Long title | An Act to make provision in connection with human embryos and any subsequent development of such embryos; to prohibit certain practices in connection with embryos and gametes; to establish a Human Fertilisation and Embryology Authority; to make provision about the persons who in certain circumstances are to be treated in law as the parents of a child; and to amend the Surrogacy Arrangements Act 1985. |
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Citation | 1990 c. 37 |
Territorial extent | England, Northern Ireland, Scotland and Wales |
Dates | |
Royal assent | 1 November 1990 |
Status: Amended | |
Text of the Human Fertilisation and Embryology Act 1990 as in force today (including any amendments) within the United Kingdom, from legislation.gov.uk. |
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The Human Fertilisation and Embryology Act 1990 (c. 37) is an Act of the Parliament of the United Kingdom. It created the Human Fertilisation and Embryology Authority which is in charge of human embryo research, along with monitoring and licensing fertility clinics in the United Kingdom. [1]
The Authority is composed of a chairman, a deputy chairman, and however many members are appointed by the UK Secretary of State. They are in charge of reviewing information about human embryos and subsequent development, provision of treatment services, and activities governed by the Act of 1990. [1] The Authority also offers information and advice to people seeking treatment, and to those who have donated gametes or embryos for purposes or activities covered in the Act of 1990. Some of the subjects under the Human Fertilisation and Embryology Act of 1990 are prohibitions in connection with gametes, embryos, and germ cells. [2]
The Act also addresses licensing conditions, code of practice, and procedure of approval involving human embryos. [3] This only concerns human embryos which have reached the two cell zygote stage, at which they are considered "fertilised" in the act. [2] It also governs the keeping and using of human embryos, but only outside a woman's body. The act contains amendments to UK law regarding termination of pregnancy, surrogacy and parental rights. [2]
The Human Fertilization and Embryology Act 1990 regulates ex-vivo human embryo creation and the research involving them. This act established the Human Fertilisation and Embryology Authority (HFEA) to regulate treatment and research in the UK involving human embryos. In 2001, an extension of the Act legalized embryo research for the purposes of "increasing knowledge about the development of embryos," "increasing knowledge about serious disease," and "enabling any such knowledge to be applied in developing treatments for serious disease." The HFEA grants licenses and research permission for up to three years, based on approval of five steps by the Research License Committee. [4]
HFEA policies are reviewed by specialists in the field regularly. After research and literature are reviewed, and open public meetings are held, the summarized information is presented to the Human Fertilisation Embryology Authority. [4]
Donors must meet certain criteria in order to be eligible for sperm, egg, or embryo donation. The donor can donate for research purposes or fertility treatment. Donors should find a HFEA licensed clinic, or can go through the National Gamete Donation Trust. [5]
The HFEA is carrying out a detailed review to determine the best way to reduce the risk of multiple pregnancies with in vitro fertilization (IVF). For example, Nadya Suleman (or "Octomom") is publicly known for giving birth to octuplets after IVF treatment.
This policy allows for the use of techniques which alter the mitochondrial DNA of the egg or an embryo used in IVF, to prevent serious mitochondrial diseases from being inherited.
The policies reviewed by HFEA cover everything from human reproductive cloning to the creation of human-animal hybrids, and include subjects such as ethics with scientific and social significance.
Sperm, eggs and embryos received in the donation process are currently tested for many medical conditions, and also quarantined for six months to reduce the risk of complications to the mother and child. Other than a screening for genetic disorders, donors are tested for HIV, hepatitis B, and hepatitis C. [6]
Embryos must be donated by a woman between the ages of 18 and 35 years old, who has also undergone a medical screening and given informed consent (which can be revoked at any point up until the embryo is used). [6]
"Welfare of the Child" review (multiple pregnancy), for people seeking IVF treatment. While there is always a risk of having a multiples pregnancy after receiving IVF treatment, HFEA is reviewing policies which will reduce this dangerous possibility. No more than two eggs or embryos can be legally implanted in a woman in an IVF treatment. There is a 25% success rate of this procedure per treatment cycle. [6]
Includes safety procedure regulations at fertility clinics; includes safe cryopreservation of eggs and embryos. Eggs and embryos are stored for ten years after the initial treatment. If the patient decides not to pursue another pregnancy, the eggs and embryos can be donated for research or to another couple for fertility treatments. [6]
In donor-assisted conception, the donor may not receive any monetary compensation (in the UK), although they may have related expenses covered. [7]
Sperm, eggs and embryos are stored in liquid nitrogen using cryopreservation (defined as the freezing of cells or whole tissues to sub-zero temperatures—the boiling point of liquid nitrogen). [8] This method preserves living organisms in a state where they can be restored to how they were before freezing. [8]
A cryoprotective compound (a liquid called cryopreservation medium), along with carefully controlled cooling and warming cycles ensure that minimal damage is done to the cells. [9] [8]
However, the freezing process is still somewhat damaging. Therefore, men wishing to donate sperm or have it stored for future use must make six sperm deposits for every one child they wish to have, due to the 50% survival rate of the sperm in each deposit. [8] The sperm is then put into straw shaped vials, and placed in a storage tank of either liquid nitrogen, or liquid nitrogen vapor. The sub-zero temperatures of the liquid generally range from -150 degrees Celsius, to -196 degrees Celsius.
According to HFEA, the storage period for both human gametes and embryos cannot exceed ten years. [9] HFEA requires a full informed consent from each party that has any relation to the egg, gametes, or embryo, all of which must be stored in accordance with their consents. [9]
Exceptions to the informed consent of gamete storage:
The act states that it is legal to "take" gametes or accept those provided, and store them without a person's consent, if the person is considered incapable, or until they "acquire such capacity." [9]
However, under paragraphs 9 and 10 of HFEA 1990, a person's gametes cannot be legally stored in the UK after their death. [9]
In July 1982 the Warnock Committee Inquiry was established. It was "to consider recent and potential developments in medicine and science related to human fertilisation and embryology; to consider what policies and safeguards should be applied, including consideration of the social, ethical, and legal implications of these developments; and to make recommendations." [10]
The Warnock Report was published on 18 July 1984. The report stated that a regulator was needed due to the 'special status' of embryos. [10]
In 1985 the Interim Licensing Authority was created. It was supposed to regulate work and research regarding human in vitro fertilisation until a permanent government legislation was passed. It remained the only authority until 1990.
The Unborn Children Protection Bill was also created in 1985. It was written by Enoch Powell and prohibited embryonic research. The Health Secretary would only have been allowed an embryo to be kept and implanted if it was for the sole purpose of assisting a named woman to bear a child. No other reason was allowed. This bill was not passed. It was reintroduced in 1986, where it again failed to pass. This was repeated again 1989. [10]
The Surrogacy Arrangements Act 1985 was the first law that governed surrogacy arrangements. It criminalized commercial surrogacy arrangements. [10]
In 1987 the framework for human fertilisation and embryology was created. A white paper was published in regards to the recommendations of the Warnock Report. [10]
In 1990 the Human Fertilisation and Embryology Act 1990 was passed. The Human Fertilisation and Embryology Authority, HFEA, officially started work August 1, 1991. [10]
The act covers several areas:
Within the act an embryo is defined as a live human embryo where fertilisation is complete, complete is defined as the appearance of a two cell zygote.
The act states that eggs, sperm, and embryo can only be stored for a finite amount of time in very specific conditions that are regulated by the Human Fertilisation and Embryology Authority. [11]
Research on human embryos can only be performed for specifically defined purposes that must be considered 'necessary and desirable' by the Human Fertilisation and Embryology Authority. Research can only be performed on an embryo for a maximum of fourteen days or until the primitive streak appears. The genetic composition of any cell within the embryo cannot be altered during the embryo's formation for research. [11]
The act defined several purposes: [3]
Section 37 [12] of the Act amends the Abortion Act 1967. The section specifies and broadens the conditions where abortion is legal.
Women who consider abortion are referred to two doctors. Each doctor then advises her whether abortion is a suitable decision based on the conditions listed below. An abortion is granted only when the doctors reach a unanimous decision that the woman may terminate her pregnancy. An abortion that is performed without this decision or under any other circumstances is considered unlawful.
Abortion may be granted under one of the following circumstances: [12]
- if the pregnancy has not exceeded its 24th week (previously lowered from 28 weeks in the Abortion Act of 1967) and has a heightened risk of injury to the physical and/or mental health of the mother, existing children, or family
- if the pregnancy places the mother's life in jeopardy
- if the pregnancy poses a risk of grave permanent injury to the mental or physical health of the mother
- if there is significant risk or evidence that the unborn child would suffer from physical or mental abnormalities, resulting in a serious handicap
The registered medical practitioner that performs the abortion will continue to act in accordance with the Infant Life (Preservation) Act 1929. [12]
In 1991 the statutory storage period and special expeditions sections were revisited. Regulations were extended storage periods for eggs and sperm. Licensing rules for egg and sperm storage were also clarified. [10]
A Disclosure of Information Act was created in 1992. This allowed the Human Fertilisation and Embryology Authority to disclose information to others with the patient's consent. for example, information could be shared with their general practitioner.
The Criminal Justice and Public Order Act 1994 added section 156. This prohibited the treatment of cells from aborted embryos. During the same year the Parental Orders regulations allowed parental orders to be made in surrogacy cases. [10]
In 1996 the permitted storage period for embryos was extended.
The Human Fertilisation and Embryology (Deceased Fathers) Act 2003 amended section 28 in 2000. [13]
Sperm may be taken from a deceased male to fertilize an egg if the corresponding man and woman were:
In 2001 the Human Fertilisation and Embryology Regulations were added. These regulations extended the purposes that an embryo can be created for in regards to research. [11]
In addition, the Human Reproductive Cloning Act 2001 was passed. This essential made human reproductive cloning illegal by outlawing the implantation of research embryos.
As of 2004 the Disclosure of Donor Information Regulations were formed. Any sperm or egg donors registered after April 1, 2005, were required to pass on name and last address given to the offspring. [10] During this time Parliament began reviewing the Human Fertilisation and Embryology Act 1990. [14]
Licensing of all establishments handling gametes for treatment was required as of 2007 in the Quality and Safety Regulations.
In 2006 a white paper was published regarding a revised legislation for fertility. This led to the Human Fertilisation and Embryology Act 2008, HFE, being passed. This was a major review of fertility legislation, updating and amending the act of 1990. In 2009 the HFE act was passed. This is the current law in the UK. [10]
In vitro fertilisation (IVF) is a process of fertilisation in which an egg is combined with sperm in vitro. The process involves monitoring and stimulating a woman's ovulatory process, then removing an ovum or ova from her ovaries and enabling a man's sperm to fertilise them in a culture medium in a laboratory. After a fertilised egg (zygote) undergoes embryo culture for 2–6 days, it is transferred by catheter into the uterus, with the intention of establishing a successful pregnancy.
The Human Fertilisation and Embryology Authority (HFEA) is an executive non-departmental public body of the Department of Health and Social Care in the United Kingdom. It is a statutory body that regulates and inspects all clinics in the United Kingdom providing in vitro fertilisation (IVF), artificial insemination and the storage of human eggs, sperm or embryos. It also regulates human embryo research.
Assisted reproductive technology (ART) includes medical procedures used primarily to address infertility. This subject involves procedures such as in vitro fertilization (IVF), intracytoplasmic sperm injection (ICSI), cryopreservation of gametes or embryos, and/or the use of fertility medication. When used to address infertility, ART may also be referred to as fertility treatment. ART mainly belongs to the field of reproductive endocrinology and infertility. Some forms of ART may be used with regard to fertile couples for genetic purpose. ART may also be used in surrogacy arrangements, although not all surrogacy arrangements involve ART. The existence of sterility will not always require ART to be the first option to consider, as there are occasions when its cause is a mild disorder that can be solved with more conventional treatments or with behaviors based on promoting health and reproductive habits.
Embryo donation is one disposition option for users of in vitro fertilisation with remaining fresh or frozen embryos. It is defined as the giving—generally without compensation—of embryos remaining after in vitro fertilization procedures to recipients for procreative implantation or research. Most IVF users with supernumerary embryos make embryo donation decisions after completing their families or discontinuing use of in vitro fertilization. Recipients of embryos donated for procreative implantation typically plan to transfer fresh or frozen embryos into a prepared uterus in order to facilitate pregnancy and childbirth. Recipients of embryos donated for research typically use them for clinical training, quality improvement research, or human embryonic stem cell research.
Third-party reproduction or donor-assisted reproduction is any human reproduction in which DNA or gestation is provided by a third party or donor other than the one or two parents who will raise the resulting child. This goes beyond the traditional father–mother model, and the third party's involvement is limited to the reproductive process and does not extend into the raising of the child. Third-party reproduction is used by couples unable to reproduce by traditional means, by same-sex couples, and by men and women without a partner. Where donor gametes are provided by a donor, the donor will be a biological parent of the resulting child, but in third party reproduction, he or she will not be the caring parent.
A sperm bank, semen bank, or cryobank is a facility or enterprise which purchases, stores and sells human semen. The semen is produced and sold by men who are known as sperm donors. The sperm is purchased by or for other persons for the purpose of achieving a pregnancy or pregnancies other than by a sexual partner. Sperm sold by a sperm donor is known as donor sperm.
The British Pregnancy Advisory Service (BPAS) is a British charity whose stated purpose is to avoid unwanted pregnancy by advocating and providing high quality, affordable services to prevent or end unwanted pregnancies with contraception or by abortion.
Jane Denton,, is a United Kingdom nurse and midwife notable for her contributions to fertility nursing and genetics. She was made a Fellow of the Royal College of Nursing in 2006.
The hamster zona-free ovum test, or hamster egg-penetration test, or sometimes just hamster test, is an in-vitro test used to study physiological profile of spermatozoa. The primary application of the test is to diagnose male infertility caused by sperm unable to penetrate the ova. The test has limited value, due to expense and a high false negative rate.
Oocyte cryopreservation is a procedure to preserve a woman's eggs (oocytes). This technique is often used to delay pregnancy. When pregnancy is desired, the eggs can be thawed, fertilized, and transferred to the uterus as embryos. Several studies have shown that most infertility problems are due to germ cell deterioration related to aging. The procedure's success rate varies depending on the woman's age, health, and genetic factors. The first human birth of oocyte cryopreservation was reported in 1986.
Donor registration facilitates donor conceived people, sperm donors and egg donors to establish contact with genetic kindred. Registries are mostly used by donor conceived people to find out their genetic heritage and to find half-siblings from the same egg or sperm donor. In some jurisdictions donor registration is compulsory, while in others it is voluntary; but most jurisdictions do not have any registration system.
Sperm donation laws vary by country. Most countries have laws to cover sperm donations which, for example, place limits on how many children a sperm donor may give rise to, or which limit or prohibit the use of donor semen after the donor has died, or payment to sperm donors. Other laws may restrict use of donor sperm for in vitro fertilisation (IVF) treatment, which may itself be banned or restricted in some way, such as to married heterosexual couples, banning such treatment to single women or lesbian couples. Donated sperm may be used for insemination or as part of IVF treatment. Notwithstanding such laws, informal and private sperm donations take place, which are largely unregulated.
Fertility tourism is the practice of traveling to another country or jurisdiction for fertility treatment, and may be regarded as a form of medical tourism. A person who can become pregnant is considered to have fertility issues if they are unable to have a clinical pregnancy after 12 months of unprotected intercourse. Infertility, or the inability to get pregnant, affects about 8-12% of couples looking to conceive or 186 million people globally. In some places, rates of infertility surpass the global average and can go up to 30% depending on the country. Areas with lack of resources, such as assisted reproductive technologies (ARTs), tend to correlate with the highest rates of infertility.
Sperm donation is the provision by a man of his sperm with the intention that it be used in the artificial insemination or other "fertility treatment" of one or more women who are not his sexual partners in order that they may become pregnant by him. Where pregnancies go to full term, the sperm donor will be the biological father of every baby born from his donations. The man is known as a sperm donor and the sperm he provides is known as "donor sperm" because the intention is that the man will give up all legal rights to any child produced from his sperm, and will not be the legal father. Sperm donation may also be known as "semen donation".
Religious response to assisted reproductive technology deals with the new challenges for traditional social and religious communities raised by modern assisted reproductive technology. Because many religious communities have strong opinions and religious legislation regarding marriage, sex and reproduction, modern fertility technology has forced religions to respond.
The Human Fertilisation and Embryology Act 2008 is an act of the Parliament of the United Kingdom. The Act constitutes a major review and update of the Human Fertilisation and Embryology Act 1990.
Mitochondrial replacement therapy (MRT), sometimes called mitochondrial donation, is the replacement of mitochondria in one or more cells to prevent or ameliorate disease. MRT originated as a special form of in vitro fertilisation in which some or all of the future baby's mitochondrial DNA (mtDNA) comes from a third party. This technique is used in cases when mothers carry genes for mitochondrial diseases. The therapy is approved for use in the United Kingdom. A second application is to use autologous mitochondria to replace mitochondria in damaged tissue to restore the tissue to a functional state. This has been used in clinical research in the United States to treat cardiac-compromised newborns.
Cryopreservation of embryos is the process of preserving an embryo at sub-zero temperatures, generally at an embryogenesis stage corresponding to pre-implantation, that is, from fertilisation to the blastocyst stage.
Partner-assisted reproduction, reception of oocytes from partner (ROPA), reciprocal IVF,shared motherhood, partner IVF or co-IVF is a method of family building that is used by couples who both possess female reproductive organs. The method uses in vitro fertilization (IVF), a method that means eggs are removed from the ovaries, fertilized in a laboratory, and then one or more of the resulting embryos are placed in the uterus to hopefully create a pregnancy. Reciprocal IVF differs from standard IVF in that two partners are involved: the eggs are taken from one partner, and the other partner carries the pregnancy. In this way, the process is mechanically identical to IVF with egg donation. Reciprocal IVF offers the highest chance for pregnancy and a lower chance of a multiple births.
Lesbian, gay, bisexual, and transgender people people wishing to have children may use assisted reproductive technology. In recent decades, developmental biologists have been researching and developing techniques to facilitate same-sex reproduction.