Data protection: UK bill improved and approved

The Data Protection Bill, which provides individuals the right of access to computerized data about themselves while preventing unauthorized disclosure of information, passed Britain's House of Commons at its third reading and returned to the House of Lords. Among the amendments added to the controversial legislation was one concerning the transfer of medical information to agencies outside the health system. After extensive lobbying by the medical community, the government agreed that a code of practice governing disclosure of medical data recently developed by an interprofessional working group should apply in principle to computerized records.     

Human embryo research: INSERM to ponder ethics

France has established its first "national advisory committee on ethics for the life sciences and health research." The committee, to consist of 4 "moralists", 14 scientists, and 14 government representatives, will advise on issues posed by government ministries, organize annual public debates, and establish an international documentation and information center. The first issue on its agenda is a draft law on the use of fetal tissue for medical research.     

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