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» Introduction
» Ethical Issues?
» Politics of Cloning
» Bill C-56 and Bill C-13
» Current AHR Regulation
» Summary of Bill C-13
» Reaction to Bill C-13
» The Future of Bill C-13
 
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External Info & Links
« Bill C-13: Full Text
« Bill C-47: Full Text
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The Politics of Genetic and Reproductive Technologies
Canada’s efforts to legislate the AHR field date back to the late 1980s

In Canada, efforts to provide a legislative and regulatory framework for assisted human reproductive technologies date back to the late 1980s:

  • In 1989, the government set up the Royal Commission on New Reproductive Technologies.
  • In 1993, the Royal Commission released its report, “Proceed with Care,” criticizing the state of reproductive technology in Canada. The report noted that some commercial clinics were allowing parents to choose the sex of their child, and sperm donor clinics were not always testing donors for diseases such as HIV.
  • The report stressed the need for federal legislation to safeguard the interests and protect the health of all the individuals involved in assisted human reproduction.
  • Two important recommendations involved banning research in several new technologies and establishing a regulatory agency

The Federal Government’s Response – Bill C-47

In 1995, the federal government imposed a voluntary moratorium on nine controversial technologies, including the commercialization of eggs and sperm, stem cell research on human embryos, and human cloning. Groups engaged in these activities wouldn’t receive federal funding.

In 1996, Based on the Royal Commission’s report, the federal government introduced Bill C-47, the Human Reproductive and Genetic Technologies Act. The legislation continued the ban on nine technologies contained in the voluntary moratorium, and added others.

Bill C-47 made it through first reading, but died on the order paper after the Liberals called a federal election in Spring 1997. Even so, it is not clear that the bill would have otherwise passed. Stakeholders such as scientists and infertility clinic operators found several flaws with the legislation:

  • It took an overly negative view of reproductive technologies. The bill’s sole purpose was to prohibit several procedures, not to indicate what should be allowed.
  • It didn’t take into account new technologies – such as the ability to detect genetic diseases at the embryonic stage - that were being developed. Modifying the bill at a later date to take these new technologies into account would have been extremely difficult.
  • It made no effort to ensure activities that weren’t prohibited were carried out under specific prescribed conditions.
  • It made no effort to distinguish between offenses when assigning penalties.

Dolly the Sheep - A New Era in Genetic Research

In July 1996, Scottish scientists made headlines when they announced that they had produced the world’s first cloned mammal, a sheep named Dolly. What made Dolly’s birth significant is that she was cloned with DNA taken from an adult cell. Scientists predicted that a similar method could soon be used to clone humans. (While receiving less publicity at the time, the event also held enormous potential for farmers, since the possibility now existed to clone adult animals whose characteristics - such as level of milk production - were already known). Since 1996, dairy cows, goats, and pigs have been successfully cloned.

Following Dolly’s birth, US President Clinton passed legislation banning the use of federal funding for human cloning experiments. In Canada, Bloq Québécois (BQ) MP Pauline Picard introduced a private member’s bill (Bill C-247) in 1999, criminalizing all cloning of human embryos. Although the bill’s overriding intent was to prevent human reproductive cloning, it would have also criminalized therapeutic cloning and genetic manipulation of human cells.

Bill C-247 failed to get past first reading. The House of Commons Standing Committee on Health decided more comprehensive legislation was required, and withdrew the bill. Meanwhile, the government entered into discussions with the medical community to develop legislation that would prohibit certain procedures, while remaining flexible enough to assess newly developing technologies as they became available. The government also wanted to establish a regulatory agency to monitor and enforce the Act.

Next Page >>
Canada Tries Again: Bill C-56 and Bill C-13


 

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