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...
Κύριος συγγραφέας: | |
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Συγγραφή απο Οργανισμό/Αρχή: | |
Μορφή: | Ηλεκτρονική πηγή Ηλ. βιβλίο |
Γλώσσα: | English |
Έκδοση: |
Boston, MA :
Springer US,
2011.
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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.