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SGS Product Conformity Assessment
 
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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: 3334 SGS
Conformity Assessment: A Process
 
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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
 
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Chapter 3 of the "Consumer Product Safety in Canada" orientation module.
Views: 417 StandardsCanada
Conformity Assessment: The Perspective of Product Designers
 
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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/
What is conformity assessment?
 
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In just 1 minute, get an overview of conformity assessment with Sean MacCurtain, chairman of ISO's expert committee on it.
Views: 5954 ISO
The 5 most important steps to CE certification - The EU medical device approval process
 
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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 You find the checklist mentioned in the video and additional information in our starter-kit: https://www.johner-institute.com/starter-kit/
Views: 4039 Johner Institute
The Value of Conformity Assessment for Different Players
 
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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/
What is a Declaration of Conformity?
 
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What is a Declaration of Conformity? Find out more on our website: http://www.tuv-sud.co.uk/uk-en/activity/product-certification/european-approvals/ce-marking
Week 5.2 Introduction to conformity assessment procedures
 
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Introduction to conformity assessment procedures for medical devices
Accredited Once, Accepted Everywhere.
 
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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: 14671 IAFandILAC
CE Marking - practical approach guide
 
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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.
Product Compliance Requirements on Amazon: Video Tutorial
 
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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 liked this video, please visit our page to get your free eBook: https://www.chinaimportal.com/ebook
Views: 1868 ChinaImportal.com
Developing Boating Skill Course Conformity Assessment Processes
 
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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: 75 NASBLASafeBoating
RGL3300 L6 Standardization and Conformity Assessment
 
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Lecture 6 - Post Market Assessment Course: Regulation of Hazardous Chemical Products
Views: 7 Thomas Conway
IHE Webinar Conformity Assessment
 
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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: 290 videoIHEeurope
Conformity Assessment for New Standards.wmv
 
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Conformity Assessment for New StandardsAS5553 and AS6081 Counterfeit Avoidance, Mitigation, Detection, and Disposition.
Views: 380 toddkramer1
Chapter 4 - Impacts of conformity assessments on the marketplace
 
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Chapter 4 of the "Consumer Product Safety in Canada" orientation module.
Views: 147 StandardsCanada
Conformity Assessment Programmes
 
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What is involved in getting through with Conformity Assessment programme? The presentation talks about the cases of Kenya, Tanzania and Uganda.
Views: 81 Eximdesk
FAQ of Product Certifications for China Importing And Amazon Selling
 
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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: 1673 Jingsourcing
DMD05_1 - Conformity Assessment
 
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Table of Contents: 00:09 - Repetition fra sidst 07:33 - Conformity Assessment 13:10 - IX: Fuld kvalitetssikring 15:10 - Kvalitetssikringselementer 30:25 - X: EC-Type Examination 32:36 - XI: Production/product verification 36:31 - Demo af MDR annex IX-XI
Views: 21 Samuel Thrysøe
SIEMIC News - Gabon’s Conformity Assessment System for Products, Processes and Services
 
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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/
Bureau Veritas - Transforming conformity assessment with 3DEXPERIENCE - Dassault Systèmes
 
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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: 600 Dassault Systèmes
6/22 | Standards & Conformity Assessment Schemes | CIS 2017
 
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Full title: Standards & Conformity Assessment Schemes: Increasing Trust in Digital Identity Systems? Andrew Hughes
Views: 45 Identiverse
IVD Australia: Obtaining a TGA Conformity Assessment Certificate for IVD devices
 
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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: 127 WMDO
SGS Profile
 
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Discover the SGS Highlights
Views: 1854 SGS
Protocol on the Conformity Assessment and Acceptance of Industrial Products (known as ACAA).mp4
 
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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: 83 David Martin
EU-Israel agreement on conformity assessment and acceptance of industrial products
 
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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: 94 Charles Tannock
ISO Benefits -Conformity Assessment Body
 
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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
Procedures for conformity assessment with technical regulations on medical products in Ukraine
 
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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: 122 Improve Medical
SGS Exporter Portal
 
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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: 5121 SGS
4POP Products Forum | Indonesia | Shirley Dewi, IAPMO
 
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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.
EU-Israel Agreements on Conformity Assessment and Acceptance of Industrial Products.mp4
 
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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
Standards harmonization and conformity assessment  programme
 
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The standards harmonization and conformity assessment programme has improved efficiency at the borders .
SIEMIC News - South Korea’s New Conformity Assessment Criteria for Broadcast & Telecom Equipment
 
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SIEMIC Website: http://www.SIEMIC.com Email: [email protected] Phone Number: 408 - 526 - 1188 Location: 775 Montague Expressway, Milpitas, CA 95035
What is NOTIFIED BODY? What does NOTIFIED BODY mean? NOTIFIED BODY meaning & explanation
 
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What is NOTIFIED BODY? What does NOTIFIED BODY mean? NOTIFIED BODY meaning - NOTIFIED BODY definition - NOTIFIED BODY explanation. SUBSCRIBE to our Google Earth flights channel - https://www.youtube.com/channel/UC6UuCPh7GrXznZi0Hz2YQnQ Source: Wikipedia.org article, adapted under https://creativecommons.org/licenses/by-sa/3.0/ license. A notified body, in the European Union, is an entity that has been accredited by a Member State to assess whether a product to be placed on the market meets certain preordained standards. Conformity assessment can include inspection and examination of a product, its design, and the manufacturing environment and processes associated with it. For example, a notified body may designate that a medical device conforms to the E.U. Medical Devices Directive, which defines the standards for medical devices. With this Declaration of Conformity, the manufacturer can label the product with the CE Mark, which is required for distribution and sale in the E.U. Additionally, the E.U. member state accrediting the notified body will then inform the European Commission that the product complies with set standards (or not). More generally, a notified body is an independent, accredited body which is entitled by an authorized accrediting body. Upon definition of standards and regulations, the accrediting body may allow a notified body to provide verification and certification services. These services are meant to ensure and assess compliance to the previously defined standards and regulations, but also to provide an official certification mark or a declaration of conformity. The notified bodies system used by the European Union has been publicly criticized in some capacity since at least 2008 for issues such as: "a lack of uniformity in certification procedures and in the application of harmonised standards"; "the varying levels of expertise among notified bodies," including "differences in test results"; and "encouraging 'forum shopping' by sponsors to identify those notified bodies with the most lax operating standards." Discussion of further expanding coordination groups of notified bodies for different product areas, improving marketing surveillance, and making participation in standardization and coordination activities mandatory began within E.U. member states. However, more criticism would arise out of the Poly Implant Prothèse (PIP) scandal in early 2010, when media revealed that the French manufacturer of silicone gel breast implants had been using unapproved in-house manufactured industrial-grade instead of medical-grade silicone for most of its implants. Investigators also brought criticism down on notified body TÜV Rheinland for issuing a certificate of quality for a production process that didn't include the in-house industrial-grade silicone. However, TÜV stated "its remit was to check the production process, not the content of the silicone." The revelation had a ripple effect, causing both more criticism about the responsibilities of notified bodies and the regulatory process in general and more corrective action. The Central Management Committee was created in September 2010 "to develop the effectiveness of the regulatory system on medical devices in the E.U. by improving decision making among the national regulatory authorities." Then in February 2012, European Health and Consumer Policy Commissioner John Dalli called upon E.U. member states to take a hard look at the regulatory system, including how notified bodies play a part. His recommendations included properly verifying whether a notified body is capable of accurately assessing medical devices, improving how conformity assessments are conducted, and developing tools to enhance medical device traceability. The European Commission acted, that September revealing its proposed changes to medical device regulation, including expanded requirements on notified bodies, to be published in 2014 and go into effect in 2017. However, the Commission also opted to instate additional reforms — separate from its draft regulations — that would go into effect much sooner, asking notified bodies to perform unannounced visits to manufacturers and expand their device testing standards. At the same time the NB-MED (European Forum of Notified Bodies Medical Devices) coordination revised their Code of Conduct due to criticism.....
Views: 142 The Audiopedia
Ethiopia Conformity Assessment Enterprise
 
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5 min documentary production and 1 MIN Tv ad.
Views: 111 PhatronCGI
A summary of supplying therapeutic goods in Australia
 
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If you are thinking of supplying a therapeutic good, then you are a potential sponsor. To help you get started, watch this video to find out: * the six steps you need to follow when considering making an application to the TGA * where to find relevant information about different types of goods * what legal and financial responsibilities you need to be aware of * where to get more information on the regulatory process. * Make sure you also read the Overview of Supplying Therapeutic Goods in Australia.
Views: 12918 TGA Australia
SIEMIC News - SIEMIC is First in Israel Conformity Assessment Bodies and Test Labs for Telecom!
 
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SIEMIC Website: http://www.SIEMIC.com Email: [email protected] Phone Number: 408 - 526 - 1188 Location: 775 Montague Expressway, Milpitas, CA 95035
Сергей Колдаев о сертификации
 
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Вопрос международной адаптации и оценки соответствия продукции крайне важен для экспортеров. Основные барьеры лежат в области отличий законодательных требований РФ и других стран. Что стоит учесть?

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