The following HTML text is provided to enhance online
readability. Many aspects of typography translate only awkwardly to HTML.
Please use the page image
as the authoritative form to ensure accuracy.
U.S. Food and Drug Administration (FDA). 1993. Application of current statutory authorities to human somatic cell therapy products and gene therapy products. Federal Register Notice, October 14.
Walters, J. 1995. Presentation to the IOM Conference on Xenograft Transplantation: Science, Ethics, and Public Policy. June 25-27.
