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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: 1867 SGS
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: 5450 ISO
Chapter 3 - Conformity assessment for consumer product safety
 
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Chapter 3 of the "Consumer Product Safety in Canada" orientation module.
Views: 356 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/
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/
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/
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: 269 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: 357 toddkramer1
Standards harmonization and conformity assessment  programme
 
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The standards harmonization and conformity assessment programme has improved efficiency at the borders .
Week 5.2 Conformity assessment procedures for medical devices
 
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Conformity assessment and classification of medical devices
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: 73 Improve Medical
CE Machinery Marking
 
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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.
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: 93 Charles Tannock
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: 38 Identiverse
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/
How To Get CE Marking Certification For My Product?
 
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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: 95 ECT European
Ethiopia Conformity Assessment Enterprise
 
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5 min documentary production and 1 MIN Tv ad.
Views: 90 PhatronCGI
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: 72 Eximdesk
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: 30 The Audiopedia
RETAIL & PRODUCT SAFETY COMPLIANCE & CERTIFICATION
 
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This webinar will provide an overview of NSF International, a public health & safety organization, the retail testing landscape and the product evaluation requirements for the NSF Home Product Certification (HPC) program. Hear how products can achieve this quality distinction that communicates to consumers that your products have met the highest level of product quality, performance, safety and regulatory compliance, and they can trust your products to deliver. Attaining product certification is one way of telling consumers and retailers that your products meet stringent comprehensive requirements. This free informational webinar will cover a broad range of housewares including: Small home electric appliances Cookware Tableware Cutlery & flatware Food storage containers Bakeware Food contact utensils personal beverage containers Barware & accessories Presenters Ashlee Breitner, Business Unit Manager, Food Safety Product Certification NSF International [email protected]
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
CE MARKING
 
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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: 3225 Obelis Group
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.
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: 115 WMDO
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: 81 David Martin
Exporting to Kenya, Uganda & Niger
 
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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: 2255 IntertekGTS
ISO 14040 Product Life cycle Assessment 2015
 
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Introduction to Environmental Management Systems The ISO 14040 series of International Standards emphasise the importance of audits as a management tool for monitoring and verifying the effective implementation of an organisation's quality and/or environmental policy. Audits are also an essential part of conformity assessment activities such as external certification/registration and of supply chain evaluation and surveillance.
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: 126 StandardsCanada
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
Views: 400 Johner Institute
Return on Experience from Conformity Assessment Bodies, presented by Arvid Vermote, EY
 
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Return on Experience from Conformity Assessment Bodies, presented by Arvid Vermote, EY @ ETSI Security Week 2017
Views: 105 ETSI
Intertek GTS Tanzania and Kenya Exporter Guide
 
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Helping you comply with export and import requirements The Governments of Kenya and Tanzania have introduced a Conformity Assessment Programme to ensure the quality and safety of products imported into the country. This programme is called the Pre-Verification of Conformity programme, commonly known as a PvoC. All regulated products that are now shipped to Kenya and Tanzania are subject to certification. Intertek can advise you on what products are regulated.
Views: 363 IntertekGTS
What Is An Accreditation Body?
 
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About ias the international accreditation service. Accreditation body membership of iaf is open to bodies conducting and administering programmes by which they accredit for certification registration quality systems, products, services, personnel, environmental management systems similar conformity assessment declare their common organizations that issue credentials or certify third parties against official standards are themselves formally accredited accreditation (such as ukas); Hence sometimes known 'accredited bodies' the following recognise food safety system scheme fssc 22000, owned foundation 22000 in must apply an has signed multilateral agreement (mla) on product a) a member formal recognition independent body, generally operates according international setting up ina guide opening door for9th june 2017. If you wish to see which bodies have been recently added the list quality assurance unit of mauritius standards bureau is a third party conformity assessment body and accredited as per iso iec 17021 2011 one leading accreditation in united states, ias signatory four primary international organizations that form unified system for greenhouse gas validation verification use or other Accreditation members by nameaccreditation fssc 22000. Accreditation body members by nameaccreditation bodies fssc 22000. List of accreditation bodies globalg. Accreditation frequently asked questions. Apaccreditation bodies unido. Accreditation wikipedia accreditation body members by name iaf. Mauritius standards bureau accreditation body. It is designed to ensure that conformity assessment bodies (e. Based accreditation bodies that are members of major multilateral fora and arrangements such as the international forum (iaf) asi has been appointed body for a range voluntary sustainability standards (vss). Accreditation wikipedia. To certify these standards, a cab must be iso iec 17000 specifies the general terms and their definitions relating to conformity assessment, including accreditation of assessment bodies, below is list all bodies accredited by rva. What is the difference between certification and accreditation? . Nu articles accred_body_members_by_name 52 "imx0m" url? Q webcache. All accredited bodies dutch accreditation council. Ukas is recognised by accreditation the last level of public control in european conformity assessment system. You can also apply filters to this list. Edition 2 the national accreditation board for certification bodies (nabcb) undertakes assessment of and inspection applying as part procedure, they can confirm to an independent body that carry out their activities with technical competence, in process, objective external group examines evaluates ensure it is meets standards published by accrediting bodyan organisation delegated make decisions, on behalf higher education sector, about what ukas? The united kingdom service (ukas). Accreditation bodies directory standards portal. National accreditation board for certification bodiesabout accrediting bodies body analytic quality glossaryaccreditation of conformity assessment european u. Accreditation cofrac comit franais d'accrditation. Googleusercontent search.
Views: 8 E Answers
Traders encouraged to promote product quality standards
 
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Traders encouraged to promote product quality standards. INDUSTRY minister Mike Bimha has appealed to traders to follow consignment-based conformity assessment (CBCA) requirements to limit the inflow of sub-standard products into the country. BY TALENT GUMPO The CBCA programme, which ensures that all listed imported products meet quality, safety, health and environmental standards in line with the World Trade Organisation agreements, was officially launched in Zimbabwe in 2015. In a speech read on the minister’s behalf by Standards Development and Qua... Get Free Subscribe Here: - https://goo.gl/QrjDRC Website: https://goo.gl/UasZwB Twitter: - https://goo.gl/WdWB1i Plus: - https://goo.gl/4viMNi Thanks For Watching. Don't forget LIKE, SHARE and SUBSCRIBE.
Tti Testing Laboratories - An Introduction
 
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Tti is an Internationally accredited ISO/IEC 17025 Testing laboratory with the largest recognized and endorsed testing scope in the country for Textiles, Leather, Restricted Substances, Petroleum Products and Environmental Testing. Tti also has the honor of being the first lab accredited by the US Consumer Product Safety Commission as a Conformity Assessment body for Consumer Safety/ Restricted Chemical testing in Pakistan and till date, Tti still maintains the largest accredited CPSC scope in the region. Tti Testing Laboratories offers a comprehensive spectrum of textile & apparel testing services, testing to a wide range of different mandatory national & international standards of Quality and Consumer Safety including ASTM, AATCC, ISO, BS, CE Marking, CPSC, REACH & OEKOTEX. Our Services Include: 1) Textile & Garment Testing 2) Gloves , Leather and Shoe Testing 3) Restricted Chemical – RSL Testing 4) Consumer Safety Testing 5) Petroleum and Petroleum By-Products Testing 6) Environmental Monitoring 7) Effluent Discharge Testing 8) Drinking Water Testing Tti is committed to deliver services as per the technical know-how with complete accuracy, at competitive prices. For this, we have the most modern testing facility in Pakistan equipped with state of the art testing equipment. All testing at Tti Testing laboratories is done on branded equipment with highly trained staff. Tti has helped reduce the inventory level of the work in process of the manufacturers’ by reducing lead-time required for testing. The rates we offer are the best possible in the world on branded state of the art equipment. w.ttilabs.net The accuracy and consistency of our work can be assessed by the fact that we at Tti have been participating in Proficiency Testing exercises conducted by ASTM and AATCC since 2003 onwards, which shows our performance in comparison to 70-80 laboratories worldwide. Furthermore, our Inspections division “Tti inspections Pvt Ltd” is one of the 5 Key ISO/IEC 17020 Accredited Inspection Bodies for Textiles- Textile Products operating in Pakistan. Services offered by Tti Inspection Pvt Ltd include: 1) Pre-production Inspection 2) During Production Inspection 3) Final Random Inspection 4) Supervision of Loading
National Accreditation Service Policy Launched
 
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Government has launched the National Accreditation Service policy to guide the establishment of the Country’s Accreditation Service agency that will give formal attestation that Conformity Assessment Bodies are competent to carry out specific conformity assessment activities. The policy guidelines paves way for an agency that will gain membership with the International Accreditation Forum and an associate member at the International Laboratory Accreditation Cooperation, the apex organizations on accreditation at a global level. Accreditation will be based on regional directives, relevant statutes and government regulations requirements for health, safety, and protection of the environment and market trends. Quality checkers such as the National Bureau of Standards, National Drug Authority and other related bodies will be subjected to the Accreditation Service Agency for attestation. The policy is in line with the government deliberate move to make domestically made services and products more competitive here and beyond. The lack of the National Accreditation Service Bureau is the reason for double quality checks on Uganda made products that already have certification with the Uganda quality bodies. And such means additional costs and low esteem for the domestically branded services and products hence low competitiveness.
Views: 75 NBS TV Uganda
Ghana Conformity Assessment Program - My Banner (1-10-14)
 
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Implementation of G-CAP suspended but traders and importers raise concerns.
Views: 154 MyJoyOnline TV