Assisted Human Reproduction Act
Marginal note:Information to be collected by licensees
14 (1) A licensee shall not accept the donation of human reproductive material or an in vitro embryo from any person for the purpose of a controlled activity, and shall not perform a controlled activity on any person, unless the licensee has obtained from that person the health reporting information required to be collected under the regulations.
Marginal note:Requirements of this Act to be conveyed
(2) Before accepting a donation of human reproductive material or of an in vitro embryo from a person or accepting health reporting information respecting a person, a licensee shall
(a) inform the person in writing of the requirements of this Act respecting, as the case may be,
(i) the retention, use, provision to other persons and destruction of the human reproductive material or in vitro embryo, or
(ii) the retention, use, disclosure and destruction of the health reporting information;
(b) to the extent required by the regulations, make counselling services available to the person and ensure that the person receives them;
(c) obtain the written consent of the person to the application of the requirements referred to in paragraph (a); and
(d) in accordance with the regulations, provide the person with the information that the Agency makes available to the public under paragraph 19(i).
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