CE Conformity Marking: and New Approach Directives
Autor Ray Trickeren Limba Engleză Paperback – 30 apr 2000
The prime aim of the CE Directive is to ensure that "all industrial products that are placed on the market do not compromise the safety and health of users when properly installed, maintained and used in accordance with their intended purpose. Users and third parties should be provided with a high level of protection and the devices should attain the performance levels claimed by the manufacturer."
This book explains the meaning of CE Marking, its history, how the Directive can affect all manufacturers of industrial products, its current status, its associated quality management requirements, and how manufacturers can easily and cost-effectively meet the requirements for CE Conformance.
- Essential information for any manufacturer or distributor wishing to trade in the European Union
- Practical and easy to understand
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Specificații
ISBN-13: 9780750648134
ISBN-10: 0750648139
Pagini: 285
Ilustrații: Approx. 100 illustrations
Dimensiuni: 156 x 234 x 17 mm
Greutate: 0.41 kg
Editura: ELSEVIER SCIENCE
ISBN-10: 0750648139
Pagini: 285
Ilustrații: Approx. 100 illustrations
Dimensiuni: 156 x 234 x 17 mm
Greutate: 0.41 kg
Editura: ELSEVIER SCIENCE
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Public țintă
Primary Market: Quality Managers and InspectorsSecondary Market: Students on CE Conformity Marking courses
Cuprins
1.
BACKGROUND
TO
THE
NEW
APPROACH
DIRECTIVES:
European
Directives;
Transition
Period
and
Overlapping
of
Directives;
Application;
Mutual
Recognition
Agreements/European
Conformity
Assessment
Protocols;
Types
of
Directives
and
Standards;
Concurrent
Application
of
Directives;
Aim
of
Standardisation;
International
Standardisation;
Harmonised
European
Standards;
Revision
of
Harmonised
Directives;
Management
of
the
List
of
Standards;
Recognition
of
European
Standards.
2.
STRUCTURE
OF
NEW
APPROACH
DIRECTIVES:
Articles;
Adoption
of
New
Approach
Directives;
Transposition
of
New
Approach
Directives;
Advisory
Committee;
Review
and
Reporting;
Transitional
Provisions;
Repeal;
Entry
into
Force.
3.
STRUCTURE
OF
THE
CE
CONFORMITY
MARKING
DIRECTIVE
(93/465/EEC):
Main
Part;
General
Guidelines;
Conformity
Assessment
Modules
-
Short
Description;
Choice
of
Module;
CE
Marking;
Industrial
Product
Type
conformity;
Competent
Authority;
Notified
Bodies;
Essential
Standards
for
Notified
Bodies;
Relevant
Standards
of
the
EN45000
Series
for
Each
Module;
Notified
Bodies
Tasks
Under
Each
Module;
Requirements
of
the
Various
Directives
affected
by
CE
Marking;
Content
of
the
Directives;
Conformance;
Principle
Directives;
Other
Directives;
Medical
Devices
-
in
vitro
diagnostics
(COM
(95)
130)
180;
Other
Directives
Associated
with
the
CE
Marking
Directive.
4. GAINING OF CONFORMITY: Self Declaration; Voluntary Certification; Mandatory Certification; The 5 Steps to Conformity; Quality Management System; Conformity Assessment Procedures; Conformity requirements of each Module; Conformance Requirements of New Approach Directives; Manufacturers; Manufactuer's Tasks Under Each Module; Basic Requirements of manufacturers of Industrial Products; Registration of manufacturers; EC Verification; Design and Construction Requirements; Index.
4. GAINING OF CONFORMITY: Self Declaration; Voluntary Certification; Mandatory Certification; The 5 Steps to Conformity; Quality Management System; Conformity Assessment Procedures; Conformity requirements of each Module; Conformance Requirements of New Approach Directives; Manufacturers; Manufactuer's Tasks Under Each Module; Basic Requirements of manufacturers of Industrial Products; Registration of manufacturers; EC Verification; Design and Construction Requirements; Index.