Stinging the Detroit criminal: A total system perspective

The success of sting operations (fake-fences) has been reported widely with impressive aggregate statistics on arrests and convictions. In this paper, we present a more detailed view of a successful Detroit sting program. We follow a sting participant's involvement from the time he entered the storefront until final sentencing, the result of the sting. Previously unreported statistics that we present include prior convictions and sentences for those involved in the sting, the number of sales an individual made to the sting and data on final sentences. More importantly we explore relationships between the various statistics. Our most important finding is that a sting operation is an effective way of getting criminals off the streets for extended periods of time. Eighty percent of those convicted for receiving and concealing stolen property were incarcerated, and the average minimum sentence was 19 months. The data also suggest the importance of multiple sales by an individual to the sting. The number of sales was shown to affect both the likelihood of conviction and the type of sentence imposed.     

Protecting health information privacy in research: what's an ethics committee like yours doing in a job like this?

The Commonwealth and State legislation designed to protect the privacy of personal health information has attracted the criticism that the constraints imposed on the use of the information in research obstructs that research. A central and common feature of the legislation is the reliance upon the review by human research ethics committees of research that proposes to use personal health information for research without prior consent from those whose information it is. The origins of this reliance are explored and explained and it is suggested that this has proved to be an inappropriate policy choice. The extension of the reliance is then described and the conceptual, procedural, workload and structural consequences of requiring these voluntary committees to conform to legislative standards of review of issues of the public interest are critically examined. In recent reviews of the Commonwealth legislation, there is recognition of the underlying uncertainty as to the appropriate balance between protection of personal privacy and the promotion of beneficial research. In the further exploration of these matters that those reviews recommended, a close and critical examination of the wisdom of continuing to rely on ethics committees is needed.     

The Emergence of Environmental Concerns: Hydroelectric Schemes in Scotland

Regulating the environmental impacts of hydroelectric schemesis of increasing importance in the light of the strong policydrive towards expanding the proportion of energy gained fromrenewable sources. Yet hydroelectric schemes are significantin another way. They provide an unusual example of a technologythat has changed little over the last 100 years and thus offersa real opportunity to judge the impact of a changing regulatoryclimate. In Scotland, three distinct phases can be detected.Earlier controls focussed on the protection of private interests,especially fishing rights, with authorisations secured throughPrivate Acts of Parliament. This was followed by a period wherepromotion of such schemes lay with public bodies; though undergeneral statutory duties, ultimately the balancing of environmentaland other interests lay with such bodies who acted with fewexternal controls. Privatisation of electricity generation in1989, coupled with the growing development of relevant EuropeanCommunity legislation, dramatically shifted the regulatory balances.Environmental Assessment requirements and now the obligationsof the Water Framework Directive have substantially alteredthe concept and scope of environmental concerns in this field.     

Patient information on drug therapy. A problem of medical malpractice law: between product safety and user safety

Medicinal products are associated with risks as well as potential therapeutic benefits. This is reflected by the legal requirements for patient information on drug therapy which can be differentiated into general product information, regulated by pharmaceutical (i. e. product safety) law, and individual patient information on the treatment with the product, which is subject to medical malpractice law. The physician's duty to inform the patient comprises therapeutic information as well as information required for informed consent. Therapeutic information intends to empower the patient to comply with the requirements of treatment and to protect him/her against preventable danger and risk; it is part of the medical treatment, aimed at the individual patient and his/her personal situation. Information required for informed consent enables the patient to a self-determined decision on the treatment offered; it can be divided into information on the course of treatment and risk information. Product information and treatment information complement each other; the former should be the basis of individual information on the concrete treatment, provided by the physician in a mandatory oral conversation with the patient. Product information cannot replace the physician's individual information about the treatment.     

“零容忍”反腐败:内涵、特征与进路

本文在研究"零容忍"反腐败的内涵和特征以及借鉴新加坡和香港"零容忍"反腐败的基础上,提出"零容忍"反腐败的进路思考。"零容忍"反腐败要建立一套完整有效的法律制度,形成一支坚强有力的执行队伍,加强执行权威,建构一个公民参与的、广泛细化的反腐败网络,也要通过反腐败教育提高公民反腐败意识和公务员廉洁奉公的情操。