Writing clinical research protocols : ethical considerations

Writing clinical research protocols ethical considerations

Detalles Bibliográficos
Autor principal: DeRenzo, Evan G. (-)
Otros Autores: Moss, Joel
Formato: Libro
Idioma:Inglés
Publicado: Amsterdam [etc.] : Elsevier-Academic cop. 2006.
Materias:
Ensayos clínicos > Aspectos morales.
Experimentación humana en medicina > Aspectos morales.
Medicina > Casos, historias clínicas, estadísticas.
Escritos médicos.
Ver en Universidad de Navarra:https://unika.unav.edu/discovery/fulldisplay?docid=alma991002698959708016&context=L&vid=34UNAV_INST:VU1&search_scope=34UNAV_TODO&tab=34UNAV_TODO&lang=es
Tabla de Contenidos:
  • Introduction to the art and science of clinical research
  • What you need to know about clinical research ethics
  • What you need to know about the regulation of clinical research
  • Designing a clinical research study
  • Selecting subjects for clinical studies
  • Risks and benefits in clinical research
  • Recruiting subjects
  • Informed consent
  • Privacy and confidentiality
  • The "ethics" section
  • Procedures and methods
  • Statistics, data collection and management, and record keeping
  • Use of human biological materials
  • Special issues raised by evolving areas of clinical research
  • Case histories : learning from experience.

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