Dosage Forms, Formulation Developments and Regulations, Volume One in the Recent and Future Trends in Pharmaceutics series, explores aspects of pharmaceutics, with an original approach focused on technology, novelties and future trends in the field. The book discusses the most recent developments in pharmaceutical preformulation and formulation studies, biopharmaceutics and novel pharmaceutical formulations, regulatory affairs, and good manufacturing practices. Exciting areas such as formulation strategies, optimization techniques, the biopharmaceutical classification system, and pharmaceutical aerosols are included.
The field of pharmaceutics is highly dynamic and rapidly expanding day-by-day, so it demands a variety of amplified efforts for designing and developing pharmaceutical processes and formulation strategies. This is an essential reference for researchers in academia and industry as well as advanced graduate students in pharmaceutics.
1. Chapter 2 : Introduction to different types of dosage forms and commonly used excipients - p. Page 48 2. Chapter 3 : Pharmacopoeias, national formulary and extra pharmacopoeia - p. Page 81 3. Chapter 4 : Regulatory affairs: historical overview, authorities, and role in drug approval - p. Page 96 4. Chapter 5 : Introduction to intellectual property rights and drug patents - p. Page 137 5. Chapter 6 : Introduction to pharmaceutical validation - p. Page 150 6. Chapter 7 : Design of dosage forms: influences of anatomy and administration routes - p. Page 178 7. Chapter 8 : Formulation strategies to improve the bioavailability of poorly absorbed drugs - p. Page 215 8. Chapter 9 : Optimization techniques in pharmaceutical formulation and processing - p. Page 245 9. Chapter 10 : Pharmaceutical product development: a “quality by design” (QbD) approach - p. Page 278 10. Chapter 11 : Pharmaceutical excipients - p. Page 308 11. Chapter 12 : Pharmaceutical calculations - p. Page 340 12. Chapter 13 : Preformulation considerations in pharmaceutical formulation process - p. Page 391 13. Chapter 14 : Biopharmaceutical Classification System: a strategic tool in pharmaceutical formulation - p. Page 429 14. Chapter 15 : Technology development and transfer in pharmaceutical product development - p. Page 466 15. Chapter 16 : Recent developments in pharmaceutical liquids - p. Page 491 16. Chapter 17 : Advances in semisolid dosage form - p. Page 515 17. Chapter 18 : Pharmaceutical sterilization - p. Page 538 18. Chapter 19 : Pharmaceutical sterile formulations - p. Page 571 19. Chapter 20 : Dermatological formulations - p. Page 609 20. Chapter 21 : Pharmaceutical aerosols - p. Page 639 21. Chapter 22 : Pharmaceutical packaging: recent trends and challenges - p. Page 661 22. Index - p. Page 683
Dosage Forms, Formulation Developments and Regulations, Volume One in the Recent and Future Trends in Pharmaceutics series, explores aspects of pharmaceutics, with an original approach focused on technology, novelties and future trends in the field. The book discusses the most recent developments in pharmaceutical preformulation and formulation studies, biopharmaceutics and novel pharmaceutical formulations, regulatory affairs, and good manufacturing practices. Exciting areas such as formulation strategies, optimization techniques, the biopharmaceutical classification system, and pharmaceutical aerosols are included.
The field of pharmaceutics is highly dynamic and rapidly expanding day-by-day, so it demands a variety of amplified efforts for designing and developing pharmaceutical processes and formulation strategies. This is an essential reference for researchers in academia and industry as well as advanced graduate students in pharmaceutics.
1. Chapter 2 : Introduction to different types of dosage forms and commonly used excipients - p. Page 48 2. Chapter 3 : Pharmacopoeias, national formulary and extra pharmacopoeia - p. Page 81 3. Chapter 4 : Regulatory affairs: historical overview, authorities, and role in drug approval - p. Page 96 4. Chapter 5 : Introduction to intellectual property rights and drug patents - p. Page 137 5. Chapter 6 : Introduction to pharmaceutical validation - p. Page 150 6. Chapter 7 : Design of dosage forms: influences of anatomy and administration routes - p. Page 178 7. Chapter 8 : Formulation strategies to improve the bioavailability of poorly absorbed drugs - p. Page 215 8. Chapter 9 : Optimization techniques in pharmaceutical formulation and processing - p. Page 245 9. Chapter 10 : Pharmaceutical product development: a “quality by design” (QbD) approach - p. Page 278 10. Chapter 11 : Pharmaceutical excipients - p. Page 308 11. Chapter 12 : Pharmaceutical calculations - p. Page 340 12. Chapter 13 : Preformulation considerations in pharmaceutical formulation process - p. Page 391 13. Chapter 14 : Biopharmaceutical Classification System: a strategic tool in pharmaceutical formulation - p. Page 429 14. Chapter 15 : Technology development and transfer in pharmaceutical product development - p. Page 466 15. Chapter 16 : Recent developments in pharmaceutical liquids - p. Page 491 16. Chapter 17 : Advances in semisolid dosage form - p. Page 515 17. Chapter 18 : Pharmaceutical sterilization - p. Page 538 18. Chapter 19 : Pharmaceutical sterile formulations - p. Page 571 19. Chapter 20 : Dermatological formulations - p. Page 609 20. Chapter 21 : Pharmaceutical aerosols - p. Page 639 21. Chapter 22 : Pharmaceutical packaging: recent trends and challenges - p. Page 661 22. Index - p. Page 683
