Safety Evaluation of Pharmaceuticals and Medical Devices International Regulatory Guidelines /

Safety Evaluation of Pharmaceuticals and Medical Devices has been written to provide complete, ready and clear guidance as to what nonclinical safety assessment tests need to be performed to move a regulated therapeutic medical product into and through the development process and to marketing approv...

Πλήρης περιγραφή

Λεπτομέρειες βιβλιογραφικής εγγραφής
Κύριος συγγραφέας: Gad, Shayne C. (Συγγραφέας)
Συγγραφή απο Οργανισμό/Αρχή: SpringerLink (Online service)
Μορφή: Ηλεκτρονική πηγή Ηλ. βιβλίο
Γλώσσα:English
Έκδοση: Boston, MA : Springer US, 2011.
Θέματα:
Διαθέσιμο Online:Full Text via HEAL-Link
Πίνακας περιεχομένων:
  • Preface
  • Introduction to Safety Assessment in Drug and Medical Device Development
  • Drugs: The General Case
  • Ind Enabling Toxicology Programs
  • Nonclinical Safety Evaluation Studies Conducted To Support Continued Clinical Development
  • Supporting Marketing Applications
  • Special Therapeutic Category And Route Of Administration Cases
  • Device Safety Evaluation
  • Appendix A
  • INDEX.