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Source: Science, Dec 18, 1998 v282 i5397 p2194(1).

Title: Biological Weapons Control.(inspection of suspected biological
weapons manufacturing sites)(Brief Article)
Author: Johannes Rath, Bernhard Jank, Thomas P. Monath, Lance K. Gordon,
Johannes Rath and Bernhard Jank

Full Text COPYRIGHT 1998 American Association for the Advancement of Science

Letter writers discuss whether on-site inspections in biological weapons control are necessary and, if so, how they should be conducted. The concept of treating Alzheimer patients as regressed toward infancy is questioned: "Each Alzheimer patient has a lifetime of experiences that determines their unique set of human qualities ..." The use of chimpanzees in AIDS vaccine trials is debated. And the production of hydrogen in basalt aquifers is explored.

The current negotiations in Geneva to develop a legally binding instrument to strengthen the 1972 Biological and Toxin Weapons Convention (BTWC) are likely to result in an international declaration and inspection regime. This regime could have implications for both academic and industrial research, development, and production sites.

In a recent Policy Forum (Science's Compass, 20 Nov., p. 1423), Thomas P. Monath and Lance K. Gordon express their concerns about on-site inspections in biological weapons control, concluding with support of the concept and leaning toward on-site inspections with sampling at the site triggered by national "intelligence-gathering activities."

At an international symposium held at the Institute for Applied Microbiology, Vienna, Austria, in May 1998, the value of on-site inspections and sampling in a possible future biological weapons control regime was also addressed. The participants came from varied backgrounds: regulatory affairs and biosafety managers from industry and academia, diplomats, weapons inspectors, and representatives of various international and national authorities. They concluded that triggering inspections through suspicion could very likely stigmatize any of the inspected institutions.

In principal, a biological weapons control regime includes auditing, which presents the possibility of certifying that the site is compliant with the agreements on production, stockpiling, and use of biological weapons. If sites that possess dual use capabilities are inspected at random intervals, the inspection itself would leave no stigma; on the contrary, the outcome of the inspection could increase the level of confidence that the institution is complying with international agreements. This could reduce the need for restrictions in the international exchange of dual-use material, equipment, and know-how, a fear expressed at the symposium.

The delegates suggested that, to minimize the extra workload, a future protocol should take into account existing control regimes. For biopharmaceutical industries, in particular, consideration should be given to how the new protocol could be implemented nationally through use of existing infrastructures, such as those established under health and safety legislation.

Johannes Rath

Institut fur Zoologie, Universtat Wien, Althanstrasse 14, 1090 Vienna, Austria. E-mail: johannes.rath@univie.ac.at

Bernhard Jank

Otto Doblhoff-Dier

Institut fur Appl. Microbiol. Universitat Agric., Nussdorfer Laende 11, A-1190 Vienna, Austria. Email: dobihoff@edv2.boku.ac.at

Response

As Rath, Jank, and Doblhoff-Dier correctly point out, there is considerable debate about the pros and cons of an inspection regime as a means of enforcing the ban on biological weapons. We would like to correct one apparent misinterpretation of our position, with respect to triggers for visits. We do not suggest that the selection of facilities for inspection would be based principally on "intelligence-gathering activities." Rather, it is anticipated that the content of declarations submitted by states or parties containing information about activities at research and production sites, specific biological agents, biological weapons defensive research, aerosol studies, containment level, and so forth will be the basis for visits. A system for right of entry to declared sites is needed to increase transparency and reduce suspicions. The declaration process has revealed, and will continue to reveal questions that can be clarified most effectively by on-site visits. Serious concerns about potential violations can be resolved only by challenge inspections, which would be conducted at very short notice and would be based on information sufficient to pass stringent criteria. Without challenge inspections and the possibility of on-site analysis, the treaty would remain a "dog without teeth." It is likely that those states engaged in offensive biological research and development will continue to deceive the international community and that illegal activities will be carried out at undeclared facilities. Ultimately, intelligence gathering may be useful in revealing such facilities and bringing them under the scrutiny of the inspectorate. It is our expectation, however, that some states or parties may decide that it is not worth the political and economic risk to initiate (or continue) offensive programs. The threat of enforcement of the Chemical Weapons Treaty resulted in the declaration and abandonment of previously denied programs.

We do not share the same apprehension expressed by participants at the Vienna conference with respect to the stigma attached to visits and inspections. Intrusive visits by various regulators are already frequent occurrences, and once biological weapons visits become regular events, they will hardly be "news." We also do not share the view that the fox should guard the henhouse; self-enforcement through national legislation does not provide a reasonable safeguard against state-sponsored biological weapons programs

Thomas P. Monath

Lance K. Gordon

OraVax Inc., 38 Sidney Street, Cambridge, MA 02139, USA. E-mail: tmonath@oravax.com

 
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