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Food Allergy Molecular and Clinical Practice

Textbook of Allergy for the Clinician

Monographs in Contact Allergy Volume 1 Non-Fragrance Allergens in Cosmetics (Part 1 and Part 2)

Monographs in Contact Allergy Volume 1 Non-Fragrance Allergens in Cosmetics (Part 1 and Part 2)

Monographs in Contact Allergy Volume 1: Non-Fragrance Allergens in Cosmetics (Part 1 and Part 2) is the first 2-part volume in an exciting series on contact allergy. It presents over 500 natural or synthetic chemicals and compounds which have caused allergic contact dermatitis in cosmetic products. Included here are INCI names synonyms description/definition CAS and EU numbers chemical class function in cosmetics molecular formula structural formula and advice on patch tests. A full literature review is given of patch testing in patients case reports of cosmetic allergic contact dermatitis irritant contact dermatitis photosensitivity immediate contact reactions and systemic side effects. This text is suitable for anyone with an interest in contact allergy from university students to professionals and all readers will find this informative and detailed series an invaluable resource. Key Features: Monographs of all known non-fragrance chemicals and substances which have caused allergic contact dermatitis from their presence in cosmetic products Provides lists of all functional groups (such as antioxidants preservatives artificial nail building emollients hair dyeing hair colorants) in both the EU and US formats and all chemicals in these groups which have caused cosmetic allergy Presents an alphabetical list of all synonyms indicating their INCI names Reported cross-reactions pseudo-cross-reactions and co-reactions patch test sensitization and presence in cosmetic products (including data from FDA’s Voluntary Cosmetic Registration Program) and chemical analyses are discussed Covers an extensive amount of information to benefit dermatologists allergists and non-medical professionals involved with the research development and marketing of cosmetic products | Monographs in Contact Allergy Volume 1 Non-Fragrance Allergens in Cosmetics (Part 1 and Part 2)

GBP 66.99
1

Nail Disorders A Comprehensive Approach

Forensic Anthropology A Comprehensive Introduction Second Edition

A Comprehensive Study of SQL Practice and Implementation

Quality Control Training Manual Comprehensive Training Guide for API Finished Pharmaceutical and Biotechnologies Laboratories

Quality Control Training Manual Comprehensive Training Guide for API Finished Pharmaceutical and Biotechnologies Laboratories

Written to help companies comply with GMP GLP and validation requirements imposed by the FDA and regulatory bodies worldwide Quality Control Training Manual: Comprehensive Training Guide for API Finished Pharmaceutical and Biotechnologies Laboratories presents cost-effective training courses that cover how to apply advances in the life sciences to produce commercially viable biotech products and services in terms of quality safety and efficacy. This book and its accompanying downloadable resources comprise detailed text summaries test papers and answers to test papers providing an administrative solution for management. Provides the FDA Health Canada WHO and EMEA guidelines directly applicable to pharmaceutical laboratory-related issuesOffers generic formats and styles that can be customized to any organization and help management build quality into routine operations to comply with regulatory requirementsContains ready-to-use training courses that supply a good source of training material for experienced and inexperienced practitioners in the biotechnology/biopharmaceutical industriesIncludes downloadable resources with downloadable training courses that can be adopted and directly customized to a particular organizationSupplies ready-to-use test papers that allow end users to record all raw data up to the issuance of the attached certificateThe biotechnology/bioscience industries are regulated worldwide to be in compliance with cGMP and GLP principles with particular focus on safety issues. Each company must create a definite training matrix of its employees. The training procedures in this book enable end users to understand the principles and elements of manufacturing techniques and provide documentation language ranging from the generic to the specific. The training courses on the downloadable resources supply valuable tools for developing training matrices to achieve FDA Health Canada EMEA MHRA UK WHO and GLP compliance. | Quality Control Training Manual Comprehensive Training Guide for API Finished Pharmaceutical and Biotechnologies Laboratories

GBP 52.99
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Oceanic Acidification A Comprehensive Overview

Rotating Machinery Research and Development Test Rigs

Cybercrime Investigations A Comprehensive Resource for Everyone

Cybercrime Investigations A Comprehensive Resource for Everyone

Cybercrime continues to skyrocket but we are not combatting it effectively yet. We need more cybercrime investigators from all backgrounds and working in every sector to conduct effective investigations. This book is a comprehensive resource for everyone who encounters and investigates cybercrime no matter their title including those working on behalf of law enforcement private organizations regulatory agencies or individual victims. It provides helpful background material about cybercrime's technological and legal underpinnings plus in-depth detail about the legal and practical aspects of conducting cybercrime investigations. Key features of this book include:Understanding cybercrime computers forensics and cybersecurityLaw for the cybercrime investigator including cybercrime offenses; cyber evidence-gathering; criminal private and regulatory law and nation-state implicationsCybercrime investigation from three key perspectives: law enforcement private sector and regulatoryFinancial investigationIdentification (attribution) of cyber-conductApprehensionLitigation in the criminal and civil arenas. This far-reaching book is an essential reference for prosecutors and law enforcement officers agents and analysts; as well as for private sector lawyers consultants information security professionals digital forensic examiners and more. It also functions as an excellent course book for educators and trainers. We need more investigators who know how to fight cybercrime and this book was written to achieve that goal. Authored by two former cybercrime prosecutors with a diverse array of expertise in criminal justice and the private sector this book is informative practical and readable with innovative methods and fascinating anecdotes throughout. | Cybercrime Investigations A Comprehensive Resource for Everyone

GBP 44.99
1

PgMP Exam Practice Test and Study Guide

PgMP Exam Practice Test and Study Guide

PgMP Exam Practice Test and Study Guide Fourth Edition is the book you need to pass the Program Management Professional (PgMP) exam the first time around. It reflects recent revisions based on PMI's Standard for Program Management - Third Edition (2013). Based on best practices that complement PMI‘s standards this is the most comprehensive and up-to-date resource available to help you prepare for the exam with new and changed terminology. It includes a list of the major topics covered on the exam organized by the five performance domains‘strategic program management program life cycle benefits management stakeholder management and governance as presented in the Program Management Professional Examination Content Outline. It also includes helpful tips on how to make the most of the time you have available to prepare for the exam. Just like its bestselling predecessors this indispensable study guide includes 20 multiple-choice practice questions for each domain along with a comprehensive answer key. The program life cycle domain includes 20 questions for each of the five phases. Each question also has a plainly written rationale for each correct answer with bibliographic references for further study. Two challenging 170-question practice tests that simulate the actual exam are included in the book and online so you can retake them as many times as necessary. They also include a rationale and reference. Scores for the online tests are presented as if each question is rated similarly but this edition also includes a new component: the authors own weighting system for the level of difficulty for each question. This system will show you what they feel meets the exam‘s criteria for Proficient Moderately Proficient and below Proficient. You then will see your scores by domain in both approaches. Supplying an in | PgMP® Exam Practice Test and Study Guide

GBP 175.00
1

The Duke Elder Exam of Ophthalmology A Comprehensive Guide for Success

Rare Lung Diseases A Comprehensive Clinical Guide to Diagnosis and Management

Military Medicine in Iraq and Afghanistan A Comprehensive Review

A Comprehensive Guide to Safety and Aging Minimizing Risk Maximizing Security

Complementary and Alternative Medicines in Prostate Cancer A Comprehensive Approach

Test Quality for Construction Materials and Structures Proceedings of the International RILEM/ILAC Symposium

Cleaning Validation Manual A Comprehensive Guide for the Pharmaceutical and Biotechnology Industries

Cleaning Validation Manual A Comprehensive Guide for the Pharmaceutical and Biotechnology Industries

During the past decades enormous progress and enhancement of pharmaceutical manufacturing equipment and its use have been made. And while there are support documents books articles and online resources available on the principles of cleaning and associated processing techniques none of them provides a single database with convenient ready-to-use training tools. Until now. Cleaning Validation Manual: A Comprehensive Guide for the Pharmaceutical and Biotechnology Industries elucidates how to train the man power involved in development manufacturing auditing and validation of bio pharmaceuticals on a pilot scale leading to scale-up production. With over 20 easy-to-use template protocols for cleaning validation of extensively used equipments this book provides technical solutions to assist in fulfilling the training needs of finished pharmaceutical manufacturers. Drawing on the authors’ more than two decades of experience in the pharmaceutical and biotech industries the text offers hands-on training based on current approaches and techniques. The book does not merely provide guidelines or thought processes rather it gives ready-to-use formulas to develop Master Plan SOPs and validation protocols. It includes cleaning procedures for the most commonly used equipment in various manufacturing areas and their sampling points using a pharmaceutical manufacturing site with both sterile and non-sterile operations as the case facility. It also provides the training guidelines on downloadable resources to enable users to amend or adopt them as necessary. Grounded in practicality the book’s applicability and accessibility set it apart. It can be used as a guide for implementing a cleaning validation program on site without the help of external consultants making it a resource that will not be found collecting dust on a shelf but rather referred to again and again. | Cleaning Validation Manual A Comprehensive Guide for the Pharmaceutical and Biotechnology Industries

GBP 105.00
1

Thermitic Thermodynamics A Computational Survey and Comprehensive Interpretation of Over 800 Combinations of Metals Metalloids and Oxides

GBP 170.00
1

The Privacy Leader Compass A Comprehensive Business-Oriented Roadmap for Building and Leading Practical Privacy Programs

The Privacy Leader Compass A Comprehensive Business-Oriented Roadmap for Building and Leading Practical Privacy Programs

476 Pages 57 B/W Illustrations Congratulations! Perhaps you have been appointed as the Chief Privacy Officer (CPO) or the Data Protection Officer (DPO) for your company. Or maybe you are an experienced CPO/DPO and you wonder – what can I learn from other successful privacy experts to be even more effective? Or perhaps you are considering a move from a different career path and deciding if this is the right direction for you. Seasoned award-winning Privacy and Cybersecurity leaders Dr. Valerie Lyons (Dublin Ireland) and Todd Fitzgerald (Chicago IL USA) have teamed up with over 60 award-winning CPOs DPOs highly respected privacy/data protection leaders data protection authorities and privacy standard setters who have fought the tough battle. Just as the #1 best-selling and CANON Cybersecurity Hall of Fame winning CISO Compass: Navigating Cybersecurity Leadership Challenges with Insights from Pioneers book provided actionable advice to Chief Information Security Officers The Privacy Leader Compass is about straight talk – delivering a comprehensive privacy roadmap applied to and organized by a time-tested organizational effectiveness model (the McKinsey 7-S Framework) with practical insightful stories and lessons learned. You own your continued success as a privacy leader. If you want a roadmap to build lead and sustain a program respected and supported by your board management organization and peers this book is for you. | The Privacy Leader Compass A Comprehensive Business-Oriented Roadmap for Building and Leading Practical Privacy Programs

GBP 44.99
1

Engineered Concrete Mix Design and Test Methods Second Edition

Engineered Concrete Mix Design and Test Methods Second Edition

As every civil engineer knows Portland Cement is the most versatile and important material of construction and will probably remain so far into the future. Yet few books if any exist that offer an in-depth analysis of the mixing and testing methods of this vital hydraulic cement. This statement written about the first edition of Engineered Concrete: Mix Design and Test Methods remains as true today as it was ten years ago. Revised and updated the second edition of this groundbreaking resource completely covers Portland Cement Portland Cement Concrete and their uses. See what‘s new in the Second Edition: New coverage of the latest concrete technologies such as high-performance and lightweight concrete Several new tests and sample tearsheets Additional and updated data sheets The body of the book is divided into several sections with the first explaining how concrete batches are designed mixed and measured for various consistencies. Another section details the tests of the primary component materials of concrete other than water namely Portland Cement aggregates and mortar while the final section includes some of the fundamental concrete testing procedures for different strength parameters in conformity with the standards of the American Society for Testing Materials. Solidly researched and written the book supplies a fundamental understanding of cement concrete and mixing and testing methods that allow readers to produce the most economical combinations of concrete materials and satisfy performance requirements and specifications. | Engineered Concrete Mix Design and Test Methods Second Edition

GBP 180.00
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Pharmaceutical Vendors Approval Manual A Comprehensive Quality Manual for API and Packaging Material Approval

Pharmaceutical Vendors Approval Manual A Comprehensive Quality Manual for API and Packaging Material Approval

This book provides stepwise guidance on how to evaluate audit qualify and approve an active pharmaceutical ingredient (API) and packaging material manufacturer and supplier to enhance the GMP within the industry. The book will also be beneficial for institutions conducting pharmaceutical technology courses in terms of GMP and GLP applications. The Pharmaceutical Vendors Approval Manual provides readers and front-line health care products manufacturers R&D management and biotech laboratories all the information they need to know to develop a GMP-oriented industry with trained and skilled personnel and manufacture products that meet GMP and regulatory requirements. This book provides a simple concise and easy to use reference tool covering basic quality concepts and the elements of vendor’s assessment qualification and approval required by the pharmaceutical educational institutions and professional certification bodies. It is equally relevant to Quality Assurance officers Quality Control Analysts Quality Auditors and other personnel involved in GMP/GLP services in the company. The book will also be beneficial for the institutions conducting Pharmaceutical technology study courses in terms of GMP and GLP applications. This book provides readers and front-line health care products manufacturers R&D management and biotech laboratories all the information they need to know to develop a GMP-oriented industry with trained and skilled personnel and manufacture products that meet GMP and regulatory requirements covers basic quality concepts and the elements of vendor’s assessment qualification and approval required by the pharmaceutical educational institutions and professional certification bodies provides stepwise guidance on how to evaluate audit qualify and approve an API and packaging material manufacturer and supplier to enhance the GMP within the industry provides ready to use regulatory documentation e. g. letter of commitment questionnaire SOP etc. required for API and Packaging Materials contract Provided material can be easily tailored to incorporate changes to add in-house vendor’s qualification requirements. Erfan Syed Asif Ph. D is a Senior Consultant at PharmEng Technology. | Pharmaceutical Vendors Approval Manual A Comprehensive Quality Manual for API and Packaging Material Approval

GBP 82.99
1

Clinical Oncology Basic Principles and Practice