Pharmaceutical chemistry and technology

This book addresses the resurgence of interest in the rediscovery of ethnomedicinal plants as a source of potential ethnomedicines.

This book addresses the resurgence of interest in the rediscovery of ethnomedicinal plants as a source of potential ethnomedicines.

Algal and sustainable technologies: Bioenergy, Nannotechnology and Green chemistry is an interdisciplinary overview of the world's major problems; water scarcity, clean environment and energy and their sustenance remedy measures using microalgae.

Algal and sustainable technologies: Bioenergy, Nannotechnology and Green chemistry is an interdisciplinary overview of the world's major problems; water scarcity, clean environment and energy and their sustenance remedy measures using microalgae.

Genetic toxicology is considered to be an important assessment tool as there is genetic impact of artificial chemicals.

Genetic toxicology is considered to be an important assessment tool as there is genetic impact of artificial chemicals.

With a high diversity of vegetation in Iran, over 8000 plant species are in existence.

With a high diversity of vegetation in Iran, over 8000 plant species are in existence.

The demand for medicinal plants is increasing, and this leads to unscrupulous collection from the wild and adulteration of supplies.

The demand for medicinal plants is increasing, and this leads to unscrupulous collection from the wild and adulteration of supplies.

PREFACE TO THE SECOND EDITIONThe need for a thorough understanding of medical terminology has not diminished in the least for pharmacists and other health care practitioners in the five years between the publication of the first edition of this book and this second edition.

PREFACE TO THE SECOND EDITIONThe need for a thorough understanding of medical terminology has not diminished in the least for pharmacists and other health care practitioners in the five years between the publication of the first edition of this book and this second edition.

Asceptic Pharmaceutical Manufacturing II explores the sophisticated technology, developments, and applications that allow aseptic processing to approach the sterility levels achieved with terminal sterilization.

In this book, recognized industry experts and regulatory inspectors from the world's pharmaceutical manufacturing regions provide stability requirements in all the major markets and discuss all aspects of stability testing and biotechnology.

Of all the audit functions faced by QA, software auditing is probably the most difficult because of the need to know and understand the intricacies of the processes being audited.

In this unique book, experts describe practices applicable to the large-scale processing of biotechnological products.

The first work of its kind, The History of Medications for Women: Materia medica woman is a richly detailed, far-ranging illustrated history of medications for women in all the great cultures and civilizations, from ancient times to the present.

This research level reference book has been co-written by Enrico Drioli, perhaps one of the world's best known researchers into membrane technology.

At the last Annual Representative Meeting of the British Medical Association a motion was passed that `certain additional cannabinoids should be legalized for wider medicinal use.

Learn how international governments have committed themselves to improving access to quality health care!

Marketing to Pharmacists: Understanding Their Role and Influence will help pharmaceutical marketers better understand pharmaceutical practice in order to develop better relationships with pharmacists and effectively market products.

This book exploits an understanding of disease pathogenesis by applying a variety of biological agents to therapy.

This book focuses on the quantitative structure-activity relationship of the disposition and activities of various pharmacological groups.

An important new collection of clinical and preclinical reports on genetic therapy, this book describes illustrative examples of diseases in which gene-based interventions are presently plausible, and presents case studies of current research using both synthetic oligonucleotides and biological vectors.

This book focuses on statistical methods which impinge more or less directly on the decisions that are made during the course of pharmaceutical and agro-chemical research, considering the four decision-making areas.

This book examines the sequence of events and methodology in the industrial clinical research process; a reference for multidisciplinary personnel.

Stressing the theory involved in formulating suspensions, emulsions, and colloidal drug products, this Second Edition of a well-received reference test highlights typical formulations, the avoidance of formulation pitfalls, and compliance with established regulatory principles.

A practical guide for chemists in the pharmaceutical industry to making automated analyses of drugs that will meet the standards of regulatory agencies.

Presenting all preclinical and clinical information available on genetically engineered toxins, this unique, single-source reference provides the most up-to-date methods and practical examples for conducting clinical studies in toxin molecular biology.

This book is the first to provide both a broad overview of the current methodologies being applied to drug design and in-depth analyses of progress in specific fields.

This textbook integrates basic research and clinical aspects underlying the most recent results in those malignant diseases where progress is most effective.

At the last Annual Representative Meeting of the British Medical Association a motion was passed that `certain additional cannabinoids should be legalized for wider medicinal use.

This research level reference book has been co-written by Enrico Drioli, perhaps one of the world's best known researchers into membrane technology.

Asceptic Pharmaceutical Manufacturing II explores the sophisticated technology, developments, and applications that allow aseptic processing to approach the sterility levels achieved with terminal sterilization.

In this book, recognized industry experts and regulatory inspectors from the world's pharmaceutical manufacturing regions provide stability requirements in all the major markets and discuss all aspects of stability testing and biotechnology.

Of all the audit functions faced by QA, software auditing is probably the most difficult because of the need to know and understand the intricacies of the processes being audited.

In this unique book, experts describe practices applicable to the large-scale processing of biotechnological products.

The first work of its kind, The History of Medications for Women: Materia medica woman is a richly detailed, far-ranging illustrated history of medications for women in all the great cultures and civilizations, from ancient times to the present.

Learn how international governments have committed themselves to improving access to quality health care!

Marketing to Pharmacists: Understanding Their Role and Influence will help pharmaceutical marketers better understand pharmaceutical practice in order to develop better relationships with pharmacists and effectively market products.

An important new collection of clinical and preclinical reports on genetic therapy, this book describes illustrative examples of diseases in which gene-based interventions are presently plausible, and presents case studies of current research using both synthetic oligonucleotides and biological vectors.

This book exploits an understanding of disease pathogenesis by applying a variety of biological agents to therapy.

This book serves as a formulation and processing guide during the development of pelletized dosage forms.

This book focuses on statistical methods which impinge more or less directly on the decisions that are made during the course of pharmaceutical and agro-chemical research, considering the four decision-making areas.

This book examines the sequence of events and methodology in the industrial clinical research process; a reference for multidisciplinary personnel.

Stressing the theory involved in formulating suspensions, emulsions, and colloidal drug products, this Second Edition of a well-received reference test highlights typical formulations, the avoidance of formulation pitfalls, and compliance with established regulatory principles.

A practical guide for chemists in the pharmaceutical industry to making automated analyses of drugs that will meet the standards of regulatory agencies.

Presenting all preclinical and clinical information available on genetically engineered toxins, this unique, single-source reference provides the most up-to-date methods and practical examples for conducting clinical studies in toxin molecular biology.

This book focuses on the quantitative structure-activity relationship of the disposition and activities of various pharmacological groups.

This textbook integrates basic research and clinical aspects underlying the most recent results in those malignant diseases where progress is most effective.