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| Link zu diesem Datensatz | https://d-nb.info/1380670632 |
| Titel | Introduction to Basics of Pharmacology and Toxicology : Volume 4: Pharmacology and Therapeutics / edited by Avinash Arivazhahan, Neel Shah, Selvarajan Sandhiya, Gerard Marshall Raj |
| Person(en) |
Arivazhahan, Avinash (Herausgeber) Shah, Neel (Herausgeber) Sandhiya, Selvarajan (Herausgeber) Raj, Gerard Marshall (Herausgeber) |
| Organisation(en) | SpringerLink (Online service) (Sonstige) |
| Ausgabe | 1st ed. 2025 |
| Verlag | Singapore : Springer Nature Singapore, Imprint: Springer |
| Zeitliche Einordnung | Erscheinungsdatum: 2025 |
| Umfang/Format | Online-Ressource, XXVII, 547 p. 62 illus., 52 illus. in color. : online resource. |
| Andere Ausgabe(n) |
Printed edition:: ISBN: 978-981-95-1919-4 Printed edition:: ISBN: 978-981-95-1921-7 Printed edition:: ISBN: 978-981-95-1922-4 |
| Inhalt | 1. Clinical Pharmacokinetics -- 2. Essential medicines and rational use of drugs -- 3. Drug Information Centre -- 4. Evidence-Based Medicine -- 5. Medication Adherence -- 6. Therapeutic Drug Monitoring -- 7. Medication Error -- 8. Drug use in pregnancy and lactation (Perinatal pharmacology) -- 9. Pediatric Pharmacology -- 10. Geriatric Pharmacology -- 11. Usage of drugs in various Pathological States -- 12. High throughput screening and computer-aided drug designing -- 13. Phase 0 Clinical Trials -- 14. Phase 1 Clinical Trials -- 15. Phase 2 Clinical Trials -- 16. Phase 3 Clinical Trials -- 17. Phase 4 Clinical trials -- 18. Ethics in Clinical Trials -- 19. Vaccine Clinical Trials -- 20. Real-World Evidence Studies and Pragmatic Clinical Trials -- 21. Contract Research Organizations - Roles & Responsibilities -- 22. Bioavailability and Bioequivalence Studies -- 23. New Drugs and Clinical trial rules 2019 -- 24. Regulation of healthcare products by the United States Food and Drug Administration and Health Canada -- 25. Regulation of healthcare products by the United States Food and Drug Administration and Health Canada -- 26. Medical Device and Medical Device Regulations -- 27. Off-Label Use of Drugs -- 28. Nonclinical testing methods to assess safety and efficacy of new drugs -- 29. Novel Chemical and Biological Entities in the Past Five Years -- 30. Drug Repurposing -- 31. Specialized Drug Delivery System -- 32. Biologicals and Biosimilars |
| Persistent Identifier |
URN: urn:nbn:de:101:1-2511040309008.132034287371 DOI: 10.1007/978-981-95-1920-0 |
| URL | https://doi.org/10.1007/978-981-95-1920-0 |
| ISBN/Einband/Preis | 978-981-95-1920-0 |
| Sprache(n) | Englisch (eng) |
| DDC-Notation | 615.1 (maschinell ermittelte DDC-Kurznotation) |
| Sachgruppe(n) | 610 Medizin, Gesundheit |
| Online-Zugriff | Archivobjekt öffnen |
Treffer 152 von 28493
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