Veterinary Pharmacovigilance is an in-depth examination of veterinary pharmacovigilance, looking at the scientific methodologies involved, the role of regulatory agencies and legislation, and the underpinning science.

Veterinary pharmacovigilance is a rapidly growing discipline in both regulatory and scientific terms, and its importance can only increase as regulatory agencies across the globe seek to improve their hazard and risk assessment of marketed veterinary medicines by applying the techniques of post-marketing surveillance.

Veterinary Pharmacovigilance will be fundamentally important reading for all involved in the field of veterinary pharmacovigilance including veterinarians, physicians, environmental scientists, regulators and those involved in drug development and market maintenance.

Contents

1. Elements of Veterinary Pharmacovigilance
2. Veterinary Pharmacovigilance in the European Union
3. Pharmacovigilance and the European Medicines Agency: Conduct of Pharmacovigilance Activities
4. Veterinary Pharmacovigilance in France
5. Pharmacovigilance in Germany
6. Veterinary Pharmacovigilance: the UK Experience
7. Veterinary Adverse Drug Reporting in the United States, Australia and Canada
8. Veterinary Pharmacovigilance: A South African Perspective
9. Pharmacovigilance Inspections in the European Union
10. Essential Elements of Veterinary Pharmacovigilance and the Role and Duties of the Qualified Person
11. Veterinary Pharmacovigilance in an Industry Setting: The EU
12. Pharmacovigilance in the US: Industry Perspective
13. Practical Veterinary Pharmacovigilance
14. Preclinical Safety Testing and Assessment of Veterinary Pharmaceuticals and Pharmacovigilance
15. Safety Assessment of Veterinary Vaccines
16. Microbiological Assessment of Veterinary Medicinal Products and Potential Adverse Effects
17. Adverse Effects of Veterinary Pharmaceutical Products in Animals
18. Adverse Drug Reactions in Dogs: Toxic Hepatic Responses
19. Adverse Reactions to Vaccines
20. Adverse Reactions in Humans Following Exposure to Veterinary Drugs
21. Medicines Used to Control and Treat External Parasites of Sheep: Toxicology and The Phenomenon of Reported Adverse Human Responses to Organophosphorus Sheep Dips
22. User Safety Assessment of Veterinary Medicinal Products
23. Maximum Residue Limits
24. Determination of Withdrawal Periods for Pharmaceutical Products Used in Food Animals
25. Surveillance for Veterinary Residues
26. Adverse Environmental Effects and Veterinary Medicinal Products
27. Causality in Pharmacovigilance and Expectedness of Adverse Reactions
28. Quantitative Aspects of Veterinary Pharmacovigilance
29. Veterinary Adverse Reactions and Crisis Management
30. The Role of Veterinary Pharmacovigilance in Risk Analysis and the Influence of Risk Perception on Veterinary Pharmacovigilance
31. The Role of Quality Assurance in Veterinary Pharmacovigilance
32. Concordance Between Results from Animal Toxicology Studies and Adverse Reactions in Animals

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