USE OF HUMAN SUBJECTS

• Document Type: CREST
• Collection: STARGATE
• Document Number (FOIA) /ESDN (CREST): CIA-RDP96-00789R003000420008-5
• Release Decision: RIFPUB
• Original Classification: U
• Document Page Count: 2
• Document Creation Date: November 4, 2016
• Document Release Date: December 7, 1998
• Sequence Number: 8
• Publication Date: July 7, 1991
• Content Type: REGULATION

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USE OF HUMAN SUBJECTS
A. Definition
Human Subject: An individual about whom an investigator conducting research obtains data through
interaction with the individual, including both physical procedures and manipulations of the subject or
the subject's environment. The term does not include personnel of any type who are quali5ed to test by
assignment to duties that call specifically for such qualifications (e.g., test engineers).
B. General Guidance
1. The contractor shall conduct research using human subjects at all times so as to be in full compliance
with all applicable laws and federal regulations. Among them are:
? 45 CFR 46 Health and Human Services (HHS) Regulations "Protection of Human Subjects."
i 10 U. S. C. Section 980, "Limitations on Use of Humans as Experimental Subjects."
2. Safeguarding the rights and welfare of subjects at risk in activities supported by this contract is the
responsibility of the Contractor. Compliance with this contract will in no way render. inapplicable
pertinent federal, state, or local laws or regulations. In order to provide for the adequate discharge
of this institutional responsibility, no activity involving human subjects under this contract shall be
undertaken unless a Contractor Human Use Review Board (CRB) has reviewed and approved such
activity.
3. 'T'he contractor must provide the Contracting Officer with a written assurance that it is in com-
pliance with all provisions of 45 CFR 46 HHS Regulation, "Protection of Human Subjects," as
amended.
4. The Contractor will assure the Contracting Officer that the identities of all subjects wi11, be pro-
tected.
S. Informal consent must be obtained in writing from each human subject before research is undertak-
en.
6. The contractor shall provide all necessary medical care to research subjects for injury or disease
which is the proximate result of participation in the research.
7. Studies conducted outside the United States, its territories or possessions, shall be conducted in
compliance with all laws, customs, and practices of the country in which the study is to be conducted.
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C. Requirements for Reporting and Documentation
1. Copies of all documents presented or required for initial and, continuing review of the CRB (e.g.,
Board minutes pertaining only to the contract, record of subjects consent, transmittal on actions,
instructions and conditions resulting from Board deliberations addressed to the activity director)
are to be retained by the Contractor for at least three (3) years after completion of the research. All
documents shall be accessible for inspection during normal working hours by the sponsor's COTR or
authorized representative.
2. Except as otherwise provided by law, information in the records of possession of the Contractox
which refers to or can be identified with a particular subject may not be disclosed except:
a. With the consent of the subject or his legally authorized representative, or
b. As maybe necessary for the sponsor to carry out its legal responsibilities.
3. Upon expiration or termination of the contract, a list of all unused test material shall be provided to
the sponsor's Contracting Officer.
4. The Contractor shall immediately notify the sponsor's Contracting Officer, by telephone, of inqui-
ries from sources outside the government concerning the use of human subjects under this contract.
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