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Biological Reactive Intermediates IV
The finding that chemicals can be metabolically activated to yield reactive chemical species capable of covalently binding to cellular macromolecules and the concept that these reactions could initiate toxicological and carcinogenic events stimulated a meeting by a small group of toxicologists at the University of Turku, in Finland, in 1975 (Jollow et al. , 1977). The growing interest in this field of research led to subsequent symposia at the University of Surrey, in England in 1980 (Snyder et al. , 1982), and the University of Maryland in the U. S. A. in 1985 (Kocsis et al. , 1986). The Fourth International Symposium on Biological Reactive Intermediates was hosted by the Center for Toxicol...
Nitric Oxide
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ICH Quality Guidelines
Examining the implications and practical implementation of multi-disciplinary International Conference on Harmonization (ICH) topics, this book gives an integrated view of how the guidelines inform drug development strategic planning and decision-making. • Addresses a consistent need for interpretation, training, and implementation examples of ICH guidelines via case studies • Offers a primary reference point for practitioners addressing the dual challenge of interpretation and practical implementation of ICH guidelines • Uses case studies to help readers understand and apply ICH guidelines • Provides valuable insights into guidelines development, with chapters by authors involved in generating or with experience implementing the guidelines • Includes coverage of stability testing, analytical method validation, impurities, biotechnology drugs and products, and good manufacturing practice (GMP)
Process Validation in Manufacturing of Biopharmaceuticals
The fourth edition of Process Validation in Manufacturing of Biopharmaceuticals is a practical and comprehensive resource illustrating the different approaches for successful validation of biopharmaceutical processes. A pivotal text in its field, this new edition provides guidelines and current practices, contains industrial case studies, and is expanded to include in-depth analysis of the new Process Validation (PV) guidance from the US FDA. Key Features: Offers readers a thorough understanding of the key concepts that form the basis of a good process validation program for biopharmaceuticals. Includes case studies from the various industry leaders that demonstrate application of these conc...
Evolution and Eschatology
The genome revolution of the last twenty years has changed biology forever. It has provided stunning insights into the evolution of species (such as ours) and the development of new functional capabilities (such as placenta, brain, and immune networks). We are learning how genes make a human animal―but that loving relationships with others are required to make a human person. Random mutations, filtered by directing order, underlie evolutionary development, but also cause diseases such as cancer. We are wont to question God when faced with devastating natural and moral evils. But deeply embedded in the biblical story we encounter a Creator who has always purposed to deal with the evils of a freely operating world by extirpating them through Jesus of Nazareth, who is God incarnate.
Inside OUT
Inside OUT: Human Health and the Air-Conditioning Era focuses on the enclosed environment of fully conditioned buildings, revealing a unique ecosystem with broad implications for human life and a rapidly expanding global footprint. Emphasizing the interconnections between buildings and human health, equity, and environmental sustainability, it presents an interdisciplinary, holistic analysis of the social, behavioral, and technological issues of indoor space. Over the 20th century, advances in mechanical conditioning technologies led to the dispersion and international dominance of the sealed building envelope, which casually and progressively disconnected buildings and their occupants from ...
Process Validation in Manufacturing of Biopharmaceuticals, Third Edition
Process Validation in Manufacturing of Biopharmaceuticals, Third Edition delves into the key aspects and current practices of process validation. It includes discussion on the final version of the FDA 2011 Guidance for Industry on Process Validation Principles and Practices, commonly referred to as the Process Validation Guidance or PVG, issued in final form on January 24, 2011. The book also provides guidelines and current practices, as well as industrial case studies illustrating the different approaches that can be taken for successful validation of biopharmaceutical processes. Case studies include Process validation for membrane chromatography Leveraging multivariate analysis tools to qu...
Cell Culture
Cell culture is one of the major tools used in cellular and molecular biology, delivering an excellent model for studying the normal physiology and biochemistry of cells. This book covers some advanced aspects in cell culture methodologies. The book has four sections discussing different types of cell culture models, including 3D cell culture techniques, their advantages, and limitations in comparison to traditional 2D culturing; cell viability, autophagy, in vitro toxicity tests and live cell imaging; stem cell culture for cell-based therapeutics; and specific applications and methodologies for hybrid cell lines and cancer models. This book provides a comprehensive overview of some of the advanced cell culture methodologies and applications. It serves as a valuable source for scientists, researchers, clinicians and students.
