Handbook of Modern Pharmaceutical Analysis

• Author : Satinder Ahuja,Stephen Scypinski
• Publisher : Elsevier
• Release : 02 August 2001

This book describes the role modern pharmaceutical analysis plays in the development of new drugs. Detailed information is provided as to how the quality of drug products is assured from the point of discovery until the patient uses the drug. Coverage includes state-of-the-art topics such as analytics for combinatorial chemistry and high-throughput screening, formulation development, stability studies, international regulatory aspects and documentation, and future technologies that are likely to impact the field. Emphasis is placed on current, easy-to-follow methods that

• Author : Satinder Ahuja,Stephen Scypinski
• Publisher : Academic Press
• Release : 11 November 2010

Handbook of Modern Pharmaceutical Analysis, Second Edition, synthesizes the complex research and recent changes in the field, while covering the techniques and technology required for today's laboratories. The work integrates strategy, case studies, methodologies, and implications of new regulatory structures, providing complete coverage of quality assurance from the point of discovery to the point of use. Treats pharmaceutical analysis (PA) as an integral partner to the drug development process rather than as a service to it Covers method development, validation,

• Author : Ahuja
• Publisher : Unknown
• Release : 01 January 2005

• Author : Michael W. Dong
• Publisher : John Wiley & Sons
• Release : 06 April 2016

A comprehesive yet concise guide to Modern HPLC Written for practitioners by a practitioner, Modern HPLC for Practicing Scientists is a concise text which presents the most important High-Performance Liquid Chromatography (HPLC) fundamentals, applications, and developments. It describes basic theory and terminology for the novice, and reviews relevant concepts, best practices, and modern trends for the experienced practitioner. Moreover, the book serves well as an updated reference guide for busy laboratory analysts and researchers. Topics covered include: HPLC operation Method

• Author : Manish Thimmaraju
• Publisher : Unknown
• Release : 05 April 2018

The book Practical Instrumental Analysis is a genuine attempt to improve the practical knowledge of Pharm D students. The book is designed as per PCI regulations covering wide spectrum of Instrumental techniques like Spectroscopy, Colorimetric, Chromatography which includes Paper, Thin, Radial, Gradient &Isocratic HPLC, FTIR and Electrochemical analysis.The main objective of this book is to create interest in science of testing Active Pharmaceutical Ingredients and testing the purity in different dosage forms by various instrumental methods of analysis. Salient

• Author : John Bodenhan Taylor,Bernard Testa,D. J. Triggle,Han van de Waterbeemd
• Publisher : Elsevier Science Limited
• Release : 27 September 2021

To be effective a drug must be Absorbed then Distributed to the site of action. It must also be Metabolised and Excreted without any measurable Toxicity (ADMET). This volume examines major ADMET issues, tools to measure these properties in vivo and in vitro and in-silico tools to predict and analyse effects. It concludes with a review of tools that can assist drug discovery in its early development stage. * valuable content available May 2009 as an individual volume * separate volumes will appeal

• Author : Sarwar Beg,Md Saquib Hasnain,Mahfoozur Rahman,Waleed H. Almalki
• Publisher : Academic Press
• Release : 09 January 2021

Handbook of Analytical Quality by Design addresses the steps involved in analytical method development and validation in an effort to avoid quality crises in later stages. The AQbD approach significantly enhances method performance and robustness which are crucial during inter-laboratory studies and also affect the analytical lifecycle of the developed method. Sections cover sample preparation problems and the usefulness of the QbD concept involving Quality Risk Management (QRM), Design of Experiments (DoE) and Multivariate (MVT) Statistical Approaches to solve by

• Author : Jose V. Bonilla,G. Susan Srivatsa
• Publisher : CRC Press
• Release : 23 February 2011

Oligonucleotides represent one of the most significant pharmaceutical breakthroughs in recent years, showing great promise as diagnostic and therapeutic agents for malignant tumors, cardiovascular disease, diabetes, viral infections, and many other degenerative disorders. The Handbook of Analysis of Oligonucleotides and Related Products is an essential reference manual on the practical application of modern and emerging analytical techniques for the analysis of this unique class of compounds. A strong collaboration among thirty leading analytical scientists from around the world, the book

• Author : Anonim
• Publisher : Unknown
• Release : 27 September 2021

Every 3rd issue is a quarterly cumulation.

• Author : NIIR Board
• Publisher : ASIA PACIFIC BUSINESS PRESS Inc.
• Release : 01 January 2004

Drugs and pharmaceutical industry plays a vital role in the economic development of a nation. It is one of the largest and most advanced sectors in the world, acting as a source for various drugs, medicines and their intermediates as well as other pharmaceutical formulations. India has come a long way in this field, from a country importing more than 95% of its requirement of drugs and pharmaceuticals; India now is exporting it even to developed countries. Being the intense knowledge

• Author : Ajit S. Narang,Sherif I.F. Badawy
• Publisher : Academic Press
• Release : 31 August 2018

Handbook of Pharmaceutical Wet Granulation: Theory and Practice in a Quality by Design Paradigm offers a single and comprehensive reference dedicated to all aspects of pharmaceutical wet granulation, taking a holistic approach by combining introductory principles with practical solutions. Chapters are written by international experts across industry, academic and regulatory settings, and cover a wide spectrum of relevant and contemporary wet granulation topics, techniques and processes. The books' focus on process analytical technology, quality by design principles, granulation equipment, modeling,

• Author : Steven H.Y. Wong,Irving Sunshine
• Publisher : CRC Press
• Release : 22 November 2017

Adapting modern advances in analytical techniques to daily laboratory practices challenges many toxicologists, clinical laboratories, and pharmaceutical scientists. The Handbook of Analytical Therapeutic Drug Monitoring and Toxicology helps you keep abreast of the innovative changes that can make your laboratory - and the studies undertaken in it - a success. This volume simplifies your search for appropriate techniques, describes recent contributions from leading investigators, and provides valuable evaluations and advice.

• Author : Roger E. Schirmer
• Publisher : Unknown
• Release : 27 September 1982

• Author : Walkiria S. Schlindwein,Mark Gibson
• Publisher : John Wiley & Sons
• Release : 19 March 2018

A practical guide to Quality by Design for pharmaceutical product development Pharmaceutical Quality by Design: A Practical Approach outlines a new and proven approach to pharmaceutical product development which is now being rolled out across the pharmaceutical industry internationally. Written by experts in the field, the text explores the QbD approach to product development. This innovative approach is based on the application of product and process understanding underpinned by a systematic methodology which can enable pharmaceutical companies to ensure that

• Author : Andrew Davis,Simon E Ward
• Publisher : Royal Society of Chemistry
• Release : 07 July 2015

Drug discovery is a constantly developing and expanding area of research. Developed to provide a comprehensive guide, the Handbook of Medicinal Chemistry covers the past, present and future of the entire drug development process. Highlighting the recent successes and failures in drug discovery, the book helps readers to understand the factors governing modern drug discovery from the initial concept through to a marketed medicine. With chapters covering a wide range of topics from drug discovery processes and optimization, development of