Description

Book Synopsis

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.

Introduction to Basics of Pharmacology and Toxicology

    Product form

    £132.99

    Includes FREE delivery

    RRP £13,999.00 – you save £13,866.01 (99%)

    Order before 4pm today for delivery by Sat 27 Jun 2026.

    A Hardback by Avinash Arivazhahan

    15 in stock

      Trusted by thousands of customers. See 2,385+ Customer Reviews

      View other formats and editions of Introduction to Basics of Pharmacology and Toxicology by Avinash Arivazhahan

      Publisher: Springer
      Publication Date: 11/13/2025
      ISBN13: 9789819519194, 978-9819519194
      ISBN10: 9819519195
      Also in:
      Medical research

      Description

      Book Synopsis

      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.

      Recently viewed products

      © 2026 Book Curl

        • American Express
        • Apple Pay
        • Diners Club
        • Discover
        • Google Pay
        • Maestro
        • Mastercard
        • PayPal
        • Shop Pay
        • Union Pay
        • Visa

        Login

        Forgot your password?

        Don't have an account yet?
        Create account