Pharmaceutical Medicine and Translational Clinical Research

Herausgeber: Vohora, Divya; Singh, Gursharan

• Broschiertes Buch

Produktbeschreibung

Pharmaceutical Medicine and Translational Clinical Research covers clinical testing of medicines and the translation of pharmaceutical drug research into new medicines, also focusing on the need to understand the safety profile of medicine and the benefit-risk balance. Pharmacoeconomics and the social impact of healthcare on patients and public health are also featured. It is written in a clear and straightforward manner to enable rapid review and assimilation of complex information and contains reader-friendly features.As a greater understanding of these aspects is critical for students in the areas of pharmaceutical medicine, clinical research, pharmacology and pharmacy, as well as professionals working in the pharmaceutical industry, this book is an ideal resource.

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Produktdetails

• Verlag: Elsevier Science Publishing Co Inc
• Seitenzahl: 526
• Erscheinungstermin: 13. November 2017
• Englisch
• Abmessung: 235mm x 195mm x 30mm
• Gewicht: 1046g
• ISBN-13: 9780128021033
• ISBN-10: 0128021039
• Artikelnr.: 48023994

Inhaltsangabe

Section I- Overview of Pharmaceutical Medicine 1. The Specialty of
Pharmaceutical Medicine
Section II- Drug Discovery and Development 2. Drug Discovery and
Development: An overview 3. Pharmaceutical Development 4. Preclinical Drug
Development 5. Target Product Profile and Clinical Development Plan 6.
Clinical Pharmacokinetics and Drug Interactions 7. Pharmacogenomics: An
Evolution Towards Clinical Practice 8. Clinical Research Quality Assurance
and Audits
Section III- Pharmaceutical Law and Ethics 9. Pharmaceutical Medicine and
Law 10. Pharmaceutical Regulations in the United States 11. Pharmaceutical
Regulations in European Union 12. Pharmaceutical Regulations in India 13.
Pharmaceutical Regulations for Complementary Medicine 14. Ethical
Considerations in Clinical Research
Section IV- Pharmaceutical Industry and Intellectual Property Rights 15.
Patent 16. Copyright 17. Trademark 18. Trade Secret 19. Data Exclusivity
Section V- Generics, Supergenerics, Biologics, biosimilars and bio-betters
20. Generic Drug and Bioequivalence Studies 21. Vaccines 22. Biosimilars
23. Re-innovation in Pharmaceutical Industry: Supergenerics and Biobetters
Section VI- Medical Services 24. Phase IV Studies and Lifecycle Management
25. Medical Affairs
Section VII- Pharmacovigilance 26. Pharmacovigilance and Drug Safety 27.
Clinical and Post Approval Safety Data Management 28. Individual Case
Safety Reports 29. Development and Periodic Safety Reports 30. Risk
Management in Pharmacovigilance 31. Recent Developments in
Pharmacovigilance at UMC
Section VIII- Drug utilization and Pharmacoeconomics 32. Assessing Medicine
Use and Tools for Monitoring Medicine Use 33. Pharmacoeconomics and
Healthcare