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The Future of Pharmaceutical Product Development and Research. Advances in Pharmaceutical Product Development and Research

  • ID: 4720866
  • Book
  • August 2020
  • Region: Global
  • 575 Pages
  • Elsevier Science and Technology
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The Future of Pharmaceutical Product Development and Research 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 covers 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 trials
  • Outlines how to ensure an environment that follows Good Manufacturing Practice (GMP)
  • Examines recent developments and suggests future directions for drug production methods and techniques
Note: Product cover images may vary from those shown
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1. New Drugs: Discovery and Development
2. Orphan Drugs
3. Recent advances in Ophthalmic drug delivery
4. Drug Targeting Technology: Physical- Chemical- Biological approaches
5. Radiopharmaceuticals: Chemistry and Pharmacology
6. Biomaterials in tissue engineering and artificial organs
7. Biodegradable block copolymers & their applications for drug delivery
8. Regulatory perspectives of medical devices
9. Recent advances in drug solubilization: Existing strategies and future research directions 
10. Achieving Sterility in biomedical and Pharmaceutical Products
11. Medical device safety and risk management
12. cGMP Quality Principles and Quality system requirements for Medical Devices
13. Governmental regulation for medical devices
14. 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 screening
19. Excipient Toxicity and Safety
20. Pharmacological screening models for therapeutics
21. Correlation between in-vitro and in-vivo screens: Special emphasis on cell-based assay, biochemical assay, radioligand binding assay
Note: Product cover images may vary from those shown
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