Drugs and the Pharmaceutical Sciences
About the Book Series
Drugs and the Pharmaceutical Sciences series is designed to enable the pharmaceutical scientist to stay abreast of the changing trends, advances and innovations associated with therapeutic drugs and that area of expertise and interest that has come to be known as the pharmaceutical sciences. The body of knowledge that those working in the pharmaceutical environment have to work with, and master, has been, and continues, to expand at a rapid pace as new scientific approaches, technologies, instrumentations, clinical advances, economic factors and social needs arise and influence the discovery, development, manufacture, commercialization and clinical use of new agents and devices.
Pharmaceutical Computer Systems Validation: Volume 2 - Real Life Case Studies
3rd Edition
Edited
By Guy Wingate
June 14, 2026
Computerized systems play a fundamental role in the development, manufacture and supply of medical treatments. This is the third and thoroughly updated edition of the best-selling book dealing with validation, compliance and software in the pharmaceutical, healthcare and medical device industries. ...
Pharmaceutical Computer Systems Validation: Two Volume Set
3rd Edition
Edited
By Guy Wingate
June 14, 2026
Computerized systems play a fundamental role in the development, manufacture and supply of medical treatments. This is the third and thoroughly updated edition of the best-selling book dealing with validation, compliance and software in the pharmaceutical, healthcare and medical device industries. ...
GMP, GCP and GLP Bundle
1st Edition
Edited
By Graham P. Bunn
May 25, 2026
This bundle brings together three essential books on the USA regulatory requirements for the discovery/development, clinical determination and production/testing of pharmaceutical products: Good Laboratory Practice for Nonclinical Studies, Good Clinical Practices in Pharmaceuticals, and the new ...
Good Manufacturing Practices for Pharmaceuticals
8th Edition
Edited
By Graham P. Bunn
May 25, 2026
This book provides insight into the world of pharmaceutical quality systems and the key elements that must be in place to change the business and organizational dynamics from task-oriented procedure-based cultures to truly integrated quality business systems that are self-detecting and correcting. ...
An Introduction to Generative Drug Discovery
1st Edition
Edited
By Sean Ekins
May 21, 2026
This book describes the state‑of‑the‑art methods and applications for de novo design of drug candidates using generative chemistry models as well as the ethical aspects of this technology. It will provide a foundation for those new to the field as well as those that may already have some experience...
Good Clinical Practices in Pharmaceuticals
1st Edition
Edited
By Graham P. Bunn
May 21, 2026
Good clinical practice (GCP) is a set of internationally recognized ethical and scientific quality requirements that must be followed when designing, conducting, recording, and reporting trials that involve the participation of human subjects. Compliance with GCP assures patients and the public ...
Principles of Research Methodology and Ethics in Pharmaceutical Sciences: An Application Guide for Students and Researchers
1st Edition
Edited
By Vikas Anand Saharan, Hitesh Kulhari, Hemant R Jadhav
May 21, 2026
Pharmaceutical researchers are constantly looking for drug products, drug delivery systems and devices for improving the health of society. A scientific and systematic search for new knowledge requires a thorough understanding of research methods and hypothesis design. This volume presents ...
Nanomedicine and Applications in Cancer: A Complete Guide to Nanomedicine and Cancer Applications
1st Edition
Edited
By Imran Saleem, Ahmed AH Abdellatif
December 18, 2025
Nanomedicine represents a paradigm shift in cancer therapeutics, offering targeted drug delivery, reduced systemic toxicity, and enhanced efficacy. This book provides a detailed and systematic overview of nanomedicine formulations and their diverse applications across the cancer treatment landscape...
GMP Audits in Pharmaceutical and Biotechnology Industries
1st Edition
By Mustafa Edik
August 29, 2025
The fact that good manufacturing practice (GMP) audits in the pharmaceutical and biotechnology industries have to be evaluated, and with very limited resources, has created a gap in this field. The lack of trained and qualified GMP auditors is on the rise in all organizations that are required to ...
Purification of Biotechnological Products: A Focus on Industrial Applications
1st Edition
Edited
By Adalberto Pessoa Jr, Beatriz Vahan Kilikian, Paul Long
August 29, 2025
This outstanding text focuses on providing professionals and students working in the pharmaceutical and biotechnology field with the background necessary for developing of a product or process and with the necessary rigor required by federal regulatory agencies in the pharmaceutical industry. The ...
Molecular Recognition in Pharmacology
1st Edition
By Mikhail Darkhovskiy
May 05, 2025
This unique volume traces the behavior of the drug substance, starting from the initial pre-contact stage, and ending with the formation of the complex. Molecular recognition lies in the foundation of every life form and includes many mysteries. Currently, studies on this topic in pharmacology are ...
Industrial Hygiene in the Pharmaceutical and Consumer Healthcare Industries
1st Edition
By Casey C. Cosner
March 12, 2025
This volume is an update on the use of containment in the pharmaceutical industry and consumer healthcare. It serves to highlight how industrial hygiene acts as a driving force within these industries to reduce the risk of exposure to chemical and physical agents, particularly to powders and dusts,...