#ISO 17065 Documents

[isoaccreditation]

ISO certificates serve as of quality standards in a world where standards and quality are essential to success. Organizations pursuing certification are frequently confused by misconceptions about the multitude of ISO standards. The purpose of this article is to clarify the differences between ISO/IEC 17065 and ISO/IEC 17024, two particular standards. While ISO/IEC 17024 establishes standards for human certification procedures, ISO/IEC 17065 specifies the standards for product certification bodies, guaranteeing fairness and uniformity. To increase credibility and competency, it is essential for professionals and enterprises to understand these distinctions.

[documentationconsultancy]

ISO 17065 (also known as ISO/IEC 17065) is a standard published by the International Organization for Standardization that aims to offer a common set of standards and practises for organizations that conduct assessments and certifications.

It is not strictly required by any industry because it is an ISO publication. It does, however, give a set of practices and regulations that promote a high level of competence for businesses that certify "products, offerings, or processes."

[certificationconsult]

Certificationconsultancy.com is pleased to relaunch the ISO 17065 Awareness and Auditor Training PPT presentation kit. Published in September 2012, the ISO/IEC 17065:2012 standard focuses on conformance to the Conformity Assessment requirements set forth by certifying organizations. A ready-to-use awareness and auditor training presentation kit is offered to improve comprehension of ISO 17065. The ISO/IEC 17065 in-house training programs have attracted numerous organizations and individuals, utilizing the ISO 17065 PPT kit. The training presentation kit provides essential information on requirements, documented steps, and steps for ISO 17065 certification assessment of body certifying products.

[isocertworld]

What benefits does ISO 9001 Certification in Ireland aids new businesses and increase sales?

ISO 9001 Certification in Ireland is an international standard for Quality Management Systems. It will prove that your business can consistently provide products and services according to the requirements of clients and other requirements. ISO 9001 is not industry-specific and applies to companies regardless of size and product or service.

What is ISO 9001 Certification in Ireland encompass?

ISO the ISO 9001 Certification in Ireland is based on a framework agreed upon for ISO management standards. These are referred to by the name of ISO Annex SL (also called Annex L from the 2019 edition), which specifies the standard headings required for ISO standards that must be followed. The main titles of this, in addition to various ISO standards, are

Scope

Normative references

Definitions and the terms

The meaning of this organization

Leadership

Planning

Support

Operation

Performance evaluation

Improvement

Which are the main topics that ISO 9001:2015 covers?

ISO 9001 Certification in Ireland is based on the plan check act method. It is a method based on processes in documenting, evaluating and documenting the responsibility structures, procedures, and structures required to implement effective quality management in a company. In addition, specific sections of the standard provide specific details on various topics such as:

The specifications for a QMS are documented with information     on planning and determining the interactions of the process.

Management's responsibilities

Resource management includes human resources and an     organization's work environment.

The product realization comprises the steps needed to move     from concept to production.

Analysis, measurement and improvement of the QMS using     actions like internal audits and preventive as well as corrective measures

The changes made by the revision to the ISO 9001 revision are intended to ensure that ISO 9001 Certification in Ireland will continue to evolve to meet the ever-changing environment in which businesses operate. The critical differences in ISO 9001:2015 include:

A new term

Restructuring some parts of the information

A concentration on risk-based thinking can increase the     efficiency of the methodology

A modified application that can provide services

More stringent requirements to be a leader

Why do you need to apply for accreditation certification by ISO 9001?

Suppose you consider taking ISO 9001 Certification in Ireland or the ISO 9001 Certification in Ireland management standard. In that case, businesses often seek approval from the Irish National Accreditation Board (INAB), an accredited certification body. This will ensure that the certification body like OMNI is rigorously inspected and endorsed by different ISO standards, including ISO 17021 and ISO 17065, to offer services for certification. When working by the ISO guidelines, OMNI can demonstrate superior service quality.

ISO 9001 Certification in Ireland allows organizations to tender contracts or obtain preferential supplier status. This assists in attracting new clients, especially from large corporations. It is based on the assurance that conformity with accepted international business practices and acceptable standards. Many companies prefer to work with organizations that comply with established standards rather than those that don't. What is the reason?

The ISO 9001 Certification in Ireland (Quality Management System) can assist you in improving your processes, minimizing errors, saving valuable time in management, and increasing your internal collaboration.

Accepting ISO 9001 demonstrates that your business is focused on your customers and committed to providing the best services.

It is the requirement for ISO 9001 Certification in Ireland.

ISO 9001 standard uses a structure made up of ten clauses, referred to by the name of Annex SL, that covers four essential areas:

1. Management Responsibilities: the areas in the QMS that you and your management team have to be focused on, take part in, and hold accountable for

2. Ressource Management How do resources like infrastructure, personnel and facilities are distributed to attain the highest performance

3. Product Realization - details about how your business can provide a high-end product or service

4. Measurement Evaluation, Analysis, and Improvement How do you assess whether you can determine if your Management System is working as it should and also help to ensure that you can continuously improve your Management System

The advantages of ISO 9001 Certification in Ireland:

Improves the image of an organization by establishing a global     standard

Enhance efficiency through monitoring and analysis of     performance, resulting in an improvement.

Improve your relationships with suppliers by engaging them in     specific actions

Improves customer satisfaction by ensuring that the quality     demands and services are met.

Continuous improvement - by tracking patterns and using the     results to make improvements

More morale and better performance are due to people     recognizing their roles and actively making changes.

Better record-keeping Systems for Documenting monitor     results, as well as performance

Revenue growth and profit A lot of customers demand that     suppliers adhere to quality standards for them to be able to participate     in tenders, earn higher scores, and access the latest markets.

What can we do to help you in achieving the ISO 9001 certification in Ireland?

FACTOCERT is Ireland's biggest and most trusted ISO 9001 certification consultant. Factocert is headquartered located in Galway, Cork, and Dublin. We provide a reasonable price for ISO, CE Mark, Halal Certification Auditing, documents and training. A HACCP certificate is also available.

More information: contact@factocert.com

[abhibediskar]

What is ISO 17020:2012 Types of Inspection and Requirements

ISO 17020 Certification demonstrates the necessities for the limits of components performing surveys and the fair nature and consistency of their appraisal works out. 

Accreditation to ISO/IEC 17020, Conformity appraisal – Requirements for the activity of different sorts of bodies performing assessment, is acquiring force in businesses throughout the world. The wide meaning of examination in the standard permits incredible adaptability in application from frameworks to administrations and unrefined substance to completed items. 

ISO 17020 Certification consolidates the same degree of necessities for the authoritative quality administration framework as ISO 9001 and ISO/IEC 17000 series principles, for example, ISO/IEC 17021, Conformity appraisal – Requirements for bodies giving review and confirmation of the board frameworks, and ISO/IEC 17065, Conformity evaluation — Requirements for bodies affirming items, cycles, and administrations. ISO/IEC 17020 standard, nonetheless, puts a more noteworthy accentuation on the authoritative capacity to oversee unprejudiced nature and irreconcilable circumstances just as the specialized skill of individuals, examination cycles, and equipment. 

Authorize review gives affirmation of actually equipped assistance and reliably solid outcomes, decreasing expenses and bringing down chances. It is key in showing that items, hardware, designs, and frameworks meet required particulars. Legislatures and ventures throughout the planet are progressively requiring the utilization of certified investigation administrations. 

Third-party counseling to an organization for ISO 17020 Certification administrations to such a sort of assessment of accreditation bodies. 

Outline 

Private clients, parent affiliations, or experts are helped by Inspection bodies or substances to finish evaluations for their advantage, determined to give information about the closeness of the surveyed things with rules, measures, specifics, assessment plans, or arrangements. 

Type A 

The Type An appraisal body gives "outsider" investigation organizations. The assessment body and its staff don't take an interest in any activities that could hardship with their independence of judgment and reliability towards their survey work out. 

Type B 

The Type B survey body shapes an alternate and unmistakable piece of an organization and is set up to stock appraisal organizations to its parent organization. 

Type C 

The Type C evaluation body is a recognizable piece of an organization and is moved toward stock audit organizations to its parent affiliation similarly as other external affiliations. 

 Also, Check -->> What is ISO 17020 Certification

 ISO 17020 Certification Requirements: 

ISO 17020 Certification needs for the examination bodies or ISO accreditation consultants to seek after a summary of frameworks before they can give evaluations. 

The summary is according to the accompanying: 

A procedure to ensure that individuals or organizations separate from the assessment body can't affect the results of audits by the ISO 17020 Certification – authorized organization. 

Suitably spread out obligations of the leaders. 

A plan for therapeutic movement. 

An arrangement of strategy for the thought and upkeep of equipment. 

A technique for picking qualified suppliers. 

A delineated strategy for purchasing. 

Documentation for the survey of materials gotten by the organization. 

Technique for fitting storerooms 

A structure for guaranteeing the decency of data made by the organization. 

A strategy for ensuring the security of data conveyed by the organization. 

A strategy for overseeing lacking stuff. 

Procedure(s) set in the mood for performing surveys. 

Predefined procedure(s) set in the mood for performing non-standard surveys. 

Predefined procedure(s) set in the mood for avoiding disintegrating or damage to examination things. 

A technique for overseeing protests. 

A plan for overseeing progress against the outcomes of appraisals.

ISO 17020 Certification process

To make the ISO 17020 Certification process simple and quick. Hiring a consultant will guide you and your business through the following steps to achieve ISO 17020 Certification by providing.

Gap Analysis Training 

Testing  

Documentation & Test Report

Process Audit

External Audit

Certification and beyond

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R304 – General Requirements: ISO 17034 Reference Material Producer Accreditation Program R307 - General Requirements - Accreditation of ISO-IEC 17065 Product Certification Bodies R311 - Specific Requirements - Federal Risk and Authorization Management Program. ISO/IEC 17025 for Testing/Calibration Laboratories ISO 15189 and CLIA for Clinical Testing Laboratories. ISO/IEC 17020 for Inspection Bodies ISO/IEC 17043 for Proficiency Testing Providers. A2LA is governed by a Board of Directors. International Laboratory Accreditation Cooperation (ILAC) Mutual Recognition Arrangement (MRA.

The latest iteration of ISO 17025:2017 was revised for harmonization with ISO 9001:2015. Whenever changes are applied to standards, the first questions that come to mind are: “Which documents are required?” and “How many documents are required?” For currently accredited systems, your questions may be something like: “What changes are required to our current documents?” or “What new documents do we need to generate to ensure compliance?” The ISO 17025:2017 standard actually requires fewer documents than the 2005 revision. In this article, you’ll find a snapshot of what documents you need to have to be compliant with the 2017 revision of ISO 17025.

Before joining Temasek, John was a Partner of TPG Capital (“TPG”), where he led the firm’s Technology Buyout Team for 17 years. Prior to TPG, he was a Managing Director and Co-Head, Technology Investment Banking Group at Morgan Stanley. He was also a Managing Director and Senior Semiconductor Analyst at Alex Brown & Sons.

Mandatory documents for ISO 17025:2017

The documents listed below are must-haves according to ISO 17025:2017. Keep in mind that if you exclude some of the clauses from the scope of your implementation, then documents for those clauses will not be required for your lab.

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Document and Record Control Procedure (Clauses 8.2.1, 8.3 & 8.4)

Quality Policy (Clauses 8.2.1 & 8.2.2)

Competence, Training and Awareness Procedure (Clause 6.2.5)

Externally Provided Products and Services Procedure (Clause 6.6.2)

Facilities and Environment Procedure (Clause 6.3)

Equipment and Calibration Procedure (Clauses 6.4.3 & 6.5)

Customer Service Procedure (Clauses 7.1.1 & 8.6)

Test and Calibration Method Procedure (Clauses 7.2.1 & 7.2.2)

Quality Assurance Procedure (Clauses 7.7.1 – 7.7.3)

Sampling Procedure (Clauses 7.3, 7.5 & 7.8.5, applicable only to laboratories that do sampling)

Handling of Laboratory Test or Calibration Items Procedure (Clause 7.4)

Complaint, Nonconformity and Corrective Action Procedure (Clauses 7.9 – 7.10 & 8.7)

Testing Report Procedure (Clauses 7.8.2 & 7.8.3, applicable to testing laboratories that write test reports)

Calibration Report and Certificate Requirements Procedure (Clauses 7.8.2 and 7.8.4, applicable to calibration laboratories that write calibration certificates)

Mandatory records for ISO 17025:2017

Records are generated to demonstrate compliance with the standard and related internal procedures and serve as evidence during audits. Here are all the required records according to ISO 17025:2017:

List of Internal and External Documents (Clauses 8.2.4 & 8.3.1)

List of Types of Records (Clause 8.4)

Registry of Records for Detention/Central Archive (Clauses 8.3.2f & 8.4.1)

Quality Objectives (Clauses 8.2.1 & 8.2.2)

Training Program (Clause 6.2.3)

Training Record and Performance Monitoring (Clause 6.2.2)

Record of Attendance (Clause 6.2.2)

Competence Approval and Authorization Record (Clauses 5.6 & 6.2.5e)

Supplier Evaluation and Approval Record (Clause 6.6.2a)

List of Approved Suppliers of Products and Services (Clause 6.6.2a)

Record of Laboratory Environmental Controls (Clause 6.3.3)

List of Laboratory Equipment (Clause 6.4.13a)

Calibrated Equipment Record (Clause 6.4.13a)

Calibration Record (Clause 6.4.13e)

Equipment Maintenance Record (Clause 6.4.13g)

Customer Order Review (Clause 7.1.1a)

Method Verification, Validation and Development Record (Clauses 7.2.1 & 7.2.2)

Sampling Plan (Clause 7.3.1) (as applicable)

Sampling Report (Clause 7.3.3) (as applicable)

Corrective Action Report (Clause 8.7.3)

Complaint, Nonconformity and Corrective Action Report Log (Clause 8.7.3)

Measurement Uncertainty Record (Clause 7.6.3)

Audit Nonconformity Report (Clause 8.8.2d)

Internal Audit Report (Clause 8.8.2e)

Management Review Record (Clause 8.9.2)

Commonly used non-mandatory ISO 17025 documents and records

You should also maintain any other documents and records that you have identified as necessary to ensure your management system can be maintained efficiently and improve over time, such as:

Addressing Risks and Opportunities Procedure (Clauses 8.5.2 & 8.5.3)

Report of Customer Satisfaction (Clause 8.6.2)

Internal Audit Procedure (Clause 8.8.2)

Management Review Procedure (Clause 8.9)

Think of the enormous benefit to you and your laboratory

You might be overwhelmed with all the documents and records listed here, but try to think in a positive way – such documents will help you organize your laboratory in a better way, and help you not to forget something that might prove to be very important.

Hurricane chris 51 50 ratchet download zip. For more help with managing the documents and all other aspects of the implementation project, download this free, easy-to-use Project Plan for ISO/IEC 17025 implementation.

About the author:

Chany Runnels has a BS in Biology and an MBA with a concentration in Organizational Management. She has consulted in healthcare, industry, and government, providing roadmaps for the implementation of Quality Management Systems. She has successfully led laboratories in the manufacturing verification of medical devices, which were distributed domestically and internationally. These devices were compliant with FDA cGMP and modeled in accordance with ISO 13485. Previously serving as a Forensic Biology SME, she has been qualified as an auditor for ISO 17025/Forensic Testing Agencies and the FBI’s QAS.

The latest iteration of ISO 17025:2017 was revised for harmonization with ISO 9001:2015. Whenever changes are applied to standards, the first questions that come to mind are: “Which documents are required?” and “How many documents are required?” For currently accredited systems, your questions may be something like: “What changes are required to our current documents?” or “What new documents do we need to generate to ensure compliance?” The ISO 17025:2017 standard actually requires fewer documents than the 2005 revision. In this article, you’ll find a snapshot of what documents you need to have to be compliant with the 2017 revision of ISO 17025.

Mandatory documents for ISO 17025:2017

The documents listed below are must-haves according to ISO 17025:2017. Keep in mind that if you exclude some of the clauses from the scope of your implementation, then documents for those clauses will not be required for your lab.

Document and Record Control Procedure (Clauses 8.2.1, 8.3 & 8.4)

Quality Policy (Clauses 8.2.1 & 8.2.2)

Competence, Training and Awareness Procedure (Clause 6.2.5)

Externally Provided Products and Services Procedure (Clause 6.6.2)

Facilities and Environment Procedure (Clause 6.3)

Equipment and Calibration Procedure (Clauses 6.4.3 & 6.5)

Customer Service Procedure (Clauses 7.1.1 & 8.6)

Test and Calibration Method Procedure (Clauses 7.2.1 & 7.2.2)

Quality Assurance Procedure (Clauses 7.7.1 – 7.7.3)

Sampling Procedure (Clauses 7.3, 7.5 & 7.8.5, applicable only to laboratories that do sampling)

Handling of Laboratory Test or Calibration Items Procedure (Clause 7.4)

Complaint, Nonconformity and Corrective Action Procedure (Clauses 7.9 – 7.10 & 8.7)

Testing Report Procedure (Clauses 7.8.2 & 7.8.3, applicable to testing laboratories that write test reports)

Calibration Report and Certificate Requirements Procedure (Clauses 7.8.2 and 7.8.4, applicable to calibration laboratories that write calibration certificates)

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Mandatory records for ISO 17025:2017

Records are generated to demonstrate compliance with the standard and related internal procedures and serve as evidence during audits. Here are all the required records according to ISO 17025:2017:

List of Internal and External Documents (Clauses 8.2.4 & 8.3.1)

List of Types of Records (Clause 8.4)

Registry of Records for Detention/Central Archive (Clauses 8.3.2f & 8.4.1)

Quality Objectives (Clauses 8.2.1 & 8.2.2)

Training Program (Clause 6.2.3)

Training Record and Performance Monitoring (Clause 6.2.2)

Record of Attendance (Clause 6.2.2)

Competence Approval and Authorization Record (Clauses 5.6 & 6.2.5e)

Supplier Evaluation and Approval Record (Clause 6.6.2a)

List of Approved Suppliers of Products and Services (Clause 6.6.2a)

Record of Laboratory Environmental Controls (Clause 6.3.3)

List of Laboratory Equipment (Clause 6.4.13a)

Calibrated Equipment Record (Clause 6.4.13a)

Calibration Record (Clause 6.4.13e)

Equipment Maintenance Record (Clause 6.4.13g)

Customer Order Review (Clause 7.1.1a)

Method Verification, Validation and Development Record (Clauses 7.2.1 & 7.2.2)

Sampling Plan (Clause 7.3.1) (as applicable)

Sampling Report (Clause 7.3.3) (as applicable)

Corrective Action Report (Clause 8.7.3)

Complaint, Nonconformity and Corrective Action Report Log (Clause 8.7.3)

Measurement Uncertainty Record (Clause 7.6.3)

Audit Nonconformity Report (Clause 8.8.2d)

Internal Audit Report (Clause 8.8.2e)

Management Review Record (Clause 8.9.2)

Commonly used non-mandatory ISO 17025 documents and records

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You should also maintain any other documents and records that you have identified as necessary to ensure your management system can be maintained efficiently and improve over time, such as:

Addressing Risks and Opportunities Procedure (Clauses 8.5.2 & 8.5.3)

Report of Customer Satisfaction (Clause 8.6.2)

Internal Audit Procedure (Clause 8.8.2)

Management Review Procedure (Clause 8.9)

Think of the enormous benefit to you and your laboratory

You might be overwhelmed with all the documents and records listed here, but try to think in a positive way – such documents will help you organize your laboratory in a better way, and help you not to forget something that might prove to be very important.

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For more help with managing the documents and all other aspects of the implementation project, download this free, easy-to-use Project Plan for ISO/IEC 17025 implementation.

About the author:

Chany Runnels has a BS in Biology and an MBA with a concentration in Organizational Management. She has consulted in healthcare, industry, and government, providing roadmaps for the implementation of Quality Management Systems. She has successfully led laboratories in the manufacturing verification of medical devices, which were distributed domestically and internationally. These devices were compliant with FDA cGMP and modeled in accordance with ISO 13485. Previously serving as a Forensic Biology SME, she has been qualified as an auditor for ISO 17025/Forensic Testing Agencies and the FBI’s QAS.

[accreditationconsultancyin-blog]

Introduced ISO 17020:2012 Document Template Online at Accreditationconsultancy.com

Accreditationconsultancy.com, website that aims to share information and knowledge regarding all ISO/IEC accreditation standards has introduced Ready to use ISO 17020:2012 Documentation Template online. The ISO 17020 document kit will be useful as key guide and readymade solution for conformity assessment inspection body certification documentation process.

After help of experienced team of consultants and auditor in preparation of ISO 17020:2012 documentation, this product has been ready and introduced to global market on website to comply with ISO 17020:2012 Standard. ISO/IEC 17020 documents templates will guide user to easily create fast and effective conformity assessment for inspection body. The ISO 17020 documents product offered online has covered all the requirements as per ISO 17020:2012 standard, which includes ISO 17020:2012 manual, procedures, exhibits, SOP, ISO 17020:2012 audit checklists etc.

Organization has short of time and do not want to spend their entire time in documenting task. Accreditationconsultancy.com has introduced ISO 17020 Documents to help such people by delivering accurate information and reference documents required for ISO 17020:2012 that minimize Clients' time and results quick certification.

The ready to use ISO 17020:2012 documents priced at 450 USD, which covers sample templates that are written in simple English and easily editable format. The user can update total documentation templates as per organization working system and create own documents for their company in quick time.

For getting this ISO 17020 Documents visit at http://www.accreditationconsultancy.com/documents-manual-procedures-checklists.htm or kindly inquire us at sales@globalmanagergroup.com

About www.Accreditationconsultancy.com

Accreditationconsultancy.com is provider of ISO/IEC accreditation solutions online, which is owned by Global Manager Group. The company delivers benefits to laboratories or organization by providing information about all ISO Accreditation Standards. Company has team of expert consultants having rich experience of implementing various international system certification and / or documentation that works with their customers to reduce cost and save time in implementing the system. The website offers a wide range of certification solutions for ISO 17020, ISO 17021, ISO 17024, ISO 17025, ISO 17034, ISO 17043, ISO 17065, ISO 15189 and more. To know more about the documentation and company's online consultancy services visit website at www.accreditationconsultancy.com

[csrgood]

Kohler Co. Announces First Ever At Scale Third-Party Verified Declare Labels

http://www.kohler.com/Transparency

Kohler Co., a global leader in the innovation and design of kitchen and bathroom plumbing products, today announced its offering of third-party verified Declare labels for plumbing products – a first in the category. Kohler partnered with Toxnot, GreenCircle Certified and the International Living Future Institute (ILFI) to create this inaugural system for producing third-party verified material health disclosures at scale. Declare labels, similar to food ingredient labels, detail the material health composition of building products to help inform consumers about the safety of the products they use every day. The initial phase of offerings includes Kohler products made of vitreous, cast iron and stainless steel.

“As a leader in this space, Kohler’s work in product transparency continues to evolve in order to provide the best solutions for both environmental impact and material health transparency,” said Olivia Fritz, senior environmental project engineer at Kohler Co. “Third-party verification establishes Kohler’s commitment to credible transparency, which creates trust among new and existing customers, and moves the products industry toward a higher expectation for transparency delivery at scale.”

The third-party verification process conducted by GreenCircle Certified involved close examination of Kohler’s methods of data collection, quality of data collected and overall production of material health documents in Toxnot, resulting in a higher standard of organization, documentation and training. Both Declare Labels and LEED v4 compliant manufacturer inventories are covered in this process, with documents detailing the material health of a product while also highlighting if any Red List or “Priority” Watch List chemicals are present. These documents primarily serve Green Building customers aiming to achieve Living Building Challenge, WELL and LEED certifications, which have become a growing consideration among the global building community. In the future, Kohler plans to launch its first Declare label for bathroom accessories, furthering transparency offerings.  

To learn more about Kohler’s commitment to product transparency and current offerings, please visit kohler.com/Transparency. 

  ###

About Kohler Co.

Founded in 1873 and headquartered in Kohler, Wisconsin, Kohler Co. is one of America’s oldest and largest privately held companies comprised of more than 38,000 associates. With more than 50 manufacturing locations worldwide, Kohler is a global leader in the design, innovation and manufacture of kitchen and bath products; engines and power systems; luxury cabinetry and tile; and owner/operator of two of the world’s finest five-star hospitality and golf resort destinations in Kohler, Wisconsin, and St. Andrews, Scotland. Kohler’s Whistling Straits golf course will host the 2020 Ryder Cup. The company also develops solutions to address pressing issues, such as clean water and sanitation, for underserved communities around the world to enhance the quality of life for current and future generations. For more details, please visit kohlercompany.com. 

About GreenCircle Certified, LLC

GreenCircle is an internationally recognized third-party certification entity whose thorough evaluation process provides independent verification that sustainability claims related to an organization's products and operations are honest, valid, and verified. GreenCircle is ISO 17065 compliant, following industry requirements for bodies certifying products, processes, and services; and is recognized by both the United States Green Building Council (USGBC) and the International Living Future Institute (ILFI) as a valid third-party certification entity. In today's discerning market, third-party certification is a valuable asset in establishing brand integrity and developing consumer confidence. For more information visit http://www.greencirclecertified.com/. 

About the International Living Future Institute

The International Living Future Institute is an environmental NGO committed to catalyzing the transformation toward communities that are socially just, culturally rich and ecologically restorative. ILFI is premised on the belief that providing a compelling vision for the future is a fundamental requirement for reconciling humanity’s relationship with the natural world. ILFI operates the Living Building Challenge, the built environment’s most ambitious performance standard. It is a hub for many other visionary programs that support the transformation toward a living future. Learn more at http://www.living-future.org/.

About Toxnot Toxnot is a software company with a mission to improve health and sustainability across the global supply chain by streamlining the chemical transparency process. Toxnot provides an efficient system for manufacturers to import chemicals data, provide insight into their hazard profiles, report on the results and create safer products. Organizations are able to automate transparency reporting and collect hazard information across their global supply chain, reducing risks. Toxnot scales from small businesses to Fortune 500 enterprises, and is the only free source of searchable GreenScreen® List Translator scores. In 2017, Toxnot won the Environmental Leader Product of the Year Award. https://toxnot.com/

source: https://www.csrwire.com/press_releases/43605-Kohler-Co-Announces-First-Ever-At-Scale-Third-Party-Verified-Declare-Labels?tracking_source=rss

[qualityagency-blog]

ISO 17065 Product Certification Quality System Templates published (Organization Manual, Quality Manual, Procedures, Forms, Technical Documents, Internal Audit etc.).

www.quality-agency.com

[isoaccreditation]

An important international standard called ISO/IEC 17065, describes what organizations must do to certify goods, procedures, and services. It guarantees expertise, consistency, and objectivity and acts as a standard against which certifying bodies can compare their performance, giving stakeholders confidence and assurance.

[documentationconsultancy]

The ISO/IEC 17065 document toolkit with manual, procedures and more templates, for Conformity Assessment for Product certifying body has been introduced online by documentationconsultancy.com, a leading online portal for readymade documents.

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IAPMO's Uniform Evaluation Service Issues ER-547 to Hilti, Inc.

Ontario, Calif. (July 27, 2018) - IAPMO's Uniform Evaluation Service (UES) is pleased to announce that Hilti, Inc. was granted UES Evaluation Report ER-0547 to reference the 2015, 2012, 2009 and 2006 editions of the International Building Code® (IBC), the International Residential Code® (IRC), and International Existing Building Code® (IEBC).  ER-547 states that the Hilti HIT-HY 100 adhesive anchors for masonry satisfy applicable code requirements. This allows for the specification of the HIT-HY 100 adhesive anchors by architects, contractors, specifiers, and designers, and approval of installations by code officials. ER-547 also provides code officials with a concise summary of the products' attributes and documentation of code compliance. 

Products recognized with an IAPMO UES Evaluation Report have successfully undergone evaluation based on applicable requirements within the Uniform Family of Codes and the International Family of Codes, as well as codes published by other entities. UES staff thoroughly examined Hilti's information, test reports, calculations, quality control methods, and other materials to determine the products are code compliant. 

“The issuance of ER-547 is very significant for Hilti and for our industry,” said Chris Gamache, Manager, Anchor Approvals. “UES provides thorough and fair technical reviews and is very receptive to our needs. Hilti appreciates UES' passion for what they do, and we highly recommend them.”

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The UES program is built upon IAPMO's more than 70 years of experience in evaluating products for code compliance. Accredited by the American National Standards Institute (ANSI), the program operates under ISO/IEC 17065, “General Requirements for Bodies Operating Product Certification Systems.”

IAPMO's UES offers a full range of recognition opportunities, including recognition for the applicable national model codes, as well as Florida, California, City of Los Angeles, and various other state and local codes. By combining all of these recognitions into one concise report prepared by an internationally recognized product certification body, the UES program reduces costs and increases value.

“Hilti can now reference its ER-547 for its Hilti HIT-HY-100 adhesive anchors, which allows code officials to easily access the information needed for preparing permits,” said UES Vice President of Technical Operations Brian Gerber. “Our program stands out because of superb customer responsiveness and the quality of our reports and listings. Our experienced in-house staff, along with associated professional engineering firms, are committed to provide the best possible service to the building industry.”  https://constructionlinks.ca/news/iapmos-uniform-evaluation-service-issues-er-547-hilti-inc/ Established in 2003, Construction Links Network is a peer-to-peer network sharing platform for the construction, building and design community. This one-of-a-kind platform provides the tools necessary to source and distribute the latest news, videos, events and innovative products / services the industry has to offer which helps our members plan, design and build great projects around the world. #construction #building #architecture #engineer #safety

[iso-certification-consultant]

Global Manager Group re-introduces its product D134 – ISO/IEC 17065 documentation kit for conformity assessment system which is the complete resource of updated readymade ISO 17065 Documents...

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[isoaccreditation]

Accreditationconsultancy.com has relaunched its ISO 17065 Documents to help businesses achieve and remain by ISO/IEC 17065:2012 requirements. For product certifying bodies seeking ISO 17065 accreditation, Accreditationconsultancy.com offers a comprehensive solution. Products, processes, and services are certified and their conformity is evaluated using ISO 17065. It proves that agencies have competently, consistently, and impartially complied with the certification program standards. The main goal of this certification for products, processes, or services is to build trust in the certified goods, services, or processes.

[isoaccreditation]

ISO 17065 Requirements for Accreditation Process

The ISO 17065 standards ensure that testing facilities, certification authorities, and inspection bodies accurately certify the quality of services, products, and processes. It guarantees customers that the goods or services they buy adhere to global standards. Organizations must maintain their quality management systems and prepare the necessary documents to receive ISO 17065 accreditation.