Principles and practice of pharmaceutical medicine /
| Corporate Author: | |
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| Other Authors: | , , |
| Format: | eBook |
| Language: | English |
| Published: |
Oxford, UK :
Wiley-Blackwell,
2011.
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| Edition: | Third edition. |
| Subjects: | |
| Online Access: | Connect to the full text of this electronic book. |
Table of Contents:
- The Practice and Practitioners of Pharmaceutical Medicine
- Pharmaceutical Medicine as a Medical Specialty
- Clinical Research Education and Training for Biopharmaceutical Staff
- Drug Discovery: Design and Development
- Translational Medicine, Pharmaceutical Physicians, Patients, and Payers
- Pharmaceutics
- Nonclinical Toxicology
- Informed Consent
- Phase I: The First Opportunity for Extrapolation from Animal Data to Human Exposure
- Phase II and Phase III Clinical Studies
- Phase IV Drug Development: Post-Marketing Studies
- Site Management
- Good Clinical Practices
- Quality Assurance, Quality Control and Audit
- The Unique Role of Over-the-Counter Medicine
- Drug Research in Older Patients
- Drug Development Research in Women
- Clinical Research in Children
- Racial and Ethnic Issues in Drug Regulation
- Special Populations: Hepatic and Renal Failure
- Drug Interactions
- Orphan Drugs
- QT Interval Prolongation and Drug Development
- Biotechnology Products and Their Development
- Health Economics
- Pharmacoeconomics: Economic and Humanistic Outcomes
- Pharmacoepidemiology and the Pharmaceutical Physician
- Statistical Principles and Application in Biopharmaceutical Research
- Data Management
- Patient Compliance: Pharmionics, A New Discipline
- Monitoring Drug Concentrations in Clinical Practice
- Generics
- Complementary Medicines
- United States Regulations
- Special US Regulatory Procedures: Emergency and Compassionateâ‚„ INDs and Accelerated Product Approvals
- The Development of Human Medicines Control in Europe from Classical Times to the 21st Century
- Medicines Regulation in the European Union
- Japanese Regulations
- Drug Registration and Pricing in the Middle East
- China's Regulated Pharmaceutical Market
- India's New Era in Pharmaceuticals
- Medical Affairs
- Drug Labeling
- Data Mining
- Risk Management in Product Approval and Marketing
- Publishing Clinical Studies
- Organizing and Planning Local, Regional, National, and International Meetings and Conferences
- When Things Go Wrong: Drug Withdrawals from the Market
- International Trials: Successful Planning and Conduct
- Introduction to Bioethics for Pharmaceutical Professionals
- Pharmaceutical Medicine and the Law
- Fraud and Misconduct in Clinical Research
- The Multinational Corporations: Cultural Challenges, the Legal/Regulatory Framework and the Medico-Commercial Environment
- Advertising and Marketing
- Pharmaceutical Product Liability
- Patents
- Outsourcing Clinical Drug Development Activities to Contract Research Organizations (CROs): Critical Success Factors
- The Impact of Managed Care on the US Pharmaceutical Industry
- Appendix: Useful Web Links.