Published 1993 by NABC.

In May 1992, Food and Drug Administration (FDA) issued a request for comments on labeling of biotechnology-based food products that are and a National Academy of Sciences report addresses pesticides in the diets of infants and children.

At the NABC 5 roundtable different scientific and personal views were expressed about the risks and benefits associated with various technologies. Specific products of biotechnology were selected to draw out a number of issues—the role of facts, values and emotions in assessing risk. Both, technical and other risks and benefits must be considered, though neither is easy to quantify.

According to Roger A. Balk, key elements of a risk assessment system to evaluate biotechnology products should be the principle of informed consent; scientific and statistical cost/benefit analysis; and a process to combine principles with data to guide regulation. Communication and the choice of which means of communication people turn to play a vital role in the public’s view on the risk of biotechnology. However, rarely does the public get insight into the extensive amount of data gathered during the regulatory process. While there is general optimism regarding agricultural biotechnology as a whole, there is more concern about specific products and desire from the public for more detailed information. Since newspapers tend to focus on controversial items they often select what the public wants, not necessarily what would be most important to provide information on which sound risk assessment can be based. There is a need to develop a better way to provide scientific education and information.

Hazard; risk; risk analysis; risk assessment; risk management, characterization and communication must be part of the regulatory process. Science (risk assessment) and policy/decision-making must be kept separate. While pharmaceuticals have long been regulated, agricultural products have not and it is not easy to fit agricultural research into the regulatory environment.

Four workshops were held and provided recommendations: 1. Technical Risk Assessment and Regulations; 2. Public Assessments of Benefits and Risks; 3. Public Values: Benefits and Harms; and 4. Public Communication about Risk

Recent Submissions

  • Roundtable 

    Martin, Marshal A. (NABC, 1993)
    Roundtable discussion by meeting participants and speaker panel
  • Public Values and Risk Assessment 

    Balk, Roger A. (NABC, 1993)
    There is great difficulty in exercising informed consent [in agricultural biotechnology] because the monolithic distribution system tends to restrict action to all or nothing.
  • Communicating with the public about risk 

    Bishop, Jerry E. (NABC, 1993)
    Inevitably, one interest group will accuse the media of needlessly scaring the public while another interest group will charge that the media are failing to alert the public to a deadly danger.
  • Telling public stories about risk 

    Dunwoody, Sharon (NABC, 1993)
    Learning how people use information to inform their risk judgments is difficult. One element is the influence of channel. Individuals will use different channels to help them make decisions about different dimensions of a ...
  • Risk assessment: A technical perspective 

    Fuchs, Roy L. (NABC, 1993)
    All three regulatory agencies in the U.S. issued draft or final policies during 1992 outlining their policies on regulating genetically engineered plants. The philosophy is based on the concept of “substantial equivalence.”

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