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OUR GLOBAL NETWORK AND CAPABILITIES
Global ATIC Business with over 42,000 Employees
Global Global
Market Market
Leader in Leader
Assurance in TIC
3,000 1,000+
laboratories
auditors
and offices
100,000 100+
audits countries
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MORE THAN 100 COUNTRIES, WITH 1,000 LOCATIONS
& 42,000 EMPLOYEES, DELIVERING TOTAL QUALITY SOLUTIONS
Trade
Inspection Certification
Resources
Industrial
Household Medical (Mechanical
ATEX/ TDE/
HVAC/R Lighting Equipment,
Appliance Devices Machinery,
UPS, Switches, Hazloc ASTA
Robots, Etc.)
Energy Renewable
IT/AV/ Connected Storage Energy Power Functional
Batteries World (Power supply, (Photovoltaic,
Tool Safety
Battery, Charging Solar Inverter
pile) Wind Power)
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© Intertek Group
INTERTEK CERTIFICATION AND
ACCREDITATION MARKS
PRODUCT LINE
• Machinery • Inverters
• Pumps • Robotics
• Power Equipment •
• S mark
Our engagement level starts at the stage of product design and prototype with Design Review, Gap Analysis
Developmental Assistance and perform critical tests as per the reference standard to evaluate the compliance level while ascertaining the
deviations.
Intertek’s testing and certification services support the quality, performance, regulatory compliance, safety,
Testing & Certification benchmarking, evaluation, validation, analysis, and other requirements for products, components, raw
materials, sites, and facilities.
Our customized training services ensure your workforce’s competencies on regulatory compliance
Training
requirements with respect to your product portfolio.
Independent third-party inspections help clients protect their financial, branding and legal interests
Inspection
throughout the entire supply chain - from raw materials and finished goods to plant facilities and assets.
CE MARKING
CE stands for Conformitée Européenne, which, translated literally, means “European Conformity”. A product
bearing the CE Marking accompanied with the right formalities can be traded in every country of the European
Economic Area.
The European Economic Area (EEA) is formed by the fifteen Member States of the European Union (EU), viz:
Austria, Belgium, Denmark, Finland, France, Germany, Greece, Ireland, Italy, Luxembourg, the Netherlands,
Portugal, Spain, Sweden and the United Kingdom as well as Iceland, Norway and Liechtenstein (members of the
European Free Trade Association (EFTA)).
Products with a relatively low risk, the producer himself may declare that the product meets the essential
requirements of the corresponding directive. This process is called the internal manufacturing inspection. This
situation involves a process of self-certification and the importer meets his responsibility by drawing up the EC
declaration of conformity and affixing the CE Marking to the product.
Products with a higher risk have to be audited by an external inspection body (Notified Body). The European
Commission has developed several standard modules for these procedures to audit these products for oneself or
to have them audited. These procedures are officially known as conformity assessment procedures.
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Process of CE marking
What is the definition and role of a Nationally Recognized Testing Laboratory (NRTL)?
• OSHA seeks to prevent accidents through assuring the safety of products used by
US workers. NRTLs are private sector organizations that are recognized by OSHA to
perform this safety assurance.
• OSHA recognizes testing organization’s capabilities to test and certify specific types
of products for safety.
Tests products to
applicable published
standards
Provides ongoing
certification & mark for
products that meet the
determined standards
WHO ARE THE NRTLs?
https://www.osha.gov/dts/otpca/nrtl/
Perception: Reality:
Standards = Marks Standards ≠ Marks
Any NRTL recognized to test to a particular
“This product must be certified to UL471 and
standard (such as UL471) may do so and issue its
therefore requires a UL certification mark.”
own proprietary certification mark.
www.intertek.com/ETLdirectory
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CERTIFICATION PROCESS
Process of ETL Mark
Contract process
Required Evaluating Alternatively
Product Commercial Sample
Scope and Test at Cust
details to Commercial Agreement Submission location
be shared
DIFFERENT METHODS
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ETL RECOGNITION
www.intertek.com 26
ETL CLASSIFICATION
• Compliance to certain aspects of standard while not
evaluating other aspects
• Case 1: Medical product that meets the safety
requirements (but performance is not evaluated which is
equally important for end user)
• Case 2: Electrical safety, but not physiological effects or
treatment effectiveness
• Allows manufacturer to label production (with known risk or
understanding allowed by authorities)
• Requires quarterly follow-up inspection
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FIELD LABELING (USA)
• Field labelling allows for on-site product compliance
evaluation.
• In some cases, a product may not have been listed due to error
and an urgent certification is required in time for product
installation.
• Capital Good which can run only after erecting . - that product
may not be operated until all applicable product safety
requirements have been met.
• Labelling is conducted only at installation location (preliminary
inspection may occur anywhere)
• Evaluation required for each product/ unit.
• No follow-up service surveillance
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CANADIAN SPECIAL INSPECTION
CANADIAN SPECIAL INSPECTION
• Canadian National Model Code SPE-1000 (electrical
equipment) or
• SPE -3000 (medical Equipments)
• Products found to comply are labelled on the spot with the
ETL Mark.
• Evaluation and labelling can occur at factory, Intertek lab,
distributor, or final use site
• Faster than listing, but with reoccurring cost per unit
• Evaluation required for each product by engineer
• No follow-up service surveillance
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Process of ETL Mark
Final
Construction Addressing NC Shipment assessment by Issuance of
evaluation in points by to Final Intertek Compliance
India Manufacturer location Canada
Contract process
Required Evaluating
Product Commercial Sample Issuing
Scope and
details to Commercial Agreement evaluation letter report
be shared
TESTING STANDARDS
TESTING STANDARDS
Common Standards for Machinery
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©2018 INTERTEK ALL RIGHTS RESERVED. No reproduction of this material is allowed without written
permission of Intertek. Contact icenter@intertek.com for additional inquiries.