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Emerging Regulatory Issues for Human Stem Cell Medicine1

  • Kathleen Liddell
  • Susan Wallace
Open Access
Article

Abstract

The regulation of stem cell research is an issue that has drawn much comment, criticism and even judicial arbitration in recent years. An emerging issue, addressed in this article, is how the fruits of that research-stem cell medicine-are likely to be regulated en route from lab to market. Taking account of the ethical, legal, social and safety issues raised by stem cell medicine and the goals of governance, the article explains the relevant regulatory instruments (e.g. the draft UK Stem Cell Bank Code, the EU Directive on Human Tissue, the EU Directives on medical products and devices, and the Human Tissue Act 2004) and critically examines the framework they provide.

Keywords

Stem Cell Human Tissue Safety Issue Medical Product Stem Cell Research 
These keywords were added by machine and not by the authors. This process is experimental and the keywords may be updated as the learning algorithm improves.

Notes

Copyright information

© ESRC Genomics Network 2005

Authors and Affiliations

  • Kathleen Liddell
  • Susan Wallace

There are no affiliations available

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