§5601. Purposes
The purposes of this chapter are-
(1) to mandate United States sanctions, and to encourage international sanctions, against countries that use chemical or biological weapons in violation of international law or use lethal chemical or biological weapons against their own nationals, and to impose sanctions against companies that aid in the proliferation of chemical and biological weapons;
(2) to support multilaterally coordinated efforts to control the proliferation of chemical and biological weapons;
(3) to urge continued close cooperation with the Australia Group and cooperation with other supplier nations to devise ever more effective controls on the transfer of materials, equipment, and technology applicable to chemical or biological weapons production; and
(4) to require Presidential reports on efforts that threaten United States interests or regional stability by Iran, Iraq, Syria, Libya, and others to acquire the materials and technology to develop, produce, stockpile, deliver, transfer, or use chemical or biological weapons.
(
Editorial Notes
References in Text
This chapter, referred to in text, was in the original "this title", meaning title III of
Statutory Notes and Related Subsidiaries
Short Title
Matters Relating to the Control of Biological Weapons
"SEC. 1121. SHORT TITLE.
"This chapter may be cited as the 'National Security and Corporate Fairness under the Biological Weapons Convention Act'.
"SEC. 1122. DEFINITIONS.
"In this chapter:
"(1)
"(2)
"(3)
"SEC. 1123. FINDINGS.
"Congress makes the following findings:
"(1) The threat of biological weapons and their proliferation is one of the greatest national security threats facing the United States.
"(2) The threat of biological weapons and materials represents a serious and increasing danger to people around the world.
"(3) Biological weapons are relatively inexpensive to produce, can be made with readily available expertise and equipment, do not require much space to make and can therefore be readily concealed, do not require unusual raw materials or materials not readily available for legitimate purposes, do not require the maintenance of stockpiles, or can be delivered with low-technology mechanisms, and can effect widespread casualties even in small quantities.
"(4) Unlike other weapons of mass destruction, biological materials capable of use as weapons can occur naturally in the environment and are also used for medicinal or other beneficial purposes.
"(5) Biological weapons are morally reprehensible, prompting the United States Government to halt its offensive biological weapons program in 1969, subsequently destroy its entire biological weapons arsenal, and maintain henceforth only a robust defensive capacity.
"(6) The Senate gave its advice and consent to ratification of the Biological Weapons Convention in 1974.
"(7) The Director of the Arms Control and Disarmament Agency explained, at the time of the Senate's consideration of the Biological Weapons Convention, that the treaty contained no verification provisions because verification would be 'difficult'.
"(8) A compliance protocol has now been proposed to strengthen the 1972 Biological Weapons Convention.
"(9) The resources needed to produce, stockpile, and store biological weapons are the same as those used in peaceful industry facilities to discover, develop, and produce medicines.
"(10) The raw materials of biological agents are difficult to use as an indicator of an offensive military program because the same materials occur in nature or can be used to produce a wide variety of products.
"(11) Some biological products are genetically manipulated to develop new commercial products, optimizing production and ensuring the integrity of the product, making it difficult to distinguish between legitimate commercial activities and offensive military activities.
"(12) Only a small culture of a biological agent and some growth medium are needed to produce a large amount of biological agents with the potential for offensive purposes.
"(13) The United States pharmaceutical and biotechnology industries are a national asset and resource that contribute to the health and well-being of the American public as well as citizens around the world.
"(14) One bacterium strain can represent a large proportion of a company's investment in a pharmaceutical product and thus its potential loss during an arms control monitoring activity could conceivably be worth billions of dollars.
"(15) Biological products contain proprietary genetic information.
"(16) The proposed compliance regime for the Biological Weapons Convention entails new data reporting and investigation requirements for industry.
"(17) A compliance regime which contributes to the control of biological weapons and materials must have a reasonable chance of success in reducing the risk of production, stockpiling, or use of biological weapons while protecting the reputations, intellectual property, and confidential business information of legitimate companies.
"SEC. 1124. TRIAL INVESTIGATIONS AND TRIAL VISITS.
"(a)
"(b)
"(c)
"(1) in each trial investigation or trial visit conducted pursuant to subsection (a); and
"(2) in each trial investigation or trial visit conducted pursuant to subsection (b), except for any investigation or visit in which the host facility requests that such personnel not participate,
for the purpose of assessing the information security implications of such investigation or visit. The Secretary of Defense, in coordination with the Director of the Federal Bureau of Investigation, shall add to the report required by subsection (d)(2) a classified annex containing an assessment of the risk to proprietary and classified information posed by any investigation or visit procedures in the compliance protocol.
"(d)
"(1)
"(A) an assessment of risks to national security and United States industry and research institutions of such on-site activities; and
"(B) an assessment of the monitoring results that can be expected from such investigations and visits.
"(2)
"(A) the findings of the study conducted pursuant to paragraph (1); and
"(B) the results of trial investigations and trial visits conducted pursuant to subsections (a) and (b)."