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Pragmatic Flutter Building Cross-Platform Mobile Apps for Android iOS Web & Desktop

Pragmatic Flutter Building Cross-Platform Mobile Apps for Android iOS Web & Desktop

Have you ever thought of creating beautiful blazing-fast native apps for iOS and Android from a single codebase? Have you dreamt of taking your native apps to the web and desktop without it costing a fortune? If so Pragmatic Flutter: Building Cross-Platform Mobile Apps for Android iOS Web & Desktop is the right place to start your journey to developing cross-platform apps. Google’s Flutter is the brand-new way for developing beautiful fluid and blazing-fast cross-platform apps for Android iOS web and desktops (macOS Linux Windows). Google’s new Fuchsia OS user interface (UI) is implemented using Flutter as well. Learning to develop mobile apps with Flutter opens the door to multiple devices form-factors and platforms using a single codebase. You don’t need any prior experience using Dart to follow along in this book; however it’s recommended that readers have some familiarity with writing code using one of the object-oriented programming languages. Your journey starts with learning to structure and organize the Flutter project to develop apps for multiple platforms. Next you will explore the fundamentals of Flutter widgets. The journey continues with Flutter’s layout widgets while also learning to build responsive layouts. You will get an understanding of organizing and applying themes and styles handling user input and gestures. Then you will move on to advanced concepts such as fetching data over the network and integrating and consuming REST API in your app. You will get hands-on experience on design patterns data modeling routing and navigation for multi-screen apps. When you are finished you will have a solid foundational knowledge of Flutter that will help you move on to building great and successful mobile apps that can be deployed to Android iOS web and desktop (macOS Linux Windows) platforms from a single codebase. | Pragmatic Flutter Building Cross-Platform Mobile Apps for Android iOS Web & Desktop

GBP 105.00
1

Introductory Semiconductor Device Physics

An In-Depth Guide to Mobile Device Forensics

Handbook of Medical Device Regulatory Affairs in Asia Second Edition

Quantum Mechanics An Introduction for Device Physicists and Electrical Engineers

Introductory Nanoelectronics Physical Theory and Device Analysis

Semiconductor Nanocrystals and Metal Nanoparticles Physical Properties and Device Applications

Semiconductor Nanocrystals and Metal Nanoparticles Physical Properties and Device Applications

Semiconductor nanocrystals and metal nanoparticles are the building blocks of the next generation of electronic optoelectronic and photonic devices. Covering this rapidly developing and interdisciplinary field the book examines in detail the physical properties and device applications of semiconductor nanocrystals and metal nanoparticles. It begins with a review of the synthesis and characterization of various semiconductor nanocrystals and metal nanoparticles and goes on to discuss in detail their optical light emission and electrical properties. It then illustrates some exciting applications of nanoelectronic devices (memristors and single-electron devices) and optoelectronic devices (UV detectors quantum dot lasers and solar cells) as well as other applications (gas sensors and metallic nanopastes for power electronics packaging). Focuses on a new class of materials that exhibit fascinating physical properties and have many exciting device applications. Presents an overview of synthesis strategies and characterization techniques for various semiconductor nanocrystal and metal nanoparticles. Examines in detail the optical/optoelectronic properties light emission properties and electrical properties of semiconductor nanocrystals and metal nanoparticles. Reviews applications in nanoelectronic devices optoelectronic devices and photonic devices. | Semiconductor Nanocrystals and Metal Nanoparticles Physical Properties and Device Applications

GBP 66.99
1

Mobile Point-of-Care Monitors and Diagnostic Device Design

Design Controls for the Medical Device Industry Third Edition

Design Controls for the Medical Device Industry Third Edition

This third edition provides a substantial comprehensive review of the latest design control requirements as well as proven tools and techniques to ensure a company's design control program evolves in accordance with current industry practice. It assists in the development of an effective design control program that not only satisfies the US FDA Quality Systems Regulation (QSR) and 13485:2016 standards but also meets today's Notified Body Auditors' and FDA Investigators' expectations. The book includes a review of the design control elements such as design planning input output review verification validation change transfer and history as well as risk management inclusive of human factors and usability biocompatibility the FDA Quality System Inspection Technique (QSIT) for design controls and medical device regulations and classes in the US Canada and Europe. Practical advice methods and appendixes are provided to assist with implementation of a compliant design control program and extensive references are provided for further study. This third edition: Examines new coverage of ISO 13485-2016 design control requirements Explores proven techniques and methods for compliance Contributes fresh templates for practical implementation Provides updated chapters with additional details for greater understanding and compliance Offers an easy to understand breakdown of design control requirements Reference to MDSAP design control requirements | Design Controls for the Medical Device Industry Third Edition

GBP 150.00
1

Validation Standard Operating Procedures A Step by Step Guide for Achieving Compliance in the Pharmaceutical Medical Device and Biotech

Handbook of Optoelectronic Device Modeling and Simulation Fundamentals Materials Nanostructures LEDs and Amplifiers Vol. 1

Bringing a Medical Device to the Market A Scientist’s Perspective

Handbook of Optoelectronic Device Modeling and Simulation Lasers Modulators Photodetectors Solar Cells and Numerical Methods Vol. 2

ISO 13485:2016 A Complete Guide to Quality Management in the Medical Device Industry Second Edition

ISO 13485:2016 A Complete Guide to Quality Management in the Medical Device Industry Second Edition

Summary: This book provides valuable effective guidance for understanding interpreting and implementing ISO 13485:2016 standard requirements. Despite its more than 800-page length the author has specifically designed its contents to maximize usability for the reader with a table of contents identical to that of the ISO standard itself which enables easy navigation and orientation. Pragmatic in style and down to earth in tone this book draws real-life examples and case-studies from the author’s many years of experience in consulting to illustrate even the most complex of ISO 13485:2016 standard requirements and their implementation. Identifying relevant requirements and how they harmonize with quality management systems developing processes for design and development as well as product realization and validation are just a few of the issues covered in-depth by this publication. In addition the author constantly reviews the distinctive characteristics and aspects of the medical device manufacturing industry so that the reader can also appreciate the subject of this book in an everyday context. Features: A pragmatic and down to earth approach towards the reader’s understanding of ISO 13485:2016 standard requirements implementation. Uses examples and cases from real-life based on the author’s many years of experience in quality management. A table of contents structured identically to that of ISO 13485:2016 itself allowing easier navigation and orientation for the reader. Emphasises guidance for ISO 13495:2016 standard requirements which are difficult to interpret and implement Constantly reviews the aspect of medical device industry characteristics and distinctive so the reader can reflect the content with its daily work. | ISO 13485:2016 A Complete Guide to Quality Management in the Medical Device Industry Second Edition

GBP 150.00
1

Pipeline Valve Technology A Practical Guide

Pipeline Valve Technology A Practical Guide

The e-book+ version of the book Pipeline Valve Technology complements the other versions of the book. The e-book+ version provides the user with additional questions and answers at the end of each chapter to gauge and enhance the user’s understanding. The book covers the life cycle of pipeline valves the largest and most essential valves in offshore pipeline engineering. Discussing the design process testing production transportation installation and maintenance the book also covers the risk analysis required to assess the reliability of these valves. Pipeline valves require particular attention to ensure they are safely designed installed and maintained due to the high stakes. Failure would result in environmental pollution the destruction of expensive assets and potential loss of life. Proper installation and upkeep require specialist processes throughout the life cycle of the valve. This book is a key guide to these processes. Beginning by looking at the design of pipeline valves this book details how conserving weight and space is prioritized how materials are chosen how thickness is calculated and how leakage is minimized. It then discusses production and specific welding techniques to bond dissimilar materials alongside casting and machining. Building on other discussions in the text with case studies and questions and answers for self-study this book is the ideal guide to pipeline valves. This book will be of interest to professionals in the industries of offshore oil and gas material engineering coatings mechanical engineering and piping. It will also be relevant to students studying coating and welding or mechanical piping or petroleum engineering. | Pipeline Valve Technology A Practical Guide

GBP 68.99
1

Developing an ISO 13485-Certified Quality Management System An Implementation Guide for the Medical-Device Industry

Developing an ISO 13485-Certified Quality Management System An Implementation Guide for the Medical-Device Industry

Developing an ISO 13485-Certified Quality Management System: An Implementation Guide for the Medical-Device Industry details the lessons learned from a real-world project focusing on building an ISO 13485:2016 Quality Management System (QMS) from scratch and then having it officially certified. It is a practical guide to building or improving your existing QMS with tried and tested solutions. The book takes a hands-on approach–first teaching the top 25 lessons to know before starting to develop a QMS and then walking you through the process of writing the quality manual and the standard operating procedures training the staff on the QMS organizing an internal audit executing a management review and finally passing the necessary external audits and obtaining certification. It helps you to progress from one task to the next and provides all the essential information to accomplish each task as quickly and efficiently as possible. It does not attempt to replicate the standard but instead drills into the standard to expose the core of each section of the standard and reorganize its contents into a practical workflow for developing maintaining and improving a Lean QMS. The book includes a wealth of real-world experience both from the author's personal dive into quality management and from the experiences of other companies in the field and provides handy checklists for ensuring key documents and processes are fit for use–the emphasis here is to help ensure you have considered all relevant aspects. In addition the book is not intended as a “cheat sheet” for the standard or as a review of the standard that only adds lengthy commentary on each of the clauses. Instead the book fixes easy misunderstandings regarding QMS provides insight into why the various clauses are written the way they are and provides a great base to both understanding ISO 13485 QMS and developing your own QMS. The book is intended to serve both experts and novices audiences–it provides special insight on the most crucial and effective aspects of QMS. | Developing an ISO 13485-Certified Quality Management System An Implementation Guide for the Medical-Device Industry

GBP 48.99
1

FinFET Devices for VLSI Circuits and Systems

Medical-Grade Software Development How to Build Medical-Device Products That Meet the Requirements of IEC 62304 and ISO 13485

Medical-Grade Software Development How to Build Medical-Device Products That Meet the Requirements of IEC 62304 and ISO 13485

This book is a practical guide to meeting IEC 62304 software-development requirements within the context of an ISO 13485 quality management system (QMS). The book proves this can be done with a minimum amount of friction overlap and back-and-forth between development stages. It essentially shows you how you should shape your medical-software development processes to fit in with the QMS processes in the smartest and leanest way possible. By following the advice in this book you can reuse processes from your QMS ensure your product-realization processes meet the requirements for medical-software development and marry all the requirements together using tried and tested solutions into one efficient system. The expertise of the authors here goes beyond just the experiences of one real-world project as they tap into over 30 years of experience and countless software and software-assessment projects to distill their advice. The book takes a hands-on approach by first teaching you the top 25 lessons to know before starting to develop a process for medical-software development. It then walks you through the expectations placed on the key aspects of such a process by the key standards. The book progresses from an overview of both standards and the general requirements involved to a detailed discussion of the expected stages from software development and maintenance to risk management configuration management and problem resolution. The book provides insightful advice on how the requirements of the IEC 62304 software-development life cycle can be married with an ISO 13485 QMS how the development of the technical file should be organized and how to address conformity assessment the daily after-approval and the recent trends that will affect the industry in the coming years. The book is modeled after the IEC 62304 standard and adopts its clause structure in the numbering of sections for easy reference. The book does not attempt to replicate either standard. For the ISO 13485 standard it recites the necessary requirements succinctly. For IEC 62304 the discussion is in-depth and also addresses the impact of ISO 13485 on the requirements discussed. In this way the book drills into both standards to expose the core of each requirement and shape these into a practical cohesive workflow for developing maintaining and improving a Lean software development pipeline. | Medical-Grade Software Development How to Build Medical-Device Products That Meet the Requirements of IEC 62304 and ISO 13485

GBP 45.99
1

Silicon Based Unified Memory Devices and Technology

Medical Devices A Practical Guide

Medical Regulatory Affairs An International Handbook for Medical Devices and Healthcare Products

Gallium Nitride Power Devices