inspect them (which includes inspecting any equipment or records and observing any activity),

F4except in relation to the use of gametes in the course of providing basic partner treatment services F10... , that the provisions of Schedule 3 to this Act shall be complied with,

that proper records shall be maintained in such form as the Authority may specify in directions,

that no money or other benefit shall be given or received in respect of any supply of gametesF11, embryos or human admixed embryos unless authorised by directions,

that, where gametesF12, embryos or human admixed embryos are supplied to a person to whom another licence applies, that person shall also be provided with such information as the Authority may specify in directions, and

that the Authority shall be provided, in such form and at such intervals as it may specify in directions, with such copies of or extracts from the records, or such other information, as the directions may specify.

every licence under paragraph 1 or 1A of Schedule 2, F13...

every licence under paragraph 2 of that Schedule, so far as authorising the storage of gametes or embryos intended for human applicationF14, and

every licence under paragraph 3 of that Schedule, so far as authorising activities in connection with the derivation from embryos of stem cells that are intended for human application.

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

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

the persons for whom services are provided in pursuance of the licence,

the services provided for them,

the persons whose gametes are kept or used for the purposes of services provided in pursuance of the licence or whose gametes have been used in bringing about the creation of embryos so kept or used,

any child appearing to the person responsible to have been born as a result of treatment in pursuance of the licence,

any mixing of egg and sperm and any taking of an embryo from a woman or other acquisition of an embryo, and

such other matters as the Authority may specify in directions.

any man as respects whom the agreed fatherhood conditions in section 37 of the Human Fertilisation and Embryology Act 2008 (“the 2008 Act”) are for the time being satisfied in relation to treatment provided to the woman mentioned in subsection (6A), and

any woman as respects whom the agreed female parenthood conditions in section 44 of the 2008 Act are for the time being satisfied in relation to treatment provided to the woman mentioned in subsection (6A).

the importance of informing any resulting child at an early age that the child results from the gametes of a person who is not a parent of the child, and

suitable methods of informing such a child of that fact.

must notify W in writing of the receipt of the notice from X, and

no person to whom the licence applies may place an embryo or sperm and eggs in W, or artificially inseminate W, until W has been so notified.

notice under section 37(1)(c) or 44(1)(c) of the 2008 Act of the withdrawal of W's consent, or

a notice under section 37(1)(b) or 44(1)(b) of the 2008 Act in respect of a person other than X,

for determining the persons providing gametes or from whom embryos are taken for use in pursuance of the licence, and

for the purpose of securing that consideration is given to the use of practices not requiring the authority of a licence as well as those requiring such authority.

the persons who are to provide gametes for use in pursuance of the licence in a case where consent is required under paragraph 5 of Schedule 3 for the use in question;

the woman from whom an embryo is to be taken for use in pursuance of the licence, in a case where her consent is required under paragraph 7 of Schedule 3 for the use of the embryo;

which of two or more embryos to place in a woman.

a serious physical or mental disability,

a serious illness, or

any other serious medical condition,

a gender-related serious physical or mental disability,

a gender-related serious illness, or

any other gender-related serious medical condition,

it affects only one sex, or

it affects one sex significantly more than the other.

that an embryo the creation of which has been brought about in vitro otherwise than in pursuance of that licence shall be placed in storage only if acquired from a person to whom a licence or third party agreement applies,

that a human admixed embryo the creation of which has been brought about in vitro otherwise than in pursuance of that licence shall be placed in storage only if acquired from a person to whom a licence under paragraph 2 or 3 of Schedule 2 applies,

that gametes or embryos which are or have been stored shall not be supplied to a person otherwise than in the course of providing treatment services unless that person is a person to whom a licence applies,

that human admixed embryos shall not be supplied to a person unless that person is a person to whom a licence applies,

that the requirements of subsection (3) (maximum storage periods) are met,

that any gametes, embryos or human admixed embryos that have been kept in storage pursuant to the licence must, once they may no longer lawfully be so kept, be removed from storage and disposed of, and

that such information as the Authority may specify in directions as to the persons whose consent is required under Schedule 3 to this Act, the terms of their consent and the circumstances of the storage and as to such other matters as the Authority may specify in directions shall be included in the records maintained in pursuance of the licence.

gametes must not be kept in storage for longer than such period not exceeding 55 years beginning with the day on which they are first placed in storage as the licence may specify;

an embryo must not be kept in storage for treatment purposes for longer than such period not exceeding 55 years beginning with the day on which it is first so kept as the licence may specify;

an embryo that is kept in storage for the research or training purpose but not for treatment purposes must not be so kept for longer than such period not exceeding 10 years beginning with the day on which consent was given under Schedule 3 to the storage of the embryo for that purpose as the licence may specify;

a human admixed embryo must not be kept in storage for longer than such period not exceeding 10 years beginning with the day on which it is first placed in storage as the licence may specify.

“treatment purposes” are purposes referred to in paragraph 2(1)(a) or (b) of Schedule 3;

the “training purpose” is the purpose referred to in paragraph 2(1)(ba) of that Schedule;

the “research purpose” is the purpose referred to in paragraph 2(1)(c) of that Schedule.

every licence under paragraph 1 or 1A of Schedule 2, F23...

every licence under paragraph 2 of that Schedule, so far as authorising storage of gametes or embryos intended for human applicationF24, and

every licence under paragraph 3 of that Schedule, so far as authorising activities in connection with the derivation from embryos of stem cells that are intended for human application.

any premises to which a licence relates and any relevant third party premises to be inspected on its behalf, and

a report on the inspection to be made to it.

qualifying gametes or embryos are imported into F30Northern Ireland from a third country by an importing licensee,

the gametes or embryos are distributed in an EEA state F31..., and

make arrangements with the competent authority which made the request under subsection (1) for it to participate in the inspection, or

notify the competent authority which made the request under subsection (1) that the Authority has decided that it is not appropriate for it to participate in the inspection and give reasons for that decision.

an inspection of any third country premises,

an inspection of any relevant documents held by a third country supplier.

inspecting any equipment found on the premises,

inspecting and taking copies of any relevant documents or records found on the premises, and

observing the carrying on of any activity relevant to ascertaining whether qualifying gametes or embryos imported from a third country meet standards of quality and safety equivalent to those laid down in this Act.

a copy of a report or information on any inspection of third country premises or relevant documents carried out in pursuance of section 15B(2) or (5),

information on any exercise of the Authority’s powers under section 18(2), 18A(3) or 19C(1) in relation to a licence held by an importing licensee (whether in pursuance of section 15B(2) or otherwise), or

information on any appropriate control measures carried out by the Authority (whether in pursuance of section 15B(2) or otherwise).