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References - Requests for Human Biological Materials

NIH Clinical Center. Policy and Communications Bulletin. Medical Administrative Series. M01-2 (rev). SUBJECT: Procurement and Use of Human Biological Materials for Research. April 22, 2001.

NIH Clinical Center. Policy and Communications Bulletin. Medical Administrative Series. M77-2 (rev.). SUBJECT: Informed Consent. May 30, 2001.

NIH Clinical Center. POLICY: Guidelines for Blood Drawn for Research Purposes in the Clinical Center. October 1, 1995.

Code of Federal Regulations. Title 42, Public Health, Chapter IV - Health Care Financing Administration, Department of Health and Human Services, Part 493:  Laboratory Requirements, Revised, October 1, 2000.

Code of Federal Regulations. Title 45, Public Welfare, Department of Health and Human Services, National Institutes of Health, Office for Protection from Research Risks, Part 46: Protection of Human Subjects. Revised, June 18, 1991. Effective August 19, 1991.

Code of Federal Regulations. Title 45, Standards for Privacy of Individually Identifiable Health Information, Final Rule Parts 160 and 164. (Implementation of Health Insurance Portability and Accountability Act of 1996) Final Rule, December 28, 2000. Effective April 14, 2001.

H.R. 3569. Human Research Protection and Promotion Act of 2000 (Introduced in the House, February 2, 2000 and referred to the Subcommittee on Health and Environment, February 7, 2000).

NCI. Confidentiality, Data Security, and Cancer Research: Perspectives from the National Cancer Institute. March 23, 1999.

NCI. Uses of Human Tissues. August 28, 1996.

The National Commission for the Protection of Human Subjects. The Belmont Report, Office of the Secretary. Ethical Principles and Guidelines for the Protection of Human Subjects Research. April 18, 1979.

The Warren Grant Magnuson Clinical Center. The Medical Record Handbook. October, 2000.

Return to Requests for Human Biological Materials

Last updated by Chinquee, Joseph (NIH/NCI) [E] on Feb 16, 2017