The Future of Pharmaceutical Product Development and Research

The Future of Pharmaceutical Product Development and Research

Tekade, Rakesh K.

182,00 €(IVA inc.)

Recent Pharmaceutical Advancements examines the latest developments in the pharmaceutical sciences, also highlighting key developments, research and future opportunities. Written by experts in the field, this volume in the Advances in Pharmaceutical Product Development and Research series deepens our understanding of the product development phase of drug discovery and drug development. Each chapter delves into a particular aspect of this field to cover the fundamental principles, advanced methodologies and technologies employed by pharmaceutical scientists, researchers and the pharmaceutical industry. The book focuses on excipients, radiopharmaceuticals, and how manufacturing should be conducted in an environment that follows Good Manufacturing Practice (GMP) guidelines. Researchers and students will find this book to be a comprehensive resource for those working in, and studying, pharmaceuticals, cosmetics, biotechnology, foods, and related industries. Provides an overview of practical information for clinical trialsOutlines how to ensure an environment that follows Good Manufacturing Practice (GMP)Examines recent developments and suggests future directions for drug production methods and techniques INDICE: 1. New Drugs: Discovery and Development2. Orphan Drugs3. Recent advances in Ophthalmic drug delivery4. Drug Targeting Technology: Physical- Chemical- Biological approaches5. Radiopharmaceuticals: Chemistry and Pharmacology6. Biomaterials in tissue engineering and artificial organs 7. Biodegradable block copolymers & their applications for drug delivery8. Regulatory perspectives of medical devices 9. Recent advances in drug solubilization: Existing strategies and future research directions  10. Achieving Sterility in biomedical and Pharmaceutical Products11. Medical device safety and risk management12. cGMP Quality Principles and Quality system requirements for Medical Devices13. Governmental regulation for medical devices14. Storage considerations for medical devices; implications on material content 15. Clinical Trial Design for pharmaceuticals and Medical Devices 16. Economic aspects of controlled drug delivery devices 17. Oligonucleotides and gene delivery 18. General principles of pharmacological screening19. Excipient Toxicity and Safety20. Pharmacological screening models for therapeutics21. Correlation between in-vitro and in-vivo screens: Special emphasis on cell-based assay, biochemical assay, radioligand binding assay

  • ISBN: 978-0-12-814455-8
  • Editorial: Academic Press
  • Encuadernacion: Cartoné
  • Páginas: 575
  • Fecha Publicación: 01/06/2019
  • Nº Volúmenes: 1
  • Idioma: Inglés