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21Publicado 2011Materias: “…United States. Food and Drug Administration Periodicals…”
Tesis -
22Publicado 2008Materias: “…United States. Food and Drug Administration…”
Universidad Loyola - Universidad Loyola Granada (Otras Fuentes: Biblioteca de la Universidad Pontificia de Salamanca)Enlace del recurso
Libro electrónico -
23por Symposium on the Future of Drug Safety: Challenges for the FDAMaterias: “…United States. Food and Drug Administration Rules and practice…”
Publicado 2007
Libro electrónico -
24Publicado 2011Tabla de Contenidos: “…""Front Matter""; ""Reviewers""; ""Contents""; ""Abbreviations""; ""1 Introduction""; ""2 Food and Drug Administration Postmarket Surveillance Activities and Recall Studies of Medical Devices""; ""3 Non-Food and Drug Administration Sources of Adverse Event Data""; ""4 Postmarket Surveillance of Medical Devices: Panel Discussion""; ""5 Other Select Topics""; ""Appendix A: Workshop Agenda""; ""Appendix B: Biographic Information on Invited Speakers, Panelists, and Authors of Commissioned Papers""; ""Appendix C: 510(k) Premarket Notification Analysis of FDA Recall Data""…”
Libro electrónico -
25Publicado 1982Materias: “…United States. Food and Drug Administration Periodicals…”
Tesis -
26por Weinberg, Sandy, 1950-Materias: “…United States. Food and Drug Administration…”
Publicado 2011
Universidad Loyola - Universidad Loyola Granada (Otras Fuentes: Biblioteca de la Universidad Pontificia de Salamanca)Enlace del recurso
Libro electrónico -
27
Acceso restringido, con credenciales UPSA
Recurso de actualización contínua -
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29Publicado 2022Materias:Libro electrónico
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30Publicado 2022Materias: “…United States Food and Drug Administration-approved drug…”
Libro electrónico -
31Publicado 2022Materias:Libro electrónico
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34Publicado 2012Tabla de Contenidos: “…Thomas Ten Have""; ""Contents""; ""Abstract""; ""Summary""; ""1 Introduction""; ""2 Incorporating Benefit and Risk Assessment and Benefit-Risk Management into Food and Drug Administration Decision-Making""; ""3 Evidence and Decision-Making""; ""4 Selection and Oversight of Required Postmarketing Studies""; ""5 Synthesis""; ""Appendix A: Other Elements of the Food and Drug Administration Amendments Act""; ""Appendix B: Committee's Letter Report""; ""Appendix C: Open Session Agendas""…”
Libro electrónico -
35Publicado 2009Tabla de Contenidos: “…Introduction and overview -- Current model for financing drug development : from concept through approval -- The Food and Drug Administration's Orphan Drug Program -- Diverse funding models -- Strategies for facilitating sharing of research materials and data -- Strategies of navigation intellectual property -- Strategies for facilitating clinical trials -- Summary…”
Libro electrónico -
36por National Academies of Sciences, Engineering, and Medicine (U.S.).Tabla de Contenidos: “…Introduction and context -- Emerging trends and products of biotechnology -- The current biotechnology regulatory system -- Understanding risks related to future biotechnology products -- Opportunities to enhance the capabilities of the biotechnology regulatory system -- Conclusions and recommendations -- Glossary -- Appendix A: Biographical sketches of committee members -- Appendix B: Agendas of information-gathering sessions -- Appendix C: Requests for information -- Appendix D: Congressionally defined product categories that the U.S. Food and Drug Administration regulates…”
Publicado 2017
Libro electrónico -
37por Andre, Linda, 1959-Tabla de Contenidos: “…The trouble with time -- Eugenic conceptions I : ticking time bombs -- Eugenic conceptions II : useless eaters -- A little brain pathology -- Informed consent and the dawn of the public relations era -- The American Psychiatric Association Task Force -- The making of an American activist -- The ECT industry cows the media -- Long strange trip : ECT and the food and drug administration -- The Committee for Truth in Psychiatry -- Anecdote or evidence? …”
Publicado 2009
Libro electrónico -
38
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39Publicado 2022“…It presents the latest findings on the toxic effects of BPA, diseases that may be related to bisphenol exposure, and the regulations of the US Food and Drug Administration, European Food Safety Authority, and European Union…”
Libro electrónico -
40Publicado 1991Tabla de Contenidos: “…Biomedical Politics -- Copyright -- Preface -- Acknowledgments -- Contents -- Introduction -- References -- Unproven AIDS Therapies: The Food and Drug Administration and DDI -- THE DRUG REGULATION PROCESS -- The Drug Approval Process Today -- Speeding Up the Process: The "Bush Initiative -- Prelicensing Availability -- PARALLEL TRACK -- PARALLEL TRACK: PROS AND CONS -- The Food and Drug Administration -- The Research Community -- The AIDS Activists -- Other Consumer Interests -- EARLY RELEASE OF DDI -- MOTIVATIONS -- Bristol-Myers -- The Food and Drug Administration -- The National Institutes of Health -- The Activists -- CONCLUSIONS -- NOTES -- REFERENCES -- Commentary -- LEON EISENBERG -- Commentary -- PETER F. …”
Libro electrónico