The 'Blue Guide' on the Implementation of EU Product Rules

The 'Blue Guide' on the Implementation of EU Product Rules

Author:

Publisher:

Published: 2015

Total Pages: 133

ISBN-13: 9789279359989

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The Guide to the implementation of directives based on the New Approach and the Global Approach (the "Blue Guide") was published in 2000. Since then, it has become one of the main reference documents explaining how to implement the legislation based on the New Approach, now covered by the New Legislative Framework. Much of the 2000 edition of the "Blue Guide" is still valid but it requires updating to cover new developments and to ensure the broadest possible common understanding on implementation of the New Legislative Framework (NLF) for the marketing of products. It is also necessary to take account of the changes introduced by the Lisbon Treaty (in force since 1st December 2009) with regard to the legal references and terminology applicable to EU-related documents, procedures, etc. This new version of the Guide will therefore build on the past edition, but include new chapters, for example on the obligations of economic operators or accreditation, or completely revised chapters such as those on standardisation or market surveillance. The Guide has also been given a new title reflecting the fact that the New Legislative Framework is likely to be used, at least in part, by all types of Union harmonisation legislation and not only by the so-called "New Approach" directives.


Specialized Administrative Law of the European Union

Specialized Administrative Law of the European Union

Author: Herwig C. H. Hofmann

Publisher: Oxford University Press

Published: 2018-11-30

Total Pages: 892

ISBN-13: 0191091294

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This volume deals with the law governing the administrative implementation of European Union public policy. Much of this law is specific to individual policy sectors. The volume provides a study of such specialized admininstrative law for more than twenty sectors. This cross-sectoral approach allows for detailed comparisons of EU administration in diverse policy fields. It identifies situations where legal structures and approaches may be unnecessarily duplicated, thus indicating where a comprehensive, general system could be advantageous for both Union law and policy achievement. The comparative nature of the study also draws attention to policy fields which have proven to be testing grounds for approaches adopted subsequently in other areas. In addition, the work highlights the distinctive, highly networked, and strongly cooperative character of EU administration, as a reflection of, and a foundation for, the operative nature of the European Union as a whole.


Handbook of Surgical Planning and 3D Printing

Handbook of Surgical Planning and 3D Printing

Author: Paolo Gargiulo

Publisher: Elsevier

Published: 2023-03-23

Total Pages: 467

ISBN-13: 0323910408

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Handbook of Surgical Planning and 3D Printing: Applications, Integration, and New Directions?covers 3D printing and surgical planning from clinical, technical and economic points-of-view. This book fills knowledge gaps by addressing: (1) What type of medical images are needed for 3D printing, and for which specific application? (2) What software should be used to process the images, should the software be considered a medical device? (3) Data protection? (4) What are the possible clinical applications and differences in imaging, segmentation, and 3D printing? And finally, (5) What skills, resources, and organization are needed? Sections cover technologies involved in 3D printing in health: data structure, medical images and segmentation, printing materials and 3d printing, 3D printing and Clinical Applications: orthopedic surgery, neurosurgery, maxillofacial, orthodontistry, surgical guides, integrating 3D printing Service in Hospitals: infrastructures, competences, organization and cost/benefits, and more. Provides a unique insight into a technological process and its applications Heps readers find answers to practical and technical questions concerning 3D printing and surgical planning Presents deep insights into new directions of 3D printing in healthcare and related emerging applications such as bioprinting, biocompatible materials and metal printing for custom-made prosthetic design


The Law and Policy of New Eurasian Regionalization

The Law and Policy of New Eurasian Regionalization

Author: Anna Aseeva

Publisher: BRILL

Published: 2021-01-25

Total Pages: 678

ISBN-13: 9004447873

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Drawing on international, transnational, and comparative legal scholarship, The Law and Policy of New Eurasian Regionalization: Economic Integration, Trade, and Investment in the Post-Soviet and Greater Eurasian Space, additionally offers the insights of a plethora of leading international scholars in economics, institutional theory, area studies, international relations, global political economy, political science, and sociology. The contributors come from four corners of the globe, including Asia, Europe, and North America.


Third-Party Certifiers

Third-Party Certifiers

Author: Jan De Bruyne

Publisher: Kluwer Law International B.V.

Published: 2019-07-12

Total Pages: 691

ISBN-13: 9403510927

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Third-Party Certifiers Jan De Bruyne Third-party certifiers are organisations that are independent a requesting entity. They attest that a product, service, information or person possesses certain qualifications or meets safety, quality or technical standards. This important book presents an in-depth analysis of the liability and obligations of certifiers, evaluates existing certification processes in selected fields and proposes new mechanisms which could increase the accuracy and reliability of certifiers’ ratings, marks or reports. Highlighting the risks of errors in this activity – inaccurate certification was a major factor in the global financial crisis of 2008 – the author takes a comparative approach, looking at the certification process in several European countries, Australia and the United States. Such aspects of the process as the following are thoroughly described: obligations and liability of certifiers during the certification process; risk of ‘information asymmetry’ between the requesting entity and the end user; and relationship between the civil liability of certifiers and public law aspects. The analysis includes detailed research on key industries and jurisdictions and a specific proposed framework for more accurate and reliable certification. Because the efficient and effective functioning of third-party certifiers is extremely important in today’s world – especially in such areas as health, the environment, safety or economic values – this deeply researched contribution to an important area of commercial law, combining analysis of current issues with proposed reforms, will be welcomed by practitioners when confronted with legal issues with regard to the certification process. The book’s conceptual framework will also prove highly useful for policymakers charged with developing reliable certification mechanisms.


UK, EU and Global Administrative Law

UK, EU and Global Administrative Law

Author: Paul Craig

Publisher: Cambridge University Press

Published: 2015-10-26

Total Pages: 845

ISBN-13: 110712512X

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A detailed analysis of the foundations and challenges of UK, EU and global administrative law.


Research Handbook on the Enforcement of EU Law

Research Handbook on the Enforcement of EU Law

Author: Miroslava Scholten

Publisher: Edward Elgar Publishing

Published: 2023-09-06

Total Pages: 581

ISBN-13: 1802208038

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This comprehensive Research Handbook investigates the success of EU law enforcement processes. Going beyond traditional analyses of administrations and courts in isolation, it focuses on the increased cooperation seen between national and EU authorities, and on the widening variety of means used to enhance compliance with EU norms.


New Frontiers for Design of Interior Lighting Products

New Frontiers for Design of Interior Lighting Products

Author: Andrea Siniscalco

Publisher: Springer Nature

Published: 2021-05-27

Total Pages: 128

ISBN-13: 303075782X

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This book explores the single components that commonly constitute luminaires for interiors, describing their operating principles, families, strengths and weaknesses. It opens with the product classification and main standard requirements. The following chapters describe the different components: light sources, power supplies, thermal dissipation techniques, control technologies, optical systems. The description focuses on the most recent technologies to allow the reader to consider a product design capable of confronting future lighting scenarios. The book provides a simple path addressed to all those who want to try their hand at designing luminaires for interiors, even without a specific engineering background.


Managing Medical Devices within a Regulatory Framework

Managing Medical Devices within a Regulatory Framework

Author: Beth Ann Fiedler

Publisher: Elsevier

Published: 2016-09-10

Total Pages: 382

ISBN-13: 0128041927

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Managing Medical Devices within a Regulatory Framework helps administrators, designers, manufacturers, clinical engineers, and biomedical support staff to navigate worldwide regulation, carefully consider the parameters for medical equipment patient safety, anticipate problems with equipment, and efficiently manage medical device acquisition budgets throughout the total product life cycle. This contributed book contains perspectives from industry professionals and academics providing a comprehensive look at health technology management (HTM) best practices for medical records management, interoperability between and among devices outside of healthcare, and the dynamics of implementation of new devices. Various chapters advise on how to achieve patient confidentiality compliance for medical devices and their software, discuss legal issues surrounding device use in the hospital environment of care, the impact of device failures on patient safety, methods to advance skillsets for HTM professionals, and resources to assess digital technology. The authors bring forth relevant challenges and demonstrate how management can foster increased clinical and non-clinical collaboration to enhance patient outcomes and the bottom line by translating the regulatory impact on operational requirements. Covers compliance with FDA and CE regulations, plus EU directives for service and maintenance of medical devices Provides operational and clinical practice recommendations in regard to regulatory changes for risk management Discusses best practices for equipment procurement and maintenance Provides guidance on dealing with the challenge of medical records management and compliance with patient confidentiality using information from medical devices