Reproductive medicine meets human embryonic stem cell (hESC) research: the need to adjust the regulatory framework to actual expectations and potential detrimental consequences of hESC research
Human embryonic stem cell (hESC)-based cell therapy depends on access to surplus embryos from IVF cycles and collaborative interactions between biomedical researchers and reproductive medicine professionals. It is becoming instrumental to achieve an international consensus about the standards that should regulate the manipulation of human embryonic tissue in two distinct settings: reproductive medicine and embryonic stem cell research. Within hESC research, the regulatory framework needs to be adjusted according to the actual expectations and potential detrimental consequences of hESC research.
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J.L.C. has nothing to disclose. P.M. has nothing to disclose.
Supported by the Consejería de Salud, Junta de Andalucía (grants reference 0029/2006 and 0030/2006), The International Jose Carreras Foundation Against Leukemia Award (EDThomas-05 to P.M.), and the Spanish Ministry of Health (FIS-PI070026 to P.M.).
PII: S0015-0282(08)01153-9
doi:10.1016/j.fertnstert.2008.05.041
© 2009 American Society for Reproductive Medicine. Published by Elsevier Inc. All rights reserved.

