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.

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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

Things that you should know about the ISO 17025:2017 Documentation for Various Laboratories

One such rule for ISO/IEC 17025 for that includes a list of ISO 17025:2017 requirements for testing laboratories. Testing laboratories need to be accredited to ISO/IEC 17025 to demonstrate their technical expertise and to ensure the accuracy of test results.

As we all know, ISO/IEC 17025 is one of the most important standards for all types of workplaces, universities and research institutes that perform experiments and calculations. ISO/IEC 17025 incorporates management and technical requirements that enable the testing or calibration laboratory to claim its technical competence. To have ISO 17025 accreditation by regulatory bodies proves that results are consistent and accurate and are produced using industry-standard standards.

Due to the use of unmaintained and uncalibrated instruments, Environment/Chemical Testing Laboratory factors, and to the skill level of the laboratory technician performing the tests are these variations. One reason for this variation is the production of potency reports to increase sales. This is usually done through the process of converting samples and test results.

The main purpose of any laboratory involved in analyzing the evaluation to obtain reliable results as possible, in a very short time. This means that regardless of the lab type, high quality and reliable analytical results. There is a need to efficiently manage resources such as personnel, test equipment and equipment, chemicals and reagents, laboratory environment and any other person involved in the production of results and data.

When you choose to provide laboratory testing or calibration, customer there may be a need to ensure that the supplier may issue relevant results. There are many aspects such as personnel competence, equipment reliability, validation and validation of testing methods, sample measurement procedures and calibration tracking at national and international standards that participate in laboratory technology.

So, For ISO/IEC 17025:2017 accreditation consultancy; Global Manager Group which has NABL 17025 Accredited Calibration lab provides facility Ready-to-Use ISO 17025 Documents to accreditation procedures in the calibration laboratory, Environment/Chemical Testing Laboratory as well as Civil Testing Laboratory across the globe. Also over 30 calibration laboratories globally are already accredited under guidance of GMG.

Based on good quality laboratory practices, Global Manager Group provides complete set of lab accreditation documentation kit with sample ISO 17025:2017 Manual, Quality Procedures, Exhibits, Work Instructions, and Sample Formats as well as ISO 17025:2017 Audit checklist for quick accreditation application for various such as Civil Material Testing Lab, Calibration Lab, Environmental Testing Lab, Chemical Testing Lab, Petroleum Testing Lab and Metal Testing Lab.

A global standard - ISO/IEC 17025 is for continuous improvement and maintenance. The laboratory complies with ISO/IEC 17025 benefits in the following ways:

• Improves the reliability of laboratory test results
• May develop technical capacity in case of consideration and/or legal issues
• The efficiency of lab increases , laboratory gains strong competitive advantage, and spending is reduced, customer complaints are reduced
• The Regulation facilitates tracking of ratings and calculations of good performance, sets the technical capacity of staff, maintains inspection equipment records, verifies the accuracy of test results, the accuracy and accuracy of test and calibration methods, the handling and flow of test materials, and the quality of the testing environment.

To get ISO 17025:2017 Consultancy for Accreditation for laboratories you can directly visit here - https://www.globalmanagergroup.com/Services/iso-17025-2017-consultancy-accreditation

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How should you choose best ISO/IEC 17020 Consultancy for Accreditation?

Thorough evaluation of a product (design and quality), service, process or plant is called "Inspection", which is also used to determine the conformity of an item in accordance with the requirements provided. ISO/IEC 17020:2012 is used to improve the quality and accuracy of Inspection Bodies.

Inspection Bodies Accreditation monitors the technical capabilities of the quality management system and provides guidelines for obtaining consistent and accurate inspection procedures.

Experts doing the test work are called inspectors and the general name "Inspection Bodies". The Inspection Bodies accreditation scheme provides formal recognition of the reliability and reliability of the testing body services. Proper implementation of ISO 17020 is critical to the complete maintenance of equipment, plant, tools, infrastructure, processes and the system itself.

The operations of various types of bodies performing inspection have been developed in order to build confidence in the inspection bodies are the requirements of ISO/IEC 17020 conformity assessment. The last version of ISO/IEC 17020 was published in year 1998. Since then, the 2012 version of ISO 17020 is in the implementation.

Mainly there are three major categories in which ISO 17020:2012 standard has categorized:

• Type-A: Inspection body, means an independent assessment body, which performs assessment tasks only,
• Type-B: Inspection body, means that its Inspection services will be provided only to the organization for which the test body is a component, and
• Type-C: Inspection body means that the Inspection body will provide security within the organization to ensure adequate separation of responsibilities and reporting between inspections and other activities.

Taking services of ISO 17020 consultancy for the implementation and ISO/IEC 17020:2012 certification for all types of inspection bodies, either on a temporary or long-term basis is very helpful in documentation, system implementation and getting accreditation or re-accreditation, as well as maintenance of the management system. But it is a very crucial to get a right consultancy such as any business partnership.

Such ISO 17020 consultancy provides following points can help you make the right selection:

• For each and every inspection parameter of the inspection bodies and preparation of detail Gap Analysis report and do Micro–level survey,
• Based on detailed study of all activities of the inspection bodies Preparation of applicable documents required by ISO/IEC 17020:2012, such as;
  1. ISO 17020 Quality Manual,
  2. Quality Procedures for ISO/IEC 17020:2012
  3. Standard Operating Procedures (SOPs) for inspection
  4. Formats to establish the objective evidence
• For maintaining and assuring quality of inspection services provided to its customer, Preparation of Quality Assurance Plan,
• Within the inspection bodies provide ISO 17020 training to all levels of employees,
• By periodic visit till accreditation, Help in effective implementation of system.
• To check readiness for the accreditation, Conduct internal audit for ISO 17020 system.
• In presence of Top Management, Conduct management review meeting to guide the inspection bodies for effective implementation of all the issues related to inspection,
• To build confidence among the employees, etc demonstrates the activities of inspection.

The ISO 17020 accreditation of inspection bodies need to have well-maintained ready-to-use ISO 17020 documents, which must contain ISO 17020:2012 Manual, iso 17020 procedures, formats, SOPs, audit checklist. So don’t waste time, choose a consultancy soon to conveniently achieve ISO 17020 Accreditation Certification in short time.

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ISO 17021 – What Mandatory Documents are required for ISO 17021 Accreditation for Certifying Body?

ISO/IEC 17021 is a standard developed for the evaluation of certification bodies to ensure they are qualified and compatible with all forms of management systems. A standards series of ISO 17021 is that set out requirements for organizations which provide certificates of conformity to all types of management systems. Accreditation bodies uses the ISO 17021 standards to evaluate the procedures that certification bodies have in place to make sure that they are impartial and the results of their assessments are consistent.

In actual, the original ISO/IEC 17021 was published in 2006. In the year 2015, a new version of ISO/ IEC 17021 is released. The norm helps guarantee certification bodies will be unbiased and compliant with their audit findings. According to this first release, two years from the first date of publication, approved IAF MLA management system certification bodies have been granted compliance with the standard.  In 2011, there was a revision that was focused on competence, and all certification bodies were given two years to conform to the new ISO 17021 standard.

For getting other international certifications, the ISO/IEC 17021 accreditation for certifying body requires standard documentation. And this Kind of standard documentation must conform to the Requirements of Conformity Assessment of certifying bodies as per ISO/IEC 17021:2015. The ISO 17021:2015 documents are globally used by certifying bodies and ISO 17021 consultants.  Such documents covers ISO/IEC 17021:2015 clause-wise requirements for quick ISO 17021 accreditation.

Following are the Mandatory ISO 17021 Documents which conforming to the conformity assessment requirements of Certifying Bodies as per ISO 17021:2015 is listed below:

• Sample ISO 17021 manual
• Quality Policy
• Procedures
• Standard Operating Procedures
• ISO 17021 Audit Checklist
• Sample Risk Templates
• Compliance Matrix

Accreditationconsultancy.com provides this kind of ISO 17021:2015 Documentation Kit for Certifying Body. One of the most significant features of this documentation kit is its user compatibility. An ISO 17021:2015 compliance matrix are requirements wise reference documents which also provided in the kit. So this kind of features makes easy for ISO 17021 consultants or any certifying body to establish linkage of standard requirements.

For worldwide recognition and credibility, An ISO 17021 accredited certification body has a definite edge over competitors. Here are the advantages of ISO/IEC 17021 accreditation include:

• Improvement of efficiency, productivity and effectiveness in the overall operation of certification
• Improvement in level of motivation, co-operation, and quality awareness including competence
• With the accreditation, Greater control of processes and activities throughout certification bodies
• The accreditation helps in analysis of data as well as perfect record-keeping
• It provides guidelines and better control for maintenance of records, etc.
• It establishes confidence of management and customers in the certificate  
• It increases customer trust as well as market shares
• The accreditation is helpful to make a better image as a quality certification body in global market

All details are of this sample ISO 17021:2015 documentation is in simple English, so there will be no difficulty in understanding the contents of this ISO 17021:2015 documentation kit. The certifying bodies or their ISO 17021 consultants can update sample document templates as per their working system and create own ISO 17021 documents for their company in only few days.

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What is Proficiency Testing & Why is it important?

With inter-laboratory comparisons, Proficiency testing (PT) is the evaluation of participant performance against pre-established criteria according to ISO/IEC 17043:2010 standard. Or we can say, a proficiency test is a method that used to demonstrate competency and validate a laboratory’s measurement process by comparing results to the results of a participant laboratories and other reference laboratories.

A coordinating body sends a test item or in other words reminder to a reference laboratory for testing. Each participant laboratory will test the item independently, submit their results to the coordinating body, and forward the item to the next participating laboratory. The item is returned to the coordinating body after each participating laboratory has completed testing. To each participating laboratory, the coordinating body will evaluate the all the test results and issue a performance report.

Importance of Proficiency Testing

For Several reasons Proficiency Testing is important. Basically, it enables your laboratory to demonstrate competency for a particular measurement discipline which can be used to validate;

• A measurement method;
• Technical training of personnel;
• Traceability of standards, and
• Estimates of measurement uncertainty.

Imagine that A new measurement or testing capability to your scope of accreditation is added that your laboratory. Even with all of that hard work, times, and money invested into your new process. Your laboratory can externally validate your new measurement or testing process with participating in proficiency testing. Hence, the reason accreditation body requires you to successfully complete a proficiency test before they will add it to your scope of accreditation.

One of the proficiency test providers - ISO 17043:2010 Accreditation Consultancy is assisting with system implementation, preparation of ISO 17043 documents, including ISO 17043 manual, as well as conducting training programs on system awareness and training of auditors; The team of experienced ISO 17043 accreditation consultants offers guidance on ISO 17043 accreditation and documentation.

Behind the goal of editable ISO 17043 Documents is to support proficiency test provider in ISO 17043:2010 documentation and give confidence to their customers, regulating authorities and accreditation bodies, As well as ISO 17043 consultants that meet all documentation requirements. Accreditationconsultancy.com provides services which are helpful for proficiency test provider to achieve ISO 17043:2010 accreditation in minimum time and cost.

You could possibly require (both mandatory and optional) every document template for ISO 17043, as well as additional work instructions, project tools and documentation structure guidance, the really is the most comprehensive option - ISO 17043 Documentation Toolkit on the market for completing your documentation.

Advantages of ISO 17043 documents for proficiency test provider’s accreditation

• Easily modifiable templates according to your requirements.
• For establishing good ISO 17043 system, Helps in fine-tuning the processes. 
• To prepare any document that saves much time and cost.
• Minimizes excessive paperwork.
• To determine the baseline system of ISO 17043 that satisfies requirements for personnel certification body as well as covers its principles.

Introduction to ISO 17043 Accreditation requirements

To consider conformity assessment, the ISO Committee on conformity assessment (CASCO) is responsible for the development of International Standards and Guides. ISO 17043 standard was developed by ISO committee on conformity assessment.

The ISO/IEC 17043:2010 accreditation specifies requirements of conformity assessment for proficiency testing. ISO 17043 Accreditation for proficiency test providers makes sure those customers of compliance with international standards and good practices. With ISO 17043 Accreditation, proficiency test providers gain increased confidence that the programs that depends on are being operated competently in accordance with the specified technical and management system requirements.

Proficiency testing is the one of mechanisms through which the performance of an organization can be checked to confirm its ability to stick to the organization’s procedures. Proficiency testing (PT) is a current requirement of accreditation programs offered by International Laboratory Accreditation Cooperation Mutual Recognition Arrangement signatory accreditation bodies and is a common requirement of regulatory and oversight programs. Proficiency testing is a quality control tool that can be utilized prior to achieving accreditation.

ISO 17043:2010 Accreditation demands technical competence assurance and good quality management practices, but also includes verification of the proficiency test management of the provider. ISO/IEC 17043:2010 recognizes proficiency testing as a participant performance as well as evaluation against pre-established criteria which is meaning of interlaboratory comparisons for the determination of laboratory performance.

Following are ISO/IEC 17043, Conformity assessment — General requirements for proficiency testing,

• Personnel
• Design of proficiency testing schemes
• Preparation of proficiency testing items
• Assigned values 
• Data analysis and proficiency testing evaluation scheme results
• Data analysis and their records
• Reports 

ISO/IEC 17043 states purpose of Proficiency testing,

1. Performance of laboratories evaluation for specific tests or measurements and monitoring laboratories' continuing performance;
2. Problems in laboratories of identification and initiation of actions for improvement, 
3. Establishment of the effectiveness of test and compare to them ;  
4. Inter-laboratory differences identification;  
5. Education of participating laboratories based on the outcomes of such comparisons;
6. Validation of uncertainty claims .

Proficiency testing programs exist in different formats. As well as in the most comprehensive form, proficiency testing involves three distinct entities: the participant of proficiency provider, the proficiency test provider, and the bodies that accredit the proficiency test providers. Anyways, the roles of each entity may overlap.

The accreditation programs require that the proficiency test user’s results are reported within the participant’s quality assurance system.

Different forms of Proficiency tests:

• Accrediting bodies may facilitate a proficiency test. 
• Users may create and administrate a proficiency test to internal and external users 
• Users may evaluate proficiency through alternatives such as observation or case presentation
• Proficiency tests may be purchased and results reported externally. 
• Proficiency tests may be created or purchased externally. 
• Proficiency tests results may be reported internally.

ISO 15189 Check List and Requirement

ISO 15189 pens down the requirements for quality and competence in medical laboratories. This international standard is used by medical laboratories in developing their quality management systems and assessing their own competence.

This standard is essential for the company’s goodwill as it is used for confirming or recognizing the competence of medical laboratories by laboratory customers, regulating authorities and other accreditation bodies.

ISO 15189 Check List:

Based on ISO 17025 and ISO 9001 few additional requirements are laid down in ISO 15189. Such as-

•    Providing advice on the type of sample and testing that are required.

•    Having an interaction with clinical staff responsible for the quality of service to clinicians.

•    Providing opinions on the results of testing.

•    Collecting samples or suggesting information on collection procedures, sample containers, and sample volumes.

•    To check whether they are working as per ethics.

ISO 15189 accreditation involves an independent assessment of the medical laboratory that includes an examination of personnel qualifications and competence, equipment, reagents and supplies, quality assurance, and analytical, pre-analytical, and post-analytical factors.

Qualified auditors conduct a thorough evaluation of all factors affecting the production of test data. To ensures the quality regular checkups are conducted.

Accreditation consultancy is one of the premier documents selling companies and is serving national and international markets with full dedication since ages.

We are engaged in providing consultancy services and training on ISO 15189 Certification. Known for serving customers with all the best efforts, we assure you on every step about your ISO 15189 certification.

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