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R. Cory Watkins Lorraine Green Mazerolle Dennis Rogan 《American Journal of Criminal Justice》2000,24(2):217-233
This paper examines the environmental and social structural correlates associated with random gunfire incidents. The study
group consists of 273 face blocks and intersections in a selected portion of Dallas, Texas. The data show some locations routinely
generate random gunfire, while others remain gunshot-free. The analysis suggests environmental factors are not sufficient
to explain random gunfire. Implications for future inquiries are offered.
The research for this paper was supported by Grant No. DOJ-OH-6-8971 from the National Institute of Justice. Findings and
conclusions of the research reported here are those of the authors and do not necessarily reflect the official position or
policies of the U.S. Department of Justice. The authors are indebted to the support from the Dallas Police Department with
special appreciation to Sgt. Mark Stallo, Sgt. Bruce McDonald, and Southwest Crime Analyst Mike Edgar. Thanks also go to James
Frank from the University of Cincinnati and Kasaundra Tomlin from the University of Central Florida. 相似文献
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Alan Bennett Freddy Jiménez Larry Eugene Fields Joshua Oyster 《Journal of Law and the Biosciences》2015,2(2):168-212
The US Food and Drug Administration''s (‘FDA’ or the ‘Agency’) current regulatory framework for drug promotion, by significantly restricting the ability of drug manufacturers to communicate important, accurate, up-to-date scientific information about their products that is truthful and non-misleading, runs afoul of the First Amendment and actually runs counter to the Agency''s public health mission. Our article proposes a New Model that represents an initial proposal for a modern, sustainable regulatory framework that comprehensively addresses drug promotion while protecting the public health, protecting manufacturers’ First Amendment rights, establishing clear and understandable rules, and maintaining the integrity of the FDA approval process. The New Model would create three categories of manufacturer communications—(1) Scientific Exchange and Other Exempt Communications, (2) Non-Core Communications, and (3) Core Communications—that would be regulated consistent with the First Amendment and according to the strength of the government''s interest in regulating the specific communications included within each category. The New Model should address the FDA''s concerns related to off-label speech while protecting drug manufacturers’ freedom to engage in truthful and non-misleading communications about their products. 相似文献
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