- And… We’re Back.
- Transitions
- Bioethical Marching Orders
- FDA Intervention Shelves Plan for Drugstore Genome Tests
- The Boons of an NIH Boost
- Crime Lab DNA Databases Under the Microscope
- Domes of Carbon Over U.S. Cities Damage Urban Health
- FDA Rules for Cigarettes Are a Victory for Public Health, for Science (and for the Earth’s Climate?)
- Legislation Introduced to Codify Stem Cell Rules
- Commissioner Enhances FDA’s Commitment to Personalized Medicine
- Perfecting Policy on Stem Cells
- NIH and FDA Aim to Retool Regulatory Science
- September 2010
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- September 2007
Legislation Introduced to Codify Stem Cell Rules
Last week, Rep. Diana DeGette (D-CO) introduced a bill that would codify the bedrock bioethical safeguards for federally-funded human embryonic stem cell research. These provisions reflect the guidelines that have been in effect at the National Institutes of Health since last July and also align with the guidelines that the Center for American Progress recommended in the January 2009 report “A Life Sciences Crucible.”
Specifically, the legislation ensures that the cells are procured from embryos that were created through in-vitro fertilization for reproductive therapy, were deemed in excess of the patient’s clinical need, and would otherwise be discarded. The patients must also provide informed consent and must not receive any financial inducements.
These provisions uphold basic values that protect the autonomy of embryo donors and grant special consideration to the moral status of the embryo while also fostering the advancement of scientific knowledge for the common good and the benefit of patients everywhere.
It is encouraging to see legislators championing the intellectually robust research standards that the bioethics community has consistently advocated over years of sincere and informed discussion on the science and ethics of stem cell research.
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