Download or read book Guidelines for the Clinical Evaluation of Drugs to Prevent Control and written by United States. Food and Drug Administration and published by . This book was released on 1978 with total page 4 pages. Available in PDF, EPUB and Kindle. Book excerpt:
Download or read book Guidelines for the Clinical Evaluation of Drugs to Prevent Control And or Treat Periodontal Disease written by United States. Food and Drug Administration and published by . This book was released on 1978 with total page 12 pages. Available in PDF, EPUB and Kindle. Book excerpt:
Download or read book Guidelines for the Clinical Evaluation of Drugs to Prevent Control And or Treat Periodontal Disease written by United States. Food and Drug Administration and published by . This book was released on 1978 with total page 4 pages. Available in PDF, EPUB and Kindle. Book excerpt:
Download or read book Guidelines for the Clinical Evaluation of Anti infective Drugs systemic written by United States. Food and Drug Administration and published by . This book was released on 1977 with total page 20 pages. Available in PDF, EPUB and Kindle. Book excerpt:
Download or read book Guidelines for the Clinical Evaluation of Anti infective Drugs systemic written by United States. Food and Drug Administration. Bureau of Drugs and published by . This book was released on 1977 with total page 20 pages. Available in PDF, EPUB and Kindle. Book excerpt:
Download or read book General Considerations for the Clinical Evaluation of Drugs written by United States. Food and Drug Administration and published by . This book was released on 1977 with total page 20 pages. Available in PDF, EPUB and Kindle. Book excerpt:
Download or read book General Considerations for the Clinical Evaluation of Drugs written by United States. Food and Drug Administration. Bureau of Drugs and published by . This book was released on 1977 with total page 20 pages. Available in PDF, EPUB and Kindle. Book excerpt:
Download or read book Guidelines for the Clinical Evaluation of Hypnotic Drugs written by United States. Food and Drug Administration and published by . This book was released on 1977 with total page 24 pages. Available in PDF, EPUB and Kindle. Book excerpt:
Download or read book General Considerations for the Clinical Evaluation of Drugs in Infants and Children written by United States. Food and Drug Administration. Bureau of Drugs and published by . This book was released on 1977 with total page 28 pages. Available in PDF, EPUB and Kindle. Book excerpt:
Download or read book General Considerations for the Clinical Evaluation of Drugs written by United States. Food and Drug Administration. Bureau of Drugs and published by . This book was released on 1977 with total page 20 pages. Available in PDF, EPUB and Kindle. Book excerpt:
Download or read book General Considerations for the Clinical Evaluation of Drugs in Infants and Children written by United States. Food and Drug Administration and published by . This book was released on 1977 with total page 28 pages. Available in PDF, EPUB and Kindle. Book excerpt:
Download or read book Improving Healthcare Quality in Europe Characteristics Effectiveness and Implementation of Different Strategies written by OECD and published by OECD Publishing. This book was released on 2019-10-17 with total page 447 pages. Available in PDF, EPUB and Kindle. Book excerpt: This volume, developed by the Observatory together with OECD, provides an overall conceptual framework for understanding and applying strategies aimed at improving quality of care. Crucially, it summarizes available evidence on different quality strategies and provides recommendations for their implementation. This book is intended to help policy-makers to understand concepts of quality and to support them to evaluate single strategies and combinations of strategies.
Download or read book Women and Health Research written by Institute of Medicine and published by National Academies Press. This book was released on 1994-02-01 with total page 286 pages. Available in PDF, EPUB and Kindle. Book excerpt: In the nineteenth century some scientists argued that women should not be educated because thinking would use energy needed by the uterus for reproduction. The proof? Educated women had a lower birth rate. Today's researchers can only shake their heads at such reasoning. Yet professional journals and the popular press are increasingly criticizing medical research for ignoring women's health issues. Women and Health Research examines the facts behind the public's perceptions about women participating as subjects in medical research. With the goal of increasing researchers' awareness of this important topic, the book explores issues related to maintaining justice (in its ethical sense) in clinical studies. Leading experts present general principles for the ethical conduct of research on womenâ€"principles that are especially important in the light of recent changes in federal policy on the inclusion of women in clinical research. Women and Health Research documents the historical shift from a paternalistic approach by researchers toward women and a disproportionate reliance on certain groups for research to one that emphasizes proper access for women as subjects in clinical studies in order to ensure that women receive the benefits of research. The book addresses present-day challenges to equity in four areas: Scientificâ€"Do practical aspects of scientific research work at cross-purposes to gender equity? Focusing on drug trials, the authors identify rationales for excluding people from research based on demographics. Social and Ethicalâ€"The authors offer compelling discussions on subjectivity in science, the evidence for male bias, and issues related to race and ethnicity, as well as the recruitment, retention, and protection of research participants. Legalâ€"Women and Health Research reviews federal research policies that affect the inclusion of women and evaluates the basis for researchers' fears about liability, citing court cases. Riskâ€"The authors focus on risks to reproduction and offspring in clinical drug trials, exploring how risks can be identified for study participants, who should make the assessment of risk and benefit for participation in a clinical study, and how legal implications could be addressed. This landmark study will be of immediate use to the research community, policymakers, women's health advocates, attorneys, and individuals.
Download or read book Guidelines for the Clinical Evaluation of Drugs to Prevent Dental Caries written by United States. Food and Drug Administration and published by . This book was released on 1978 with total page 16 pages. Available in PDF, EPUB and Kindle. Book excerpt:
Download or read book Principles for the Clinical Evaluation of Drugs written by World Health Organization. Scientific Group on Principles for the Clinical Evaluation of Drugs and published by . This book was released on 1968 with total page 32 pages. Available in PDF, EPUB and Kindle. Book excerpt: Guidelines established by the World Health Organization Scientific Group on Principles for the Clinical Evaluation of Drugs (Geneva, 1967) are summarized. Clinical introduction of druggs developed from work with laboratory animals should be preceded by carefully planned human investigations within several scientific disciplines including biochemistry, pharmacology and toxicology, clinical pharmacology, clinical medicine, and medical statistics. Formal therapeutic trial should begin only after an initial therapeutic potential has been established through close study of a few individuals. Improved human evaluation of drugs requires better laboratory facilities and more highly trained personnel and might be achieved by the creation of more clinical pharmacology units within medical centers. Future emphasis should be placed on developing better techniques for measuring absorption, distribution, and excretion of drugs and their metabolites, and for accurate detection of toxic effects. The ethical and technical complexities of drug evaluation require thorough planning discussions with a local medical and scientific committee, rather than an official control organization, before initial investigation is begun. Methods should be established for compensating subjects suffering ill health or injury during the course of experimentation, even where there is no question of legal liability for negligence. Prompt dissemination of all relevant information concerning new drugs should be included as an integral part of every investigation. Monitoring of adverse reactions to drugs in widespread use requires extensive, additional research which should focus on the elaboration of methods that will provide early warning of drug-related toxicity as well as incidence figures that can be used to quantify associated risks.
Download or read book Guidelines for the Clinical Evaluation of Radiopharmaceutical Drugs written by United States. Food and Drug Administration. Bureau of Drugs and published by . This book was released on 1981 with total page 24 pages. Available in PDF, EPUB and Kindle. Book excerpt:
Download or read book Guidelines for the Clinical Evaluation of Radiopharmaceutical Drugs written by United States. Food and Drug Administration. Division of Oncology and Radiopharmaceutical Drug Products and published by . This book was released on 1981 with total page 24 pages. Available in PDF, EPUB and Kindle. Book excerpt:
