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Environmental Monitoring for Cleanrooms and Controlled Environments
ISBN: 9780824723590 / Angielski / Twarda / 230 str. Termin realizacji zamówienia: ok. 5-8 dni roboczych. Spanning every subject of critical importance to the field of environmental monitoring, this guide offers step-by-step guidance on the assessment of air, surfaces, water, action levels, instruments, and procedures in cleanroom facilities. Emphasizing the importance of data gleaned from evaluation and sampling studies, this guide shows how to use this information to reduce contamination risks and provide safe and stable operating conditions for the development of pharmaceutical products. This reference also covers certification/requalification and new ISO standards.
Spanning every subject of critical importance to the field of environmental monitoring, this guide offers step-by-step guidance on the assessment of a...
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930,57 |
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Pharmacogenetics
ISBN: 9780824728847 / Angielski / Twarda / 344 str. Termin realizacji zamówienia: ok. 5-8 dni roboczych. Compiled by leading authorities on the topic, this guide explains how genetic variation contributes to differing patient responses to medicines, including chemotherapy emphasizes how pharmacogenetics will alter the diagnosis, classification, and treatment of common diseases demonstrates the role of pharmacogenetics in the development of patient-tailored medications discusses variability in drug metabolism enzyme pathways The only source on the subject to offer both an overview and a disease-based approach, this reference text spans the wide array of technical, methodological, regulatory, and...
Compiled by leading authorities on the topic, this guide explains how genetic variation contributes to differing patient responses to medicines, inclu...
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930,57 |
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Drug Products for Clinical Trials
ISBN: 9780824754624 / Angielski / Twarda / 432 str. Termin realizacji zamówienia: ok. 5-8 dni roboczych. Addressing issues at the forefront of interest for the Clinical Trial Materials Professional (CTMP), this Second Edition highlights the most critical concepts related to the planning, manufacturing, packaging, labeling, distribution, reconciliation, and quality and regulatory control of clinical trial materials. It offers authoritative chapters by esteemed researchers and consultants in industry on the current and evolving state of clinical supplies operations. Tracking emerging trends and the development of new technologies, this Second Edition helps the CTMP operate effectively in the...
Addressing issues at the forefront of interest for the Clinical Trial Materials Professional (CTMP), this Second Edition highlights the most critical ...
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930,57 |
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Pharmaceutical Dissolution Testing
ISBN: 9780824754679 / Angielski / Twarda / 429 str. Termin realizacji zamówienia: ok. 5-8 dni roboczych. An expertly written source on the devices, systems, and technologies used in the dissolution testing of oral pharmaceutical dosage forms, this reference provides reader-friendly chapters on currently utilized equipment, equipment qualification, consideration of the gastrointestinal physiology in test design, the analysis and interpretation of data and procedure automation -laying the foundation for the creation of appropriate and useful dissolution tests according to the anticipated location and duration of drug release from the dosage form within the gastrointestinal tract.
An expertly written source on the devices, systems, and technologies used in the dissolution testing of oral pharmaceutical dosage forms, this referen...
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930,57 |
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Preformulation in Solid Dosage Form Development
ISBN: 9780824758097 / Angielski / Twarda / 616 str. Termin realizacji zamówienia: ok. 5-8 dni roboczych. During the onset of any clinical trial there are many factors and variables to consider. Funding, time restraints, and regulatory agency guidelines are factors that often influence which variables will be studied, leaving other important information out of the study. Preformulation in Solid Dosage Form Development covers every topic of critical importance to the preformulation stages of drug development. Serving as a handbook or stand-alone reference, this text equips those in academia and the pharmaceutical industry with both basic and applied principles for the... During the onset of any clinical trial there are many factors and variables to consider. Funding, time restraints, and regulatory agency guidelines... |
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930,57 |
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Drug Delivery to the Oral Cavity: Molecules to Market
ISBN: 9780824782931 / Angielski / Twarda / 448 str. Termin realizacji zamówienia: ok. 5-8 dni roboczych. With contributions from recognized authorities in industry, academia, and government, this reference presents the state-of-the-art in the testing, formulation, and clinical evaluation of intraoral drug delivery products-summarizing intraoral dosage forms in various stages of research, as well as products currently on the market.
With contributions from recognized authorities in industry, academia, and government, this reference presents the state-of-the-art in the testing, for...
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930,57 |
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Development of Biopharmaceutical Parenteral Dosage Forms
ISBN: 9780824799816 / Angielski / Twarda / 268 str. Termin realizacji zamówienia: ok. 5-8 dni roboczych. Delineates the appropriate, sequential steps for the formulation of safe, effective, stable, and marketable liquid parenteral biopharmaceutical products--covering fundamentals and essential pathways for each phase as well as its purpose, function, and relation to other stages in the product development process. Written by experts currently involved in state-of-the-art advances in the pharmaceutical drug industry.
Delineates the appropriate, sequential steps for the formulation of safe, effective, stable, and marketable liquid parenteral biopharmaceutical produc...
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930,57 |
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Percutaneous Penetration Enhancers
ISBN: 9780849321528 / Angielski / Twarda / 448 str. Termin realizacji zamówienia: ok. 5-8 dni roboczych. Thoroughly updated, this second edition is the most comprehensive reference on the methods available for the enhancement of percutaneous penetration. The book examines a broad scope of chemical enhancers and various physical methods of enhancement. The range of chemicals discussed is, arguably, unsurpassed anywhere in the literature. This edition contains comprehensive descriptions of the latest techniques and several chapters cover the modern analytical techniques adapted to assess and measure penetration enhancement. New to this volume are chapters addressing penetration retardation,... Thoroughly updated, this second edition is the most comprehensive reference on the methods available for the enhancement of percutaneous penetratio... |
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930,57 |
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The Handbook of C-Arm Fluoroscopy-Guided Spinal Injections
ISBN: 9780849322549 / Angielski / Twarda / 296 str. Termin realizacji zamówienia: ok. 5-8 dni roboczych. For some time now, C-arm fluoroscopy-guided spinal injections have been performed widely for both the diagnosis and management of spinal and paraspinal pain. Despite this common use, many residents and pain fellows do not receive formal training in the anatomy of the vertebral column as it relates to radiographic imaging, nor do they receive any training in fluoroscopic imaging. While books do exist on the subject, they only show the final needle position for spinal injections, and offer very limited instruction. The Handbook of C-Arm Fluoroscopy-Guided Spinal Injections provides...
For some time now, C-arm fluoroscopy-guided spinal injections have been performed widely for both the diagnosis and management of spinal and paraspina...
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930,57 |
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In Vivo MR Techniques in Drug Discovery and Development
ISBN: 9780849330261 / Angielski / Twarda / 604 str. Termin realizacji zamówienia: ok. 5-8 dni roboczych. Imaging technologies are receiving much attention in the pharmaceutical industry because of their potential for accelerating drug discovery and development. Magnetic Resonance Imaging (MRI) is one of the principal imaging modalities because it allows information to be gathered non-invasively. The non-invasiveness of MR strengthens the link between preclinical and clinical pharmaceutical research, contributing to improve the characterization of compound effects in early stages of the discovery process in order to increase the chances of success in later phases of drug development. Edited by a...
Imaging technologies are receiving much attention in the pharmaceutical industry because of their potential for accelerating drug discovery and develo...
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930,57 |
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Understanding Drug Release and Absorption Mechanisms: A Physical and Mathematical Approach
ISBN: 9780849330872 / Angielski / Twarda / 648 str. Termin realizacji zamówienia: ok. 5-8 dni roboczych. Demand for better reliability from drug delivery systems has caused designers and researchers to move away from trial-and-error approaches and toward model-based methods of product development. Developing such models requires cross-disciplinary physical, mathematical, and physiological knowledge. Combining these areas under a single cover, Understanding Drug Release and Absorption Mechanisms builds a firm understanding ofall elements needed to conceive, build, and implement successful models of drug release.
Written by experts with broad industrial and academic experience, this book... Demand for better reliability from drug delivery systems has caused designers and researchers to move away from trial-and-error approaches and toward ...
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930,57 |
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Pharmaceutical Product Development: In Vitro-In Vivo Correlation
ISBN: 9780849338274 / Angielski / Twarda / 224 str. Termin realizacji zamówienia: ok. 5-8 dni roboczych. During the last two decades, the pharmaceutical industry has been under pressure to reduce development costs and the time needed to bring drugs to market in order to maximize return on investment and bring treatments to patients sooner. To meet these ends, pharmaceutical scientists working in the differing areas of pharmacy, pharmaceutics, and pharmacokinetics are collaborating to address physicochemical and biological issues in the early stages of development to avoid problems in later stages. In Vitro-In Vivo Correlation (IVIVC) is a multidisciplinary tool that has been successfully applied...
During the last two decades, the pharmaceutical industry has been under pressure to reduce development costs and the time needed to bring drugs to mar...
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930,57 |
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Pharmaceutical Project Management
ISBN: 9780849340246 / Angielski / Twarda / 282 str. Termin realizacji zamówienia: ok. 5-8 dni roboczych. Encompassing the full spectrum of project management s role and responsibility encountered in the pharmaceutical industry, Pharmaceutical Project Management outlines the key objectives, risks, and challenges of each stage of the pharmaceutical lifecycle, from discovery and preclinical phases through clinical development, manufacturing, registration, and launch. New updated material includes:
Encompassing the full spectrum of project management s role and responsibility encountered in the pharmaceutical industry, Pharmaceutic... |
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Handbook of Human Toxicology
ISBN: 9780849344930 / Angielski / Twarda / 1136 str. Termin realizacji zamówienia: ok. 5-8 dni roboczych. Covering some of the most important topics in modern toxicology, the Handbook of Human Toxicology is a unique and valuable addition to the current literature. It addresses issues, answers questions, and provides data related to. Within each of these five major sections are several carefully selected topics that reflect the current state of human toxicology. From tissue uptake of mercury to the effects of drugs on immune systems, the text provides much-needed information quickly and easily.
Covering some of the most important topics in modern toxicology, the Handbook of Human Toxicology is a unique and valuable addition to the current lit...
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930,57 |
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Dermal Absorption and Toxicity Assessment
ISBN: 9780849375910 / Angielski / Twarda / 678 str. Termin realizacji zamówienia: ok. 5-8 dni roboczych. The source Dermal Absorption and Toxicity Assessment supplies a state-of-the-art overview of the dermal absorption process, and is divided into six well organized sections. Written by internationally recognized experts in the field, this Second Edition is a complete revised and updated text, covering the wide range of methods used to assess skin absorption and the various governmental and industrial programs concerned with skin permeation and toxicity. These include alternative in silico, in vitro, and in vivo strategies to conduct studies for regulatory requirements. To make room for this...
The source Dermal Absorption and Toxicity Assessment supplies a state-of-the-art overview of the dermal absorption process, and is divided into six we...
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930,57 |
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Validation and Qualification in Analytical Laboratories
ISBN: 9780849382673 / Angielski / Twarda / 288 str. Termin realizacji zamówienia: ok. 5-8 dni roboczych. This complete guide and reference explains how to improve product quality while achieving compliance with the world's regulatory standards. It shows how to develop and implement a validation strategy for routine, nonroutine, and standard analytical methods encompassing the entire equipment hardware and software qualification process. It includes examples and templates to help readers through the validation process. In addition to guidelines on the qualification of standards, certified and in-house reference materials, and employee qualification, it covers internal and third-party lab audits...
This complete guide and reference explains how to improve product quality while achieving compliance with the world's regulatory standards. It shows h...
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930,57 |
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Liposome Technology: Entrapment of Drugs and Other Materials Into Liposomes
ISBN: 9780849388286 / Angielski / Twarda / 424 str. Termin realizacji zamówienia: ok. 5-8 dni roboczych. Liposome Technology, Volume II: Entrapment of Drugs and Other Materials into Liposomes, Third Edition is a comprehensively updated and expanded new edition of a classic text in the field. Including step-by-step technical details, Volume II describes procedures for the incorporation of drugs and other materials into liposomes for a variety therapeutics, chosen because of their relevance to current trends in liposome applications or because they represent groups of active pharmaceutical ingredients with similar physical and chemical properties. This source also offers critical discussions of...
Liposome Technology, Volume II: Entrapment of Drugs and Other Materials into Liposomes, Third Edition is a comprehensively updated and expanded new ed...
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930,57 |
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Preparing for FDA Pre-Approval Inspections: A Guide to Regulatory Success, Second Edition
ISBN: 9780849391842 / Angielski / Twarda / 304 str. Termin realizacji zamówienia: ok. 5-8 dni roboczych. This Second Edition is an essential guide to preparing for FDA pre-approval inspections taking into account current trends in FDA expectations and inspection activities, such as the GMPs of the 21st Century, quality systems-based approach to inspections, risk-based inspections, quality by design, process analytical technology, design space, etc. The goal of this book is to help organizations gain rapid regulatory approval. Pharmaceutical Pre-Approval Inspections: A Guide to Regulatory Success, Second Edition: ...This Second Edition is an essential guide to preparing for FDA pre-approval inspections taking into account current trend... |
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930,57 |
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Endotoxins : Pyrogens, LAL Testing and Depyrogenation
ISBN: 9780849393723 / Angielski / Twarda / 419 str. Termin realizacji zamówienia: ok. 5-8 dni roboczych. This source expertly examines the discovery, control, and application of endotoxin form a parenteral manufacturing perspective, including discussioins of assay development, automation, depyrogenation, and the regulation of endotoxin testing by amebocyte lysate(LAL) methods. Completely revised and expanded, this source contains the knowledge necessary to apply endotoxin technologies in the increasingly complex pharmaceutical environment, and offers neew ans state-of-the-art sections on medical devices, regulation standards, validation procedures, and automated system dvelopments.
This source expertly examines the discovery, control, and application of endotoxin form a parenteral manufacturing perspective, including discussioins...
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cena:
930,57 |
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Liposome Technology: Interactions of Liposomes with the Biological Milieu
ISBN: 9780849397257 / Angielski / Twarda / 464 str. Termin realizacji zamówienia: ok. 5-8 dni roboczych. Liposome Technology, Volume III: Interactions of Liposomes with the Biological Milieu, Third Edition, is a comprehensively updated and expanded new edition of a classic text in the field. Including step-by-step technical details, Volume III describes technologies for yielding liposomes that can function in a targeted fashion, and highlights methods for studying the interaction of liposomes within the biological environment to be applied in the detection, therapy, or prevention of disease. This source also offers critical discussions of the methodologies of each technology described so that...
Liposome Technology, Volume III: Interactions of Liposomes with the Biological Milieu, Third Edition, is a comprehensively updated and expanded new ed...
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cena:
930,57 |