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Pharmaceutical and Clinical Calculations
ISBN: 9781566768122 / Angielski / Twarda / 396 str. Termin realizacji zamówienia: ok. 5-8 dni roboczych. Pharmaceutical and clinical calculations are critical to the delivery of safe, effective, and competent patient care and professional practice. Pharmaceutical and Clinical Calculations, Second Edition addresses this crucial component, while emphasizing contemporary pharmacy practices. Presenting the information in a well-organized and easy-to-understand manner, the authors explain the principles of clinical calculations involving dose and dosing regimens in patients with impaired organ functions, aminoglycoside therapy, pediatric and geriatric dosing, and radiopharmaceuticals with appropriate...
Pharmaceutical and clinical calculations are critical to the delivery of safe, effective, and competent patient care and professional practice. Pharma...
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cena:
907,73 zł |
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Pharmacokinetic Principles of Dosing Adjustments: Understanding the Basics
ISBN: 9781566768993 / Angielski / Miękka / 272 str. Termin realizacji zamówienia: ok. 5-8 dni roboczych. This book has evolved over the last twenty years from a cumulative effort to develop a professional course in pharmacokinetics that would assist future practitioners in therapeutic decision making. As practicing pharmacists become more involved with patient advising, it becomes apparent that clinicians will be required to make dosing adjustments for certain drugs. This will become increasingly more likely as pharmacy practitioners have access to patient information that requires careful attention to dose and dosing interval, which in turn correlates to various pharmacokinetic parameters such...
This book has evolved over the last twenty years from a cumulative effort to develop a professional course in pharmacokinetics that would assist futur...
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cena:
570,57 zł |
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Essentials of Pharmacy Law
ISBN: 9781566769181 / Angielski / Miękka / 136 str. Termin realizacji zamówienia: ok. 5-8 dni roboczych. This book examines the laws relating to the practice of pharmacy and the regulation and control of drugs. Written by a practicing pharmacist in clear, accessible, contemporary prose, this user-friendly text deals largely with federal law. Case studies and review questions make for easy reading and aid in comprehension. Essentials of Pharmacy Law will be extremely useful to senior pharmacy students preparing for the Multi-State Jurisprudence Exam (MJPE). It also serves as a valuable reference for pharmacy students, practicing pharmacists seeking licensure by reciprocity and/or preparing for...
This book examines the laws relating to the practice of pharmacy and the regulation and control of drugs. Written by a practicing pharmacist in clear,...
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cena:
388,97 zł |
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Pharmaceutical Care: Insights from Community Pharmacists
ISBN: 9781566769532 / Angielski / Twarda / 190 str. Termin realizacji zamówienia: ok. 5-8 dni roboczych. Pharmacy is the nation's third largest health profession, with nearly 200,000 licensed pharmacists in the United States and 125,000 practicing in community pharmacies. It is in community settings where pharmaceutical care will be judged, accepted, and ultimately paid for. Pharmaceutical Care: Insights from Community Pharmacists introduces the conceptual framework for pharmaceutical care. The authors show you how to apply economic, business, and societal models to better understand it, and they look at the trends in healthcare that drive it.
Vignettes and interviews are the real strength... Pharmacy is the nation's third largest health profession, with nearly 200,000 licensed pharmacists in the United States and 125,000 practicing in comm...
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cena:
570,57 zł |
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Clin-Alert 2000
ISBN: 9781566769624 / Angielski / Twarda / 427 str. Termin realizacji zamówienia: ok. 5-8 dni roboczych. Complete, Authoritative, Unrivaled Collection
Clin-Alert, long established as the pre-eminent source of adverse drug reaction/interaction, now brings you Clin-Alert 2000. Presented in a quick reference format, Clin-Alert 2000 allows very easy access by drug class for comparison reports. Pharmacological classes are arranged based on a modified AHFS Therapeutic Classification Code System AND include the addition of a comprehensive section on alternative/herbal medicines. Complete, Authoritative, Unrivaled Collection
Clin-Alert, long established as the pre-eminent source of adverse drug reaction/interaction, now brin... |
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1063,34 zł |
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Handbook of Assay Development in Drug Discovery
ISBN: 9781574444711 / Angielski / Twarda / 488 str. Termin realizacji zamówienia: ok. 5-8 dni roboczych. Book Description With multiwell assays for drug discovery becoming a staple of the scientific community, the Handbook of Assay Development in Drug Discovery provides general guidelines and specific examples of each assay system. It includes radiometric assays, fluorescent-based assays, and reporter assays for such targets as kinases, proteases, nuclear receptors, and GPCRs. It presents descriptions of methods, exact protocols used to perform such methods, and troubleshooting tools. Featuring contributions from assay developers in the pharmaceutical industry as well as the vendor community,...
Book Description With multiwell assays for drug discovery becoming a staple of the scientific community, the Handbook of Assay Development in Drug Dis...
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cena:
1089,27 zł |
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Dose Optimization in Drug Development
ISBN: 9781574448085 / Angielski / Twarda / 320 str. Termin realizacji zamówienia: ok. 5-8 dni roboczych. This reference provides a concise overview of the key principles in dose selection and optimization and demonstrates applicability to recent successful new drug applications. Compiling key issues and current research on safety, efficacy, and clinical pharmacology, and PK-PD, this volume critically highlights the multidisciplinary nature of drug development and spans the fields of pharmacokinetics, clinical pharmacology, biostatistics, and experimental medicine.
This reference provides a concise overview of the key principles in dose selection and optimization and demonstrates applicability to recent successfu...
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cena:
959,60 zł |
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Biotechnology and Biopharmaceutical Manufacturing, Processing, and Preservation
ISBN: 9781574910162 / Angielski / Twarda / 404 str. Termin realizacji zamówienia: ok. 5-8 dni roboczych. In this volume, experts describe practices applicable to the large-scale processing of biotechnological products. Beginning with processing and bulk storage preservation techniques, the book provides strategies for improving efficiency of process campaigns of multiple products and manufacturing facilities for such processing techniques. Large-scale chromatography for the purification of biomolecules in manufacturing and lyophilization of protein pharmaceuticals are discussed. Includes a case study on blow-fill-seal processing technology and a chapter on economic and cost factors for...
In this volume, experts describe practices applicable to the large-scale processing of biotechnological products. Beginning with processing and bulk s...
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cena:
1685,78 zł |
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Clinical Development: Strategic, Pre-Clinical, and Regulatory Issues
ISBN: 9781574910285 / Angielski / Twarda / 248 str. Termin realizacji zamówienia: ok. 5-8 dni roboczych. Everyone involved in pre-clinical, clinical, formulation, development and regulatory affairs will find Clinical Development a valuable resource. The book provides expert advice on ways to reduce delays and lost market opportunities, minimize development time, better understand the process and regulatory requirements, and plan and analyze clinical development and testing programs. The author combines text, graphs, and charts to show how a company moves a product through the complex process from discovery to market. The result is a complete analysis of the drug development process in...
Everyone involved in pre-clinical, clinical, formulation, development and regulatory affairs will find Clinical Development a valuable resource. The b...
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cena:
778,05 zł |
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Good Pharmaceutical Freeze-Drying Practice
ISBN: 9781574910315 / Angielski / Twarda / 320 str. Termin realizacji zamówienia: ok. 5-8 dni roboczych. This text is devoted to pharmaceutical freeze-drying in all its forms and in all its technological variations. Whether you freeze-dry nonsterile tablets or you lyophilize injectables, this book covers all the technological and regulatory requirements. Written by a panel of leading practitioners in the pharmaceutical industry -- production experts, regulatory inspectors, technical consultants, and equipment suppliers -- the information is relevant, usable, and timely. Practical, "how to" chapters serve as training aids, and each section stands on its own as a concise, easy-to-access resource...
This text is devoted to pharmaceutical freeze-drying in all its forms and in all its technological variations. Whether you freeze-dry nonsterile table...
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cena:
803,99 zł |
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Good Drug Regulatory Practices : A Regulatory Affairs Quality Manual
ISBN: 9781574910513 / Angielski / Twarda / 440 str. Termin realizacji zamówienia: ok. 5-8 dni roboczych. Good Drug Regulatory Practices offers a series of policies and procedures to assure quality and timely regulatory submissions to national regulatory agencies. This book begins with introductory chapters describing the need for policy documentation, and the philosophy underlying the policies, and presents policies and standards that can be used as presented or adapted to individual situations in your company.
Good Drug Regulatory Practices offers a series of policies and procedures to assure quality and timely regulatory submissions to national regulatory a...
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cena:
933,66 zł |
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Quality and GMP Auditing: Clear and Simple
ISBN: 9781574910551 / Angielski / Twarda / 240 str. Termin realizacji zamówienia: ok. 5-8 dni roboczych. This guidebook provides proven methods and techniques for performing effective audits that serve your department, your company, and you. Topics covered relate to the four key competencies essential for successful GMP audits. Includes the rationale for auditing as an important quality tool, along with the audit cycle, broken into five distinct phases. To focus the power of auditing on a particular situation, several different types of audits are presented, as are more than a dozen audit approaches with general questions to answer and specific items to examine. These tools will help you prepare...
This guidebook provides proven methods and techniques for performing effective audits that serve your department, your company, and you. Topics covere...
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cena:
907,73 zł |
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Sterilization of Drugs and Devices : Technologies for the 21st Century
ISBN: 9781574910605 / Angielski / Twarda / 576 str. Termin realizacji zamówienia: ok. 5-8 dni roboczych. Editors Fred M. Nordhauser and Wayne P. Olson have gathered a team of 18 experts from multi-national and leading edge companies to explore the advantages and disadvantages of current sterilization technologies. They cover the theory behind the technology, the practical concerns of installation from engineering and product development perspectives, the "how to validate" concern, and the pragmatics of implementation in a manner that will satisfy the regulatory agencies. The broad range of in-depth information on numerous technologies will help readers design sterile manufacturing processes cost...
Editors Fred M. Nordhauser and Wayne P. Olson have gathered a team of 18 experts from multi-national and leading edge companies to explore the advanta...
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cena:
2074,80 zł |
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Control of Particulate Matter Contamination in Healthcare Manufacturing
ISBN: 9781574910728 / Angielski / Twarda / 574 str. Termin realizacji zamówienia: ok. 5-8 dni roboczych. Identify effective means of detection of particles Understand and interpret current environmental, GMP and other standards, and requirements for contamination control Learn the sources and characteristics of contaminant particles Set up requirements and test methods for injectable solutions and medical devices Conduct visual inspections, light extinction particle counting, airborne particle counting, and environmental monitoring Validate particle counting instrument systems Sample and collect particulate matter for analysis This book offers practical applications addressing the specifics of...
Identify effective means of detection of particles Understand and interpret current environmental, GMP and other standards, and requirements for conta...
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cena:
1945,13 zł |
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International Stability Testing
ISBN: 9781574910780 / Angielski / Twarda / 352 str. Termin realizacji zamówienia: ok. 5-8 dni roboczych. Provides the only single-volume reference for stability requirement in all major markets Discusses all aspects of stability testing, including ICH stability guidelines Supports the text with real-world examples 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. Participants in the ICH debates interpret the ICH guidelines. Other discussions focus on European requirements, the ICH initiatives, the US SUPAC...
Provides the only single-volume reference for stability requirement in all major markets Discusses all aspects of stability testing, including ICH sta...
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cena:
855,86 zł |
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Pharmaceutical Equipment Validation: The Ultimate Qualification Guidebook
ISBN: 9781574910797 / Angielski / Twarda / 456 str. Termin realizacji zamówienia: ok. 5-8 dni roboczych. While FDA regulations, cGMP, GLP, GCP, and the industry standard ISO 9000 require that documentation be established and followed, they do not provide guidelines on how to produce that documentation. Pharmaceutical Equipment Validation gives details on how to demonstrate compliance, what data to use, and how to produce the appropriate documentation. This book's user-friendly diagrams and other clear graphics illustrate key ideas throughout each protocol, offering a bird's-eye view of what is coming next-and they quickly guide you through the equipment validation. The author provides a thorough...
While FDA regulations, cGMP, GLP, GCP, and the industry standard ISO 9000 require that documentation be established and followed, they do not provide ...
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cena:
1089,27 zł |
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Lyophilization: Introduction and Basic Principles
ISBN: 9781574910810 / Angielski / Twarda / 664 str. Termin realizacji zamówienia: ok. 5-8 dni roboczych. Presenting information in an easy-to-read style, this book comprehensively and authoritatively covers lyophilization. Using plain, informative, unpretentious language, Jennings pulls together information from diverse sources to provide a basic introduction not only directed to lyophilizing solutions but also relevant to more complex systems containing rigid cellular structures. Including over 150 illustrations, global symbols, and more than 350 references, this book is the complete guide to lyophilization, its analytical methods, measurement of process parameters, and equipment. Generously...
Presenting information in an easy-to-read style, this book comprehensively and authoritatively covers lyophilization. Using plain, informative, unpret...
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cena:
1089,27 zł |
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Calibration in the Pharmaceutical Laboratory
ISBN: 9781574910926 / Angielski / Twarda / 336 str. Termin realizacji zamówienia: ok. 5-8 dni roboczych. Increasingly, pharmaceutical scientists must not only be specialists in their field but also must be familiar with legislation that governs the use of equipment in the industry. The regulation of test and measuring equipment changes continually as new regulations are introduced. Calibration in the Pharmaceutical Laboratory provides general background on laboratory balances and precision scales, insight into mass measurements and associated errors, and detailed information on key quality issues associated with weighing. Managers responsible for QC and QA should find this book a useful tool in...
Increasingly, pharmaceutical scientists must not only be specialists in their field but also must be familiar with legislation that governs the use of...
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cena:
596,51 zł |
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How to Develop and Manage Qualification Protocols for FDA Compliance
ISBN: 9781574910988 / Angielski / Twarda / 386 str. Termin realizacji zamówienia: ok. 5-8 dni roboczych. Explains in detail how to develop and manage qualification protocols and their associated documentation for all of the validation department functions Shows how to perform qualification testing and establish a requalification program Describes how various documents relate to each other and to an overall documentation system Discusses in details key function areas, such as Cleaning, Facilities and Utilities, Equipment, Computers and Software, and Process Provides ready-to-use protocols and protocol templates All current Good Manufacturing Practices (cGMP), Good Clinical Practices (GCP), Good...
Explains in detail how to develop and manage qualification protocols and their associated documentation for all of the validation department functions...
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cena:
248,92 zł |
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Cleaning Validation: A Practical Approach
ISBN: 9781574911084 / Angielski / Twarda / 200 str. Termin realizacji zamówienia: ok. 5-8 dni roboczych. Offering a detailed, step-by-step guide to building a compliant cleaning validation program, Cleaning Validation: A Practical Approach covers trends in control, procedures, cleaning agents and tools, sampling techniques, analytical methods, and regulatory issues. The author provides practical examples, database formats, standard operating procedures, work instructions, protocols, and reports. He gives readers the tools they need to develop an effective and manageable program that will not only be acceptable to both US and non-US regulatory authorities but will conserve an organization's time,...
Offering a detailed, step-by-step guide to building a compliant cleaning validation program, Cleaning Validation: A Practical Approach covers trends i...
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cena:
855,86 zł |
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