Assisted Human Reproduction (Section 8 Consent) Regulations (SOR/2007-137)

Regulations are current to 2014-07-22 and last amended on 2007-12-01. Previous Versions

Assisted Human Reproduction (Section 8 Consent) Regulations

SOR/2007-137

ASSISTED HUMAN REPRODUCTION ACT

Registration 2007-06-14

Assisted Human Reproduction (Section 8 Consent) Regulations

P.C. 2007-958 2007-06-14

Her Excellency the Governor General in Council, on the recommendation of the Minister of Health, pursuant to subsection 65(1) of the Assisted Human Reproduction ActFootnote a, hereby makes the annexed Assisted Human Reproduction (Section 8 Consent) Regulations.

INTERPRETATION

  •  (1) The following definitions apply in these Regulations.

    “Act”

    “Act” means the Assisted Human Reproduction Act. (Loi)

    “common-law partner”

    “common-law partner”, in relation to an individual, means a person who is cohabiting with the individual in a conjugal relationship at the relevant time, having so cohabited for a period of at least one year. (conjoint de fait)

    “third party”

    “third party” means

    • (a) in relation to human reproductive material,

      • (i) an individual who is not the donor of the human reproductive material or the spouse or common-law partner of that donor, or

      • (ii) a couple in respect of whom neither spouse or common-law partner is the donor of the human reproductive material; and

    • (b) in relation to an in vitro embryo,

      • (i) an individual who is not the donor of the in vitro embryo under subsection 10(1), or

      • (ii) a couple who is not the donor of the in vitro embryo under subsection 10(1). (tiers)

  • (2) In these Regulations, the term “spouse” does not include a person who, at the relevant time, lives separate and apart from the person to whom they are married because of the breakdown of their marriage.

  • (3) For the purpose of these Regulations, the written consent of a donor must be signed by the donor and attested by a witness.

PART 1CONSENT GIVEN UNDER SUBSECTION 8(1) OF THE ACT

 This Part applies in respect of a consent given under subsection 8(1) of the Act to make use of human reproductive material for the purpose of creating an embryo.

 Before a person makes use of human reproductive material for the purpose of creating an embryo, the person shall have a document signed by the donor of the material stating that, before consenting to the use of the material, the donor was informed in writing that

  • (a) subject to paragraph (b), the human reproductive material will be used in accordance with the donor’s consent to create an embryo for one or more of the following purposes, namely,

    • (i) the donor’s own reproductive use,

    • (ii) following the donor’s death, the reproductive use of the person who is, at the time of the donor’s death, the donor’s spouse or common-law partner,

    • (iii) the reproductive use of a third party,

    • (iv) improving assisted reproduction procedures, or

    • (v) providing instruction in assisted reproduction procedures;

  • (b) if the human reproductive material is to be removed from the donor’s body after the donor’s death, the material will be used in accordance with the donor’s consent to create an embryo for one or more of the following purposes, namely,

    • (i) the reproductive use of the person who is, at the time of the donor’s death, the donor’s spouse or common-law partner,

    • (ii) improving assisted reproduction procedures, or

    • (iii) providing instruction in assisted reproduction procedures;

  • (c) if the donor wishes to withdraw their consent, the withdrawal must be in writing;

  • (d) the withdrawal is effective only if the person who intends to make use of the human reproductive material is notified in writing of the withdrawal

    • (i) in the case of human reproductive material to be used to create an embryo for a purpose mentioned in paragraph (a) or (b), other than subparagraph (a)(iii), before the material is used, and

    • (ii) in the case of human reproductive material to be used to create an embryo for the purpose mentioned in subparagraph (a)(iii), before the third party acknowledges in writing that the material has been designated for their reproductive use;

  • (e) the number of in vitro embryos created with the human reproductive material may be in excess of the immediate reproductive needs of the individual or couple for whom they were created;

  • (f) if the human reproductive material is used to create in vitro embryos for a third party’s reproductive use and there are in vitro embryos in excess of the third party’s reproductive needs, the excess in vitro embryos will be used in accordance with the third party’s consent and, if the use is providing instruction in assisted reproduction procedures, improving assisted reproduction procedures or other research, the consent of the donor in accordance with section 4;

  • (g) if the human reproductive material is used to create in vitro embryos for the reproductive use of the person who, at the time of the donor’s death, is the donor’s spouse or common-law partner and there are in vitro embryos in excess of the spouse or common-law partner’s reproductive needs, the excess in vitro embryos will be used in accordance with the spouse or common-law partner’s consent and, if the use is providing instruction in assisted reproduction procedures, improving assisted reproduction procedures or other research, the consent of the donor in accordance with section 4;

  • (h) if the human reproductive material is used to create in vitro embryos for the reproductive use of a third party who is a couple, along with human reproductive material from an individual who is a spouse or common law partner in the couple, the use of the in vitro embryos will be subject to the consent of that individual alone if, prior to the use of the in vitro embryos, the individual is no longer a spouse or common-law partner in the couple; and

  • (i) if the donor consents to the human reproductive material being used to create an in vitro embryo for the purpose of providing instruction in assisted reproduction procedures or improving assisted reproduction procedures, no additional consent from the donor is required to permit the use of the embryo for that purpose.