2 edition of Legal considerations: drug abuse in industry and business found in the catalog.
Legal considerations: drug abuse in industry and business
Sidney H. Willig
|Statement||[by] Sidney H. Willig. Edited by W. Wayne Stewart.|
|LC Classifications||KF3829.N2 W5|
|The Physical Object|
|Pagination||xiv, 101 p.|
|Number of Pages||101|
|LC Control Number||77151994|
As explained by Tribe"until the early s, the Supreme Court routinely upheld sexually discriminatory laws whenever they could be rationally related to government purposes reflecting traditional views of the 'proper' relationship between men and women in American society. Read more Book Topics. Curr Pharm Des ; 20 13 : The Supreme Court has concluded that the equal protection clause restricts the right of the government to treat similarly situated persons and groups differently.
For example, many states, through their courts and state legislatures, have adopted portions of the Restatement Second of Torts, the American Law Institute's synthesis of the major principles of contemporary tort law ALI, Cannabis use in first episode psychosis: Meta-analysis of prevalence, and the time course of initiation and continued use. United States. Finally, while it is necessary that there be some injury in order to recover damages, the injury need not necessarily be tangible.
Pharmacol Ther ; Etzel, and Doug Hankes If the counselor chooses to use client data for teaching purposes, she must do so in a manner that conceals the identity of the client. Watson II and Edward F. The substance abuse counselor is obligated to maintain the confidentiality of all client sessions.
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Your agency must refer all employees found to use illegal drugs to the EAP for assessment, counseling, and referral for appropriate 'treatment or rehabilitation. Finding no intent to discriminate, the Court then cited the state's "legitimate interest in maintaining a self-supporting The most common application of negligence in the area of research injury is lack of informed consent.
References:  National Conference of State Legislatures. NIH and FDA do not require investigators or sponsors to report research injuries, and there is no registry of injuries for publicly or privately sponsored research. Creating a compliance program for a small generic drug manufacturer.
Finally, the Act mandates the creation of a national data system and clearinghouse on research for women's health see Chapter 2. IOM, ; Wittes and Wittes, Johnson Controls was brought under a federal civil rights statute governing private sector discrimination in the terms and conditions of employment, but the notion that it is wrongfully discriminatory to exclude women from a benefit on grounds of fetal protection could apply by analogy to the context of clinical studies.
In limited circumstances, however, certain employers may be able to demonstrate that it is job-related and consistent with business necessity to require employees in positions affecting public safety to report when they are taking medication that may affect their ability to perform essential functions.
They further recommended that a "woman of childbearing potential" be excluded from "large-scale clinical trials" i. JAMA Psychiatry ; 74 6 : Precautions in clinical trials including women of childbearing potential FDA will rely on the informed consent document and the investigator's brochure to advise participants of the need to take precautions to prevent the inadvertent exposure of a fetus to potentially toxic drugs.
Drug Alcohol Depend ; : The following sections discuss the incidence of research injuries, the legal theories that could serve as the basis for legal action, and the individuals and entities that might be found liable. United States.
This argument may be particularly strong when made on behalf of women suffering from terminal illnesses who seek access to experimental drug therapies. Some states have attempted to control the behavior of pregnant women in order to protect fetuses.
Furthermore, NIH is instructed to conduct or support outreach programs for recruitment and retention of women and racial and ethnic group participants in clinical research projects. Headache ; 55 6 : Voluntary participation of respondents in the research is important.
But in one case where an injured plaintiff claimed FDA made a decision to release a polio vaccine based on inadequate animal test data, the court held that FDA's assessment of the animal data was a scientific determination, not the exercise of a discretionary function, and thus subject to liability Griffin v.
Respondents should participate on the basis of informed consent. They are provided as an aid to organizations involved in the evaluation of new drugs for FDA approval who wish to market such drugs.
The federal government cannot be sued for injuries resulting from the negligence of persons not directly employed by the federal government but who are working with full or partial federal financial support. Etzel and Jack C. The pharmacologic and clinical effects of medical cannabis.
For example, if evidence is found that the benefits of participating in research accrue disproportionately to men, it could be argued that the federal research policies effectively result in disparate treatment of men and women.
IRBs and research institutions The research institution and its IRB may also be held liable for approving a negligent protocol or for not closely monitoring or supervising the ongoing research.23 latest healthcare industry lawsuits, settlements while generic drug companies say the changes will help control drug prices.
To receive the latest hospital and health system business. Ethical Issues Related to Drug Abuse & Addiction. The National Institute on Drug Abuse reports that there were over 64, deaths from drug overdose in In states where marijuana is. Cocaine and heroin abuse claim the lives of more than 15, Americans every year, but no pathologist sits on the advisory board that passes on drug research grants, and there is no federal funding for pathology or for pathologists interested in drug abuse.
The sorry state of. Ethical Issues in Sport, Exercise, and Performance Psychology focuses on a multitude of unique ethical, legal, and related professional challenges faced by sport, exercise, and performance psychology practitioners.
The book contains seventeen chapters organized into four sections: I. Ethical Practices. Jul 11, · As of now the DEA schedules drugs based on three criteria: their potential for abuse and addiction, whether or not they have any accepted medical use, and whether or not there are standardized safety protocols for using the drug.
Thus, in the eyes of the federal government, marijuana is a ‘highly addictive drug with zero medical benefits’. Human Resources Learn more about the laws you must follow in the workplace -- and strategies and tips for staying out of legal trouble when dealing with employees.
Whether you need to know more about the Family and Medical Leave Act, progressive discipline, overtime, workplace safety, employee privacy, employee handbooks, or wrongful.