Pharmacovigilance: A Practical Approach
Elsevier - Health Sciences Division (Verlag)
978-0-323-58116-5 (ISBN)
Covers the evolving regulatory landscape, as well as current and future use of digital technologies.
Uses case studies to ensure content is relevant to everyday practice.
Discusses behavioral science and patient perspectives, risk communication, and new frontiers in pharmacovigilance.
Consolidates today's available information on this timely topic into one convenient resource.
Introduction
1. Does Regulation Drive Science or Does Science Drive Regulation?
2. Role of Epidemiology in Pharmaceutical Industry
3. Real World Epidemiologic Studies and Patient Registries
Section III. Benefit-Risk in the Drug Development Life Cycle
4. Signal Management and Methods of Signal Detection
5. Causality Assessment and Examples of Adverse Drug Reactions (Drug Induced Liver Injury, Skin, Major Adverse Cardiac Events and Renal)
6. Product Safety Monitoring in Clinical Trials
7. Benefit-Risk Assessments
8. Communicating benefit risk
9. Pharmacovigilance and Medical Devices
10. Vaccine Safety Surveillance
11. Pharmacovigilance in Special Populations (Pediatrics and Elderly)
12. Pharmacovigilance in Pregnancy
13. Impact and Implications of Technology on Pharmacovigilance
14. The Future of Pharmacovigilance
Erscheinungsdatum | 19.09.2018 |
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Verlagsort | Philadelphia |
Sprache | englisch |
Maße | 191 x 235 mm |
Gewicht | 480 g |
Themenwelt | Medizin / Pharmazie ► Medizinische Fachgebiete ► Pharmakologie / Pharmakotherapie |
Medizin / Pharmazie ► Pharmazie | |
ISBN-10 | 0-323-58116-1 / 0323581161 |
ISBN-13 | 978-0-323-58116-5 / 9780323581165 |
Zustand | Neuware |
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