Challenges for the FDA : the Future of Drug Safety : Workshop Summary /

Detalles Bibliográficos
Clasificación:Libro Electrónico
Autores Corporativos: Symposium on the Future of Drug Safety: Challenges for the FDA Washington, D.C., Institute of Medicine (U.S.). Forum on Drug Discovery, Development, and Translation
Otros Autores: Pray, Leslie A., Robinson, Sally
Formato: Electrónico Congresos, conferencias eBook
Idioma:Inglés
Publicado: Washington, DC : National Academies Press, ©2007.
Colección:Online access: NCBI NCBI Bookshelf.
Temas:
United States. > Food and Drug Administration > Rules and practice.
United States > Food and Drug Administration > rules & practice
United States > Food and Drug Administration
United States. > Food and Drug Administration
Drugs > United States > Testing > Congresses.
Drugs > United States > Safety measures > Congresses.
Drugs > Side effects.
Pharmacovigilance.
Drugs > Side effects > Reporting.
Drug monitoring.
Drug interactions.
Drug-Related Side Effects and Adverse Reactions > prevention & control
United States Food and Drug Administration
Drug Approval > organization & administration
Drug-Related Side Effects and Adverse Reactions
Drug Approval
Safety
Pharmacovigilance
Drug Monitoring
Drug Combinations
Product Surveillance, Postmarketing
Product Surveillance, Postmarketing > standards
Adverse Drug Reaction Reporting Systems > organization & administration
Drug Evaluation, Preclinical > standards
Drug Interactions
Government Agencies
Médicaments > États-Unis > Essais cliniques > Congrès.
Médicaments > États-Unis > Sécurité > Mesures > Congrès.
Médicaments > Effets secondaires.
Interactions médicamenteuses.
MEDICAL > Drug Guides.
MEDICAL > Pharmacology.
MEDICAL > Pharmacy.
MEDICAL > Nursing > Pharmacology.
Drugs > Side effects > Reporting
Drugs > Side effects
Drug monitoring
Drug interactions
Drugs > Safety measures
Drugs > Testing
United States
Congress
Rules and practice
proceedings (reports)
Conference papers and proceedings
Rules
Conference papers and proceedings.
Actes de congrès.
Acceso en línea:Texto completo
Tabla de Contenidos:
  • Addressing the FDA's Resource Challenges
  • Strengthening the Scientific Base of the Agency
  • Integrating Pre- and Postmarket Review
  • Enhancing Postmarket Safety Monitoring
  • Conducting Confirmatory Drug Safety and Efficacy Studies
  • Enhancing the Value of Clinical Trial Registration
  • Enhancing Postmarket Regulation and Enforcement
  • Looking to the Future.

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