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The Journal of Biolaw & Business|March 17, 2006
International stem cell use and regulation in researchLaura Lin
The Journal of Biolaw & Business|November 23, 2006
Research examines the minimal risk standard for pediatric researchArlene D Luu
The Journal of Biolaw & Business|December 13, 2006
Good clinical practice (GCP) standards: clinical trials in India. An interview with Dr. Urmila Thatte, Head of Clinical Pharmacology, TN Medical College & BYL Nair Hospital. Interview by Viveka RoychowdhuryUrmila Thatte
The Journal of Biolaw & Business|May 20, 2003
Clinical trials face heightened scrutiny as science and commerce appear to mergeAlvin J Lorman
The Journal of Biolaw & Business|May 20, 2003
Mapping of human genome raises serious issues for individual vs. corporate rightsJ Court
The Journal of Biolaw & Business|May 20, 2003
Pharmaceutical advertising as a consumer empowerment deviceP H Rubin
The Journal of Biolaw & Business|October 6, 2004
Understanding orphan drug regulations: an EU and U.S. comparative analysisAurelie Grienenberger
The Journal of Biolaw & Business|July 9, 2004
A physician's duty to warn family members of genetic risks: limiting the importance of TarasoffScott Russell
The Journal of Biolaw & Business|July 17, 2004
Gene therapy, fundamental rights, and the mandates of public healthJohn Lynch
The Journal of Biolaw & Business|April 10, 2004
Sponsored research agreements, university and government licensing, and clinical trial agreements: special contractual and intellectual property rights considerationsJeffrey P Somers
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