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Author : Jeffrey Gibbs
Publisher :
ISBN 13 : 9781935065890
Total Pages : pages
Book Rating : 4.90/5 ( download)
Download or read book Diagnostics at a Crossroads: Navigating IVD Regulation in a Changing Environment written by Jeffrey Gibbs and published by . This book was released on 2020-12-20 with total page pages. Available in PDF, EPUB and Kindle. Book excerpt:
Author : Gloria Hall
Publisher :
ISBN 13 : 9781947493674
Total Pages : pages
Book Rating : 4.71/5 ( download)
Download or read book Fundamentals of Medical Device Regulations, Fourth Edition written by Gloria Hall and published by . This book was released on 2021-07-23 with total page pages. Available in PDF, EPUB and Kindle. Book excerpt:
Author : Wolfgang Ecker
Publisher : BoD – Books on Demand
ISBN 13 : 3754384848
Total Pages : 346 pages
Book Rating : 4.48/5 ( download)
Download or read book Medical Devices and IVDs written by Wolfgang Ecker and published by BoD – Books on Demand. This book was released on 2022-03-25 with total page 346 pages. Available in PDF, EPUB and Kindle. Book excerpt: With this book, you get a really complete seminar for the new Regulations on medical devices and IVDs in the EU, ready at hand, at any time. These EU regulations create new rules for medical technology and laboratory diagnostics in Europe. Concise regulatory know-how is now required to keep or reposition medical devices and in vitro diagnostics on the European market, from syringes, contact lenses, medical device apps, pregnancy tests, nuclear magnetic resonance tomography to cancer tests, genetic diagnostics, HIV tests, hip implants, heart catheters, artificial spinal discs, stents and pacemakers. Concise regulatory training and further education of employees in companies and health care facilities is the order of the day. This also applies to biomedical and medical technology students at universities of applied sciences and biomedical universities, start-ups and spin-offs, who must make use of this know-how from the initial product idea through the further stages of product development to market access. The book provides a thorough, compact course on the new regulations, starting with perfect overview and easy navigation and going into depth where you need it: this book will make you fit and confident for the new European challenges!
Author : World Health Organization
Publisher :
ISBN 13 : 9789241512350
Total Pages : 72 pages
Book Rating : 4.50/5 ( download)
Download or read book WHO Global Model Regulatory Framework for Medical Devices Including in Vitro Diagnostic Medical Devices written by World Health Organization and published by . This book was released on 2017-05-09 with total page 72 pages. Available in PDF, EPUB and Kindle. Book excerpt: The Model recommends guiding principles and harmonized definitions and specifies the attributes of effective and efficient regulation to be embodied within binding and enforceable law. Its main elements refer to international harmonization guidance documents developed by the Global Harmonization Task Force (GHTF) and its successor, the International Medical Device Regulators Forum (IMDRF). The Model is particularly relevant for WHO Member States with little or no regulation for medical devices currently in place but with the ambition to improve this situation. It foresees that such countries will progress from basic regulatory controls towards an expanded level to the extent that their resources allow. The Model is written for the legislative, executive, and regulatory branches of government as they develop and establish a system of medical devices regulation. It describes the role and responsibilities of a country's regulatory authority for implementing and enforcing the regulations. Also, it describes circumstances in which a regulatory authority may either "rely on" or "recognize" the work products from trusted regulatory sources (such as scientific assessments, audit, and inspection reports) or from the WHO Prequalification Team. Section 2 of this document recommends definitions of the terms "medical devices" and IVDs. It describes how they may be grouped according to their potential for harm to the patient or user and specifies principles of safety and performance that the device manufacturer must adhere to. It explains how the manufacturer must demonstrate to a regulatory authority that its medical device has been designed and manufactured to be safe and to perform as intended during its lifetime. Section 3 presents the principles of good regulatory practice and enabling conditions for effectively regulating medical devices. It then introduces essential tools for regulation, explaining the function of the regulatory entity and the resources required. Section 4 presents a stepwise approach to implementing and enforcing regulatory controls for medical devices as the regulation progresses from a basic to an expanded level. It describes elements from which a country may choose according to national priorities and challenges. Also, it provides information on when the techniques of reliance and recognition may be considered and on the importance of international convergence of regulatory practice.Section 5 provides a list of additional topics to be considered when developing and implementing regulations for medical devices. It explains the relevance of these topics and provides guidance for regulatory authorities to ensure that they are addressed appropriately. The Model outlines a general approach but cannot provide country-specific guidance on implementation. While it does not offer detailed guidance on regulatory topics, it contains references to relevant documents where further information may be found. It does not detail the responsibilities of other stakeholders such as manufacturers, distributors, procurement agencies, and health-care professionals, all of whom have roles in assuring the quality, safety, and performance of medical devices.
Author : Gloria Hall
Publisher :
ISBN 13 : 9781947493612
Total Pages : pages
Book Rating : 4.12/5 ( download)
Download or read book Software As a Medical Device written by Gloria Hall and published by . This book was released on 2021-04-23 with total page pages. Available in PDF, EPUB and Kindle. Book excerpt:
Author : Keith Summerhayes
Publisher : Inst of Clinical Research
ISBN 13 : 0954934555
Total Pages : 94 pages
Book Rating : 4.52/5 ( download)
Download or read book The Challenges of Conducting Medical Device Studies written by Keith Summerhayes and published by Inst of Clinical Research. This book was released on 2005 with total page 94 pages. Available in PDF, EPUB and Kindle. Book excerpt: Describing all the regulations, guidelines and directives that affect medical device studies.
Author : Gloria Hall
Publisher :
ISBN 13 : 9781947493490
Total Pages : 726 pages
Book Rating : 4.93/5 ( download)
Download or read book Fundamentals of Medical Device Regulations, Third Edition written by Gloria Hall and published by . This book was released on 2020-07-29 with total page 726 pages. Available in PDF, EPUB and Kindle. Book excerpt: Fundamentals of Medical Device Regulations is a compilation of history, medical device and in vitro diagnotic (IVD) medical device information from RAPS' regional publications: Fundamentals of US Regulatory Affairs, Eleventh Edition; Fundamentals of Canadian Medical Device Regulations; Fundamentals of EU Regulatory Affairs, Ninth Edition; Fundamentals of International Regulatory Affairs, Fourth Edition."--Foreword.
Author :
Publisher :
ISBN 13 :
Total Pages : 48 pages
Book Rating : 4.71/5 ( download)
Download or read book Guideline for the Manufacture of in Vitro Diagnostic Products written by and published by . This book was released on 1990 with total page 48 pages. Available in PDF, EPUB and Kindle. Book excerpt:
Author : Val Theisz
Publisher : CRC Press
ISBN 13 : 9814669113
Total Pages : 578 pages
Book Rating : 4.15/5 ( download)
Download or read book Medical Device Regulatory Practices written by Val Theisz and published by CRC Press. This book was released on 2015-08-03 with total page 578 pages. Available in PDF, EPUB and Kindle. Book excerpt: This book is intended to serve as a reference for professionals in the medical device industry, particularly those seeking to learn from practical examples and case studies. Medical devices, like pharmaceuticals, are highly regulated, and the bar is raised constantly as patients and consumers expect the best-quality healthcare and safe and effectiv
Author : WHO Regional Office for South-East Asia
Publisher :
ISBN 13 : 9789290223962
Total Pages : 0 pages
Book Rating : 4.60/5 ( download)
Download or read book Development of National Health Laboratory Policy and Plan written by WHO Regional Office for South-East Asia and published by . This book was released on 2011 with total page 0 pages. Available in PDF, EPUB and Kindle. Book excerpt: This document provides technical support to Member States in the South-East Asia and Western Pacific Regions on the steps required to develop and effectively implement a national laboratory policy and national laboratory plan in accordance with the Asia Pacific Strategy for Strengthening Health Laboratory Services (2010-2015). The document provides a structure for developing a comprehensive policy and regulatory framework for establishing, operating and monitoring the health laboratory services, and promoting better coordination of activities among health programs and institutions for efficient support to both clinical and public health services.
