Home
Search results “Product conformity assessment”
SGS Product Conformity Assessment
 
02:34
SGS Product Conformity Assessment (PCA) is a solution designed to ensure that products meet the specific requirements set by a regulatory authority in the importing country. The solution consists of verifying product’s compliance with the requirements of applicable standards and technical regulations following a review by SGS product specialists, of reports from verification activities such as laboratory testing, physical inspection and factory audits. Conformity of products is evidenced by the issuance of a Certificate of Conformity, a document that is mandatory for customs clearance.
Views: 2558 SGS
Conformity Assessment: The Perspective of Product Designers
 
06:02
Gordon Gillerman of NIST discusses different scenarios in which companies would have benefited from considering conformity assessment requirements earlier on in the product design phase. Excerpted for the IEEE Standards Education MOOC, "Innovation and Competition: Succeeding through Global Standards" from 2016. The IEEE Standards Association (IEEE-SA) is a leading consensus building organization that nurtures, develops and advances global technologies, through IEEE. We bring together a broad range of individuals and organizations from a wide range of technical and geographic points of origin to facilitate standards development and standards related collaboration. With collaborative thought leaders in more than 160 countries, we promote innovation, enable the creation and expansion of international markets and help protect health and public safety. Collectively, our work drives the functionality, capabilities and interoperability of a wide range of products and services that transform the way people live, work and communicate. Visit IEEE-SA Website: http://standards.ieee.org/
Conformity Assessment: A Process
 
05:05
Rudi Schubert of the IEEE Standards Association discusses the role of conformity assessment in demonstrating that products or services meet the specific requirements described in standards. Excerpted for the IEEE Standards Education MOOC, "Innovation and Competition: Succeeding through Global Standards" from 2016. The IEEE Standards Association (IEEE-SA) is a leading consensus building organization that nurtures, develops and advances global technologies, through IEEE. We bring together a broad range of individuals and organizations from a wide range of technical and geographic points of origin to facilitate standards development and standards related collaboration. With collaborative thought leaders in more than 160 countries, we promote innovation, enable the creation and expansion of international markets and help protect health and public safety. Collectively, our work drives the functionality, capabilities and interoperability of a wide range of products and services that transform the way people live, work and communicate. Visit IEEE-SA Website: http://standards.ieee.org/
Chapter 3 - Conformity assessment for consumer product safety
 
03:12
Chapter 3 of the "Consumer Product Safety in Canada" orientation module.
Views: 370 StandardsCanada
What is conformity assessment?
 
01:06
In just 1 minute, get an overview of conformity assessment with Sean MacCurtain, chairman of ISO's expert committee on it.
Views: 5666 ISO
The 5 most important steps to CE certification - The EU medical device approval process
 
08:46
This video introduces the Europan medical device regulations, in particular the Medical Device Regulation MDR, the conformity assessment procedures (sometimes referred to as "certification process") and the medical device classification. It explains when an ISO 13485 certified quality management system is required and which are the most relevant documents manufacturers have to compile
Views: 1929 Johner Institute
The Value of Conformity Assessment for Different Players
 
08:36
Yatin Trivedi of Aricent, Inc. discusses the value of conformity assessment from different perspectives, including those of design engineers, regulators, purchasing agents, and lawyers. Excerpted for the IEEE Standards Education MOOC, "Innovation and Competition: Succeeding through Global Standards" from 2016. The IEEE Standards Association (IEEE-SA) is a leading consensus building organization that nurtures, develops and advances global technologies, through IEEE. We bring together a broad range of individuals and organizations from a wide range of technical and geographic points of origin to facilitate standards development and standards related collaboration. With collaborative thought leaders in more than 160 countries, we promote innovation, enable the creation and expansion of international markets and help protect health and public safety. Collectively, our work drives the functionality, capabilities and interoperability of a wide range of products and services that transform the way people live, work and communicate. Visit IEEE-SA Website: http://standards.ieee.org/
Procedures for conformity assessment with technical regulations on medical products in Ukraine
 
37:23
Introduction of Ukrainian Technical Regulations. Step-by- step description of the procedure. What is the object of the audit? Multi-object enterprise. OBL - OEM Necessary documentation. Audit process. The most frequent non-conformities.
Views: 90 Improve Medical
CE Marking - practical approach guide
 
45:19
This presentation is intended to provide a practical approach guide to what you need to know about the CE marking requirements for electrical and electronic equipment placed on the European Market. The material is intended to inform those that do not already understand CE marking requirements and to clarify and reinforce the understanding of those already familiar with the concepts. This presentation is intended for anyone involved in the design, development, production and selling of products that are placed on the European market. This includes, design engineers, project managers, engineering managers, approvals engineers, quality managers, sales managers. In particular those who sign the Declaration of Conformity.
Protocol on the Conformity Assessment and Acceptance of Industrial Products (known as ACAA).mp4
 
02:45
David Martin MEP and member of the European Parliament's International Trade Committee today condemned the approval of a trade upgrade between the EU and Israel. The Protocol on the Conformity Assessment and Acceptance of Industrial Products (known as ACAA) will make it easier for Israel to export pharmaceutical products to the European Union. The European Parliament had previously challenged the Commission on the checks to ensure goods from the Occupied Territories could not enter the European Union (EU) under this Protocol. David argues that approving this Protocol is incompatible with recent European Parliament and EU declarations denouncing Israeli activity in the Occupied Territories.
Views: 81 David Martin
IHE Webinar Conformity Assessment
 
01:01:34
This webinar is organized around the IHE-Europe Connectathon In Luxemburg, 1st section IHE Conformity Assessment Strategic Objectives Charles Parisot, Member IHE International CAsC Committee 2nd section Application for the Conformity Assessment Testing Session by Eric Poiseau - Technical Manager, Raphaëlle Batogé – Quality Manager
Views: 280 videoIHEeurope
FAQ of Product Certifications for China Importing And Amazon Selling
 
04:26
Our Website: https://jingsourcing.com/ Request A Free Quote Of Your Product Now: https://jingsourcing.com/submit-ticket/ Contact Us: [email protected] If you want to import from China to US or Europe, no matter you sell on Amazon or some street stores, it’s so important for you to understand the compliance certifications for your products. Why? The custom will hold your products, or even destroy them if you can’t offer any certifications to prove your products have reached the local product safety standard. Most importers don’t know much about what kind certifications they need for custom clearance or Amazon selling. Even a lot of Chinese manufacturers may give you wrong information, because usually they are not the expert at the point. That’s why we decided to make this video, to share some basic knowledge of compliance certifications. In the 1st part of this video, I explained who will need you to provide certifications, and also in what kind circumstance you can avoid to provide. In the 2nd part, I explained what kind of bad consequence you maybe have, if you don’t have certifications, or you can’t provide it in time. A very good case is also shared, to explain Amazon’s strict solution for no certifications. In the 3rd part, I made a list of certifications that you probably need for importing to US. In the 4th part, I shared my experience about how you can get product certifications.
Views: 1058 Jingsourcing
CE Machinery Marking
 
53:03
CE marking is a process that allows manufacturers to declare that their product complies with all applicable European Community Directives. A declaration of conformity, issued by the manufacturer or its authorised representative, allows the product to be marked with the CE mark and offered for sale in the EU. Machinery may not be offered for sale in the EU without CE marking unless it falls within one of the Machinery Directive exclusion categories. CE marking according to the requirements of the Machinery Directive is mandatory for machines offered for sale in the European Union. The CE marking process is often relatively simple, but requires an interpretation of the requirements of the directives applicable to the product to be marked and, in the case of the Machinery Directive, a risk assessment against the applicable Essential Health and Safety Requirements. This webinar introduced the European Machinery Directive, other applicable Directives and the CE marking process to help you meet your legal requirements.
CE Marking of Medical Devices - Technical Documentation
 
28:18
In the context of EC type and EC Design examinations, LNE / G-MED provides Medical Device Manufacturers with a list of the elements to be supplied for the CE marking of their medical devices. The list shall specify the content of the Dossiers to be submitted to the Notified Body as part of their conformity assessment. LNE / G-MED update this list and through this webinar, inform Medical Device Manufacturers, of the changes to be taken into account for future dossiers submissions. The webinar addresses the following main points: Update /creation of the list of elements to be provided for the CE marking of a Medical Device in the context of: • An Initial evaluation • Evaluation of a change • Evaluation of a renewal
Views: 771 GMED
IVD Australia: Obtaining a TGA Conformity Assessment Certificate for IVD devices
 
02:47
Course Description: This course describes conformity assessment and examines the process for obtaining a Conformity Assessment Certificate from the Australian Therapeutic Goods Administration (TGA), including the timeframes for assessment. It also explains what happens once an application is deemed successful or not and the ongoing responsibilities of the manufacturer after a certificate has been obtained. Learn more at: http://www.wmdo.org/course-detail.aspx?id=153
Views: 121 WMDO
6/22 | Standards & Conformity Assessment Schemes | CIS 2017
 
23:45
Full title: Standards & Conformity Assessment Schemes: Increasing Trust in Digital Identity Systems? Andrew Hughes
Views: 39 Identiverse
Developing Boating Skill Course Conformity Assessment Processes
 
01:06:17
Developing Boating Skill Course Conformity Assessment Processes Based on National Skill Standards Tuesday, December 1, 2015 (2:00 PM ET) As part of the 2016 "Spring Aboard - Take a Boating Course" national marketing campaign, a process is being developed to verify on-water skills courses which meet the voluntary national boating skill standards. Verified courses will be marketed as part of the Spring Aboard Campaign along with knowledge courses previously approved by NASBLA. This session will cover what is meant by 'conformity assessment' as defined by the American National Standards Institute (ANSI). With funding from a current U.S. Coast Guard grant, a process will be implemented to verify a course as meeting recognized on-water skill standards for power, sail, or human-propelled boating courses. Successful completion of the conformity assessment process will result in the award of a 'Verified Course' mark indicating "This Course Content meets National Boating Skill Standards as Recognized by the U.S. Coast Guard." *This is a repeat of the session presented on September 15, 2015 at the NASBLA Annual Conference in Wichita, Kansas.
Views: 62 NASBLASafeBoating
Bureau Veritas - Transforming conformity assessment with 3DEXPERIENCE - Dassault Systèmes
 
02:16
Bureau Veritas - Transforming conformity assessment with 3DEXPERIENCE - Dassault Systèmes. Bureau Veritas uses Dassault Systèmes’ 3DEXPERIENCE platform to implement digital continuity from initial specifications to transport, installation and operation of pressure equipment in a nuclear facility. A single integrated platform of product information enables stakeholders to access and act on the latest version of product data, thereby accelerating certification cycle times and traceability. Learn more: https://ifwe.3ds.com/energy-process-utilities Don’t forget to subscribe: https://goo.gl/bDS7oS Dassault Systemes official website: http://www.3ds.com/ Follow us! Facebook: https://www.facebook.com/DassaultSystemes Twitter: https://twitter.com/Dassault3DS Linkedin: https://www.linkedin.com/company/dassaultsystemes
Views: 431 Dassault Systèmes
How To Get CE Marking Certification For My Product?
 
05:11
How to achieve CE mark approval, CE testing and meet all CE mark requirements, for my product? There are a series of steps outlined below for CE mark approval. Depending on your product and the nature of the risks it presents: Number 1. Determine if any directives apply to your product. If more than one applies you will have to comply with all of them. Number 2. Determine the extent to which your product complies with the essential requirements for design and manufacturing in the applicable directive(s). Number 3. Choose the conformity assessment procedure from the options (modules) called out by the directive for your product. There are several modules available for the Conformity Assessment Procedures as listed below: Module A: internal production control Module Aa: intervention of a Notified Body Module B: EC type-examination Module C: conformity to type Module D: production quality assurance Module E: product quality assurance Module F: product verification Module G: unit verification Module H: full quality assurance The directives often use a series of questions about the nature of your product to classify the level of risk and refer to a chart called "Conformity Assessment Procedures". The chart includes all of the acceptable options available to a manufacturer to certify their product and affix the CE Marking. A Notified Body is usually able to offer some of the services required: Number 1. Product testing Number 2. Type examination certificate issue Number 3. Technical File and design dossier evaluation Number 4. Surveillance of product and quality system Number 5. Identification of standards If your products need to be certified by a Notified Body, then you will need to do as the follows: Number 1. Select the applicable product standards and test methods for your product and select a Notified Body. Number 2. Establish an Authorized Representative in the European Union for your product. Some directives require that a manufacturer designates in the European Union an authorized representative to produce Technical File in a timely fashion when called upon to do so. The CE Marking itself is not meant to provide details about the product to Surveillance Authorities. Technical File: The directives require for many products that a Technical File be prepared by the manufacturer. The Technical File holds information that verifies that the testing was conducted properly and that the product complies with applicable standards. Number 3. Prepare a Declaration of Conformity. The Declaration of Conformity must contain information adequate for tracing the product back to the manufacturer or the authorized representative in the European Union. It may include a list the directives and standards that your product conforms to, product identification, the manufacturer's name, address, and signature. Number 4. Register your product in EU Many products, for instance, Class I Medical Devices, are required to be registered in the EU and, if proved, get a Certificate of Registration. Without this Certificate of Registration, the products are NOT allowed to be affixed with the CE Marking and be placed on the market. Number 5. Affix the CE Marking to your product. There are specific rules to adhere to for the CE Marking. These rules address the size and location of the Marking; affixing the CE Marking to products, packaging and material or documents shipped with the product; and specific limitations on when and who is permitted to affix the CE Marking Thanks For Watching EU-CERT has Certified thousands of products to support CE Marking certification Declarations of Conformity DoC for equipment safety, electromagnetic compatibility, and energy efficiency. Contact us today to tap the experience and skill of the EU-CERT Certification Expert team. You can feel free to call our CE Certification Specialists – Free 24 Hour Advice and Support https://eu-cert.org/how-to-get-ce-marking-certification-for-my-product/ Searches related to How To Get CE Marking Certification For My Product? how to get CE certification CE marking self-certification how to get CE certification in India CE certification cost CE marking self-certification pack what products need CE marking CE marking guide CE marking exemptions
Views: 277 ECT European
Product Compliance Requirements on Amazon: Video Tutorial
 
09:20
Importing from Asia and selling on Amazon? Watch this video and learn how to comply with all safety standards and submit the right documents so you don't get suspended. If you found this video useful, click here to learn how we can help you: https://www.chinaimportal.com/all-categories/
Views: 1326 ChinaImportal.com
4POP Products Forum | Indonesia | Shirley Dewi, IAPMO
 
13:21
Presentation given at the Four Pillars of Plumbing forum held 17 May, 2018 in Ontario, California. Plumbing Products Conformity Assessment in Indonesia. Shirley Dewi is the Senior Vice President of Quality Assurance and Client Services for IAPMO R&T. She is responsible for maintaining accreditations for IAPMO, including overseeing the operations of ISO Management Systems Registration Services and the operations of Indonesia facility. She is based in IAPMO’s world headquarters in Ontario, Calif., USA. Prior to joining IAPMO in 2007, Dewi was the Quality Manager for Bericap North America. She has been in quality-assurance industry for more than 17 years and in the third-party conformity assessment industry for more than 10 years. Dewi is one of IAPMO’s key staff members in the Water for Indonesia Now (WIN) Project, an effort supported by the United States Agency for International Development (US AID) and the International Trade Administration (ITA) to promote plumbing system standardization to ensure safe water delivery for Indonesian citizens. She is also one of the expert sources in the development of SNI 8153:2015 (Plumbing Systems for Buildings). Dewi earned her business management degree from California State Polytechnic University Pomona in 1998. She is the liaison for IAPMO with various accreditation bodies and government agencies, such as the American National Standards Institute (ANSI), Standards Council of Canada (SCC), Entidad Mexicana de Acreditación (EMA), ANSI-ASQ National Accreditation Board (ANAB), Komite Akreditasi Nasional (KAN), U.S. Environmental Protection Agency WaterSense program, U.S. Environmental Agency Energy Star program, the city of Los Angeles and the state of Florida. She also serves as the voting member on the American National Standards Institute (ANSI) Accreditation Committee.
SIEMIC News - Gabon’s Conformity Assessment System for Products, Processes and Services
 
02:23
SIEMIC Website: http://www.SIEMIC.com Email: [email protected] Phone Number: 408 - 526 - 1188 Location: 775 Montague Expressway, Milpitas, CA 95035 AGANOR website: http://www.aganor.ga/
Standards harmonization and conformity assessment  programme
 
00:13
The standards harmonization and conformity assessment programme has improved efficiency at the borders .
An overview about Bureau Veritas Certifications's footprint in conformity assessment
 
02:16
Mr Ramesh Koregave, Director, #Certification Business, South Asia Region, presenting the Bureau Veritas's footprint in the region in conformity assessment and certification of organizations against a wide range of International #Standards on Management Systems covering #Quality (#ISO #9001), #Environment (ISO #14001),#Occupational #Health & #Safety (ISO #45001),#Information #Security ( ISO #27001),#Food #Safety (ISO #22000), and Bureau Veritas' own standards on School Safety (SHSMS), Green and Clean Hospitals (GnC), Responsible Critical Care Units (ResCCU), Green OT, #PDQ (pharmacie de qualite) etc. BUREAU VERITAS, is one of the leading training service providers in India and over the years have developed a suite of training courses, delivered by experienced and competent trainers. We at Bureau Veritas offer more than 360 training modules including 20 IRCA certified Auditor /Lead Auditor/Auditor conversion training courses. We conduct more than 850 training courses every year at more than 30 locations across the country, thus helping over 10,000 professionals from wide spectrum of industry hone their skills and enhance their competence. Our training portfolio covers management system standards, Business Excellence,soft skills, financial services, safety, analytical sciences, laboratory practices, civil engineering and construction management leading to a large variety of training courses ranging from overview sessions, Internal Auditor courses, Auditor Conversion course, Lead Auditor courses, and Technical workshops to specialized workshops and personnel qualification and certification programmes. The courses provide a total package of the approach and enable implementation. They are also highly interactive with real world examples, case studies, exercises, question & answer session and experience sharing by the Tutor. Our courses also provide an opportunity for participants from different sectors and industry experience and background to interact with others and share their experience and in the process, enrich their knowledge. All our courses are available both in open-house and in-house formats. Requests for in house training courses are entertained keeping in conformance to Accreditation Body requirements. Our Website-: https://training.bureauveritas.co.in/ Follow us on-: facebook-:https:https://bit.ly/2N3ZaDT Linkedin-: https://bit.ly/2oMaZzW Twitter-: https://bit.ly/2MoKv0D
ISO Benefits -Conformity Assessment Body
 
02:51
This presented Video will help you to understand How ISO Standards can benefit you, your organisation, How you can run a successful business. ISO Is not only Standard but its full Management system available for everyone that can save you from losses and increase productivity
Conformity Assessment for New Standards.wmv
 
51:03
Conformity Assessment for New StandardsAS5553 and AS6081 Counterfeit Avoidance, Mitigation, Detection, and Disposition.
Views: 365 toddkramer1
SGS Exporter Portal
 
02:28
A faster, easier way to navigate the product conformity assessment process SGS Exporter Portal, our new web-based app, simplifies the PCA process. It allows you to request a certificate of conformity, registration or license online whenever you wish, and then complete your application at your own pace. SGS experts are on hand to clarify any issues, so you can ensure the process runs smoothly.
Views: 3951 SGS
Accredited Once, Accepted Everywhere.
 
02:03
Accreditation is the independent evaluation of conformity assessment bodies against recognised standards to carry out specific activities to ensure their impartiality and competence. Through the application of national and international standards, government, procurers and consumers can have confidence in the calibration and test results, inspection reports and certifications provided. Accreditation bodies are established in many countries with the primary purpose of ensuring that conformity assessment bodies are subject to oversight by an authoritative body. Accreditation bodies, that have been evaluated by peers as competent, sign arrangements that enhance the acceptance of products and services across national borders, thereby creating a framework to support international trade through the removal of technical barriers. These arrangements are managed by the International Laboratory Accreditation Cooperation (ILAC), in the field of laboratory and inspection accreditation, and the International Accreditation Forum (IAF), in the fields of management systems, products, services, personnel and other similar programmes of conformity assessment. Both organisations, ILAC and IAF work together and coordinate their efforts to enhance the accreditation and the conformity assessment worldwide.
Views: 14104 IAFandILAC
EU-Israel agreement on conformity assessment and acceptance of industrial products
 
01:29
The ECR Group believes that EU-Israel agreement on conformity assessment (ACA) and acceptance of industrial products has been delayed far too long in this Parliament. This agreement is not about the territorial provenance of pharmaceutical products. It is about the right for competent Israeli authorities to certify medicines that they examine as being up to EU standards. There are already separate stringent EU wide rules about goods arriving from the West Bank and Gaza and what EU tariffs should apply to them. ACA is a technical agreement but has become a highly politicised Israel-bashing exercise which does nothing to facilitate access to high quality and affordable pharmaceutical products for our European consumers
Views: 93 Charles Tannock
Return on Experience from Conformity Assessment Bodies, presented by Arvid Vermote, EY
 
11:23
Return on Experience from Conformity Assessment Bodies, presented by Arvid Vermote, EY @ ETSI Security Week 2017
Views: 153 ETSI
Conformity Assessment Programmes
 
01:13
What is involved in getting through with Conformity Assessment programme? The presentation talks about the cases of Kenya, Tanzania and Uganda.
Views: 78 Eximdesk
EU-Israel Agreements on Conformity Assessment and Acceptance of Industrial Products.mp4
 
01:31
Speaking at a meeting in the European Parliament I led for the British Conservatives in a heated debate on EU-Israel Agreements on Conformity Assessment and Acceptance of Industrial Products. ACAAs are a specific type of mutual recognition agreement based on the alignment of the legislative system and competent authorities of the country concerned with those of the European Union. The EU-Israel ACAA would facilitate the import of high-quality and affordable medicines into Europe, but is being held up in the European Parliament because the legislative process has been hijacked by anti-Israel sentiment.
Views: 78 Charles Tannock
Chapter 5 - What accreditation services does SCC offer?
 
02:59
Chapter 5 of the "Accreditation: Where standards, conformity and quality meet" orientation module. Transcript Chapter 5: What accreditation services does SCC offer? SCC’s Accreditation Services branch delivers accreditation services to Canadian customers working in Canada and abroad, and two international customers doing business in Canada. SCC accreditation recognizes the competence of laboratories and certification bodies. The following kinds of organizations are accredited by SCC under SCC's ISO-based programs: - Testing and calibration laboratories - Management systems certification bodies - Personnel certification bodies - Product, process and service certification bodies - Greenhouse gas validators/verifiers, and - Inspection bodies SCC also offers two Non-ISO-based accreditation programs: - OECD Good laboratory practice facilities, and - Standards development organizations What types of testing laboratories does SCC accredit? SCC accredits: - Food testing - Drinking water testing - Environmental sample testing - Mineral testing, and - Materials testing laboratories What types of management systems does SCC accredit? SCC accredits - Quality - Environmental - Energy - Food safety, and - Occupational health and safety management systems What types of product certification does SCC accredit? SCC accredits: - Electrical - Fire protection - Safety equipment - Energy-efficient, and - Mobile home component product certification What types of inspections does SCC accredit? SCC accredits: - Electrical systems - Medical gas piping systems, and - Commercial gas-fired appliance inspections Why get accredited by SCC? SCC is well-respected in Canada and around the world. As a signatory to the International Accreditation Forum and the International Laboratory Accreditation Cooperation, SCC can assess according to ISO standards and is subject to regular evaluation itself. SCC’s customers can feel confident in the credibility of products, systems and services that SCC accredits in Canada and abroad. SCC consistently delivers high-quality and rigorous accreditation services. For more information about SCC's Accreditation Services, and for listings of SCC-accredited organizations, please visit https://www.scc.ca.
Views: 140 StandardsCanada
Chapter 4 - Impacts of conformity assessments on the marketplace
 
03:48
Chapter 4 of the "Consumer Product Safety in Canada" orientation module.
Views: 133 StandardsCanada
Exporting to Kenya, Uganda & Niger
 
08:24
Helping you comply with export and import requirements. The Governments of Kenya, Uganda & Niger have introduced a Conformity Assessment Programme (CAP) to ensure the quality and safety of products imported into the country. All regulated products that are now shipped to Kenya, Uganda & Niger are subject to certification and must be accompanied with a Certificate of Conformity. In order to help your products clear Customs in these countries all Exporters need to comply with the requirements of the CAP. Failure to comply with the CAP requirements will result in severe delays of the consignment leading to penalties or even the failure of your shipments to clear Customs. The authorities in Kenya, Uganda & Niger may take random samples from imported consignments to verify the compliance of the goods being shipped. Your goods will not clear Customs without a Certificate of Conformity. Intertek Government and Trade Services is authorised to issue these Certificates to Exporters. The Certificate of Conformity confirms that your products comply with all the relevant and required Kenyan, Ugandan & Niger technical regulations and national, regional or international standards.
Views: 2495 IntertekGTS
ISO Standards Training, Assessment and Certification
 
01:16
ODC has designed and implemented "Quality Management system" in accordance with the international standard ISO 17021 (Conformity Assessment - Requirements for bodies providing audit and certification of management systems) ODC acknowledges requirements of some its customers regarding Accreditated certification (Certificate of Registration) / Independent certification (Certificate of Compliance) and hence will have several accreditation options so that customers can take informed decisions. ODC has empanelled qualified trainers, lead auditors / assessors who are equipped to provide customised services from their respective locations. ODC has network of empanelled auditors across India and operates on concept HUB & SPOKE model. For more details please visit us: http://www.odccert.org/
CE MARKING
 
04:18
www.obelis.net Learn about the importance of the CE Marking particularly concerning European compliance and what is required in order to affix the CE Marking to your products. Topics covers: -Complexity of the CE Marking -Steps to obtain the CE Marking -Classification in accordance with the applicable EU Legislation(s) -Identification of the Essential Safety & Health Requirements and proper Conformity Assessment procedures -Building evidence of compliance within Technical Documents (aka EU Dossier) -Certification Procedures -Pre-Market Notification to the Competent Authorities -Affixing the CE Mark -EU Market entry! Please feel free to contact us with any questions! www.ObelisMedical.net/contacts
Views: 3578 Obelis Group
CE मार्क वाला प्रोडक्ट ध्यान से ख़रीदे। What is CE Mark on Electronics। Don't Buy CE Symbol Product
 
03:42
CE मार्क वाला प्रोडक्ट ध्यान से ख़रीदे । What is CE Mark on Electronics Don't Buy CE Symbol Product CE marking (CE Mark) is a certification mark that indicates conformity with health, safety, and environmental protection standards for products sold within the European Economic Area (EEA). The CE marking is also found on products sold outside the EEA that are manufactured in, or designed to be sold in, the EEA. This makes the CE marking recognizable worldwide even to people who are not familiar with the European Economic Area. It is in that sense similar to the FCC Declaration of Conformity used on certain electronic devices sold in the United States. The CE marking is the manufacturer's declaration that the product meets the requirements of the applicable EC directives. The mark consists of the CE logo and, if applicable, the four digit identification number of the Notified Body involved in the conformity assessment procedure. "CE" originated in 1985 as an abbreviation of Conformité Européenne, meaning European Conformity, but is not defined as such in the relevant legislation. The CE marking is a symbol of free marketability in the European Economic Area (Internal Market). Our Video Series - Bullet Train Series - http://bit.ly/2xQD7c7 Indian States Series - http://bit.ly/2xQ4Pke Different Country Series - http://bit.ly/2zzOhPO Hidden Universe( ब्रह्मांड ) Series - http://bit.ly/2yzMYQH Ram Rahim Series - http://bit.ly/2gPM5Mf Pink Whale Series - http://bit.ly/2gSiv94 Blue Whale Series - http://bit.ly/2zkb8Od Rohingya Muslim Series - http://bit.ly/2zmiFfv Our All in one Video Series - http://bit.ly/2ySJ34l All other Whale Series, Blue whale,pink,red, green whale Series - http://bit.ly/2ytQU86 I'm the owner of the audio track(Excluding Music which is royalty free). The videos and Images I've used in this video is purely demonstration purpose only. I've found them through search engine (mostly royalty free). So I'm really grateful to them. If I've used any other's content then i will definitely credit him. Still you've something to say? contact me - [email protected] Music Credit - Carefree by Kevin MacLeod is licensed under a Creative Commons Attribution license (https://creativecommons.org/licenses/by/4.0/) Source: http://incompetech.com/music/royalty-free/index.html?isrc=USUAN1400037 Artist: http://incompetech.com/ Copyright Disclaimer :- Under Section 107 of the Copyright Act 1976, allowance is made for "fair use" for purposes such as criticism,comment, news reporting,teaching, scholarship, and research. Fair use is a use permitted by copyright statute that might otherwise be infringing. Non-profit,educational or personal use tips the balance in favor of fair use.
Views: 4028 Rahasya Live

Montana 1948 conflict essay
School band and orchestra magazine essay contest
Writing the title of an article in essay mla generator
The uk constitution is no longer fit for purpose essay examples
Pandit jawaharlal nehru essay in punjabi