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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.

90 Series Titles


Handbook of Pharmaceutical Granulation Technology

Handbook of Pharmaceutical Granulation Technology

4th Edition

Edited By Dilip M. Parikh
January 29, 2024

This fully revised edition of Handbook of Pharmaceutical Granulation Technology covers the rapid advances in the science of agglomeration,  process control, process modelling, scale-up, emerging particle engineering technologies, along with current regulatory changes presented by some of the ...

Percutaneous Absorption Drugs, Cosmetics, Mechanisms, Methods

Percutaneous Absorption: Drugs, Cosmetics, Mechanisms, Methods

5th Edition

Edited By Nina Dragićević, Howard Maibach
January 29, 2024

Updating and expanding the scope of topics covered in the previous edition, Percutaneous Absorption: Drugs, Cosmetics, Mechanisms, Methods, Fifth Edition supplies new chapters on topics currently impacting the field including cutaneous metabolism, skin contamination, exposure to protein allergens, ...

Filtration and Purification in the Biopharmaceutical Industry, Third Edition

Filtration and Purification in the Biopharmaceutical Industry, Third Edition

3rd Edition

Edited By Maik W. Jornitz
June 13, 2022

Since sterile filtration and purification steps are becoming more prevalent and critical within medicinal drug manufacturing, the third edition of Filtration and Purification in the Biopharmaceutical Industry greatly expands its focus with extensive new material on the critical role of purification...

Biotechnology the Science, the Products, the Government, the Business

Biotechnology: the Science, the Products, the Government, the Business

1st Edition

By Ronald P. Evens
December 13, 2021

The over-riding premise for biotechnology in this book is bringing novel products to market to substantially advance patient care and disease mitigation. Biotechnology, over its relatively brief existence of 40 years, has experienced a mercurial growth. The vast educational need for biotechnology ...

Good Manufacturing Practices for Pharmaceuticals, Seventh Edition

Good Manufacturing Practices for Pharmaceuticals, Seventh Edition

7th Edition

Edited By Graham P. Bunn
September 30, 2021

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. ...

Aqueous Polymeric Coatings for Pharmaceutical Dosage Forms

Aqueous Polymeric Coatings for Pharmaceutical Dosage Forms

4th Edition

Edited By Linda A. Felton
December 18, 2020

Aqueous-based film coating has become routine in the pharmaceutical industry. This process eliminates the use of organic solvents and thus avoids economic, environmental, and toxicological issues related to residual solvents and solvent recovery. Aqueous-based coating, however, is complex and many ...

Biosimilar Drug Product Development

Biosimilar Drug Product Development

1st Edition

Edited By Laszlo Endrenyi, Dr. Paul Declerck, Shein-Chung Chow
June 30, 2020

When a biological drug patent expires, alternative biosimilar products are developed. The development of biosimilar products is complicated and involves numerous considerations and steps. The assessment of biosimilarity and interchangeability is also complicated and difficult. Biosimilar Drug ...

Pharmaceutical Experimental Design

Pharmaceutical Experimental Design

1st Edition

By Gareth A. Lewis, Didier Mathieu, Roger Phan-Tan-Luu
December 02, 2019

This useful reference describes the statistical planning and design of pharmaceutical experiments, covering all stages in the development process-including preformulation, formulation, process study and optimization, scale-up, and robust process and formulation development.Shows how to overcome ...

Proteins and Peptides Pharmacokinetic, Pharmacodynamic, and Metabolic Outcomes

Proteins and Peptides: Pharmacokinetic, Pharmacodynamic, and Metabolic Outcomes

1st Edition

Edited By Randall J. Mrsny, Ann Daugherty
October 10, 2019

Addressing the increased use of protein and peptide candidates as treatments for previously untreatable diseases, this comprehensive and progressive source provides the reader with a roadmap to an increased understanding of issues critical for successfully developing a protein or peptide ...

Development and Formulation of Veterinary Dosage Forms

Development and Formulation of Veterinary Dosage Forms

2nd Edition

By Gregory E. Hardee, J. Desmond Baggo
June 19, 2019

This up-to-the-minute Second Edition of an incomparable resource describes in detail the bases for developing dosage forms for use in animals-highlighting the data necessary to meet regulatory approval.Demonstrates the successful characterization, control, and registration of new veterinary ...

Novel Drug Delivery Systems

Novel Drug Delivery Systems

2nd Edition

By Yie Chien
June 19, 2019

A comprehensive treatment of the science, technology, and regulation of rate-controlled administration of therapeutic agents, with coverage of the basic concepts, fundamental principles, biomedical rationales, and potential applications. This revised and updated edition (first in 1982) incorporates...

The Pharmaceutical Regulatory Process

The Pharmaceutical Regulatory Process

2nd Edition

Edited By Ira R. Berry, Robert P. Martin
June 07, 2019

This Second Edition examines the mechanisms and means to establish regulatory compliance for pharmaceutical products and company practices. It focuses on major legislative revisions that impact requirements for drug safety reviews, product regulatory approvals, and marketing practices. Written by ...

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