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.
Edited
By Sean Ekins
January 30, 2025
This timely volume describes the state of the art methods and applications for de novo design of drug candidates using generative chemistry models as well as ethical aspects of this technology. The authors discuss democratization of computational drug discovery; tight integration with experimental ...
Edited
By Graham P. Bunn
December 02, 2024
Good clinical practice ( GCP ) is a set of internationally-recognised 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 ...
Edited
By Ajit S. Narang, Atul Dubey
October 09, 2024
Continuous manufacturing of pharmaceuticals, including aspects of modern process development is highlighted in this book with both the ‘why’ and the ‘how’, emphasizing process modeling and process analytical technologies. Presenting specific case studies and drawing upon extensive experience from ...
Edited
By Dimitrios Lamprou
October 09, 2024
This book details the advances in drug discovery and delivery and the present need for emerging technologies. Throughout the text new micro and nanofabrication techniques are described, including methods such as electrohydrodynamic processes, additive manufacturing, and microfluidics, which have ...
Edited
By Yashwant Pathak
October 09, 2024
Gene delivery is a transport of genes of therapeutic values into the chromosomes of the cells or tissues which can be targeted to replace the faulty genes. In last two decades lot of research efforts are dedicated to gene delivery for therapeutic applications. Today gene therapy is promising ...
Edited
By Graham P. Bunn
October 09, 2024
The GLP regulations have been enacted since 1978 and are currently under a proposed FDA amendment to revise terminology and accommodate other changes relating to advances in technology related to the industry. This book provides a unique opportunity to access interpretation of the 21CFR58 ...
Edited
By Joseph P. Stalder
October 09, 2024
Project managers in drug development are the driving force behind the coordination of efforts. This book provides a practical reference for project managers in the pharmaceutical and biotech drug development industry, with the goal of assisting in creating an efficient and effective team structure ...
Edited
By Vikas Anand Saharan, Hitesh Kulhari, Hemant R Jadhav
August 30, 2024
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 ...
Edited
By Yashwant Pathak
August 26, 2024
This unique volume in our Drugs and Pharmaceutical Sciences series covers the development of gene therapy today, the technology involved, clinical applications of siRNA, non-viral vector-based mRNA delivery using nanotechnology, and RNA based vaccines for treating the infectious diseases. It also ...
By Mustafa Edik
June 28, 2024
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 ...
Edited
By Adalberto Pessoa, Beatriz Vahan Kilikian, Paul Frederick Long
May 23, 2024
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 ...
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 ...