Methodological considerations in the design of trials for safety assessment of new drugs and chemical entities

Lignende værker

• Equivalence and noninferiority trials – are they viable alternatives for registration of new drugs? (III)
  af: Pater, Cornel
  Udgivet: (2004)
• Drug safety assessment in clinical trials: methodological challenges and opportunities
  af: Singh, Sonal, et al.
  Udgivet: (2012)
• Safety assessment of adjuvanted vaccines: Methodological considerations
  af: Da Silva, Fernanda Tavares, et al.
  Udgivet: (2015)
• Methodological Considerations in the Design and Implementation of Clinical Trials
  af: Cirrincione, Constance T., et al.
  Udgivet: (2013)
• New technologies in computer-aided drug design: Toward target identification and new chemical entity discovery
  af: Tang, Yun, et al.
  Udgivet: (2006)