ISO 17025 certification gives testing and calibration laboratories the same type of accreditation that ISO 9001 gives to manufacturing and service organizations. Learn more at http://www.CEBOS.com
This document discusses the key requirements of ISO/IEC 17025 for testing and calibration laboratories. It covers management requirements, technical requirements, quality management systems, personnel requirements, accommodation and environmental conditions, test and calibration methods, equipment, measurement traceability, sampling, handling of test and calibration items, quality control, reporting of results, subcontracting, and opinions and interpretations. The main points are that ISO/IEC 17025 establishes the requirements for laboratories to demonstrate they are technically competent and able to produce valid results, laboratories must implement a quality management system, and personnel performing testing and calibrations must be qualified.
ISO/IEC 17025 outlines the requirements for laboratories to demonstrate competence and generate reliable test and calibration results. It covers management requirements like documentation, audits, and reviews as well as technical requirements for personnel, methods, equipment, measurement traceability and reporting. The standard requires laboratories to have a quality management system in place to ensure consistent, valid results and provide traceable measurements that can be compared internationally through an unbroken chain of calibrations.
The document outlines ISO 17025 requirements for management systems of testing and calibration laboratories. It discusses policies and procedures needed for contracts, subcontracting, suppliers, complaints, nonconforming work, corrective and preventive actions, internal audits, and management reviews. Laboratories must establish quality systems to ensure technical and management processes comply with ISO 17025 standards.
Estimation of Measurement Uncertainty in Labs: a requirement for ISO 17025 Ac...PECB
Â
Knowledge of the uncertainty of measurement of testing and calibration results is fundamentally important for laboratories, their clients and all institutions using these results for comparative purposes. Uncertainty of measurement is a very important metric of the quality of a result or a testing method.
Main points covered:
• To introduce the basic concepts related to measurement results and measurement uncertainty
• Explain the relevance of these concepts to chemical analysis data
• Introduce mathematical concepts, uncertainty sources and important approaches for estimation of measurement uncertainty
Presenter:
This webinar was presented by Dotun Bolade, who is an Analytical Chemist/Environmental Scientist by training and practice with years of experience in laboratory instrumentation and automation. For him, ISO management systems have become second nature having worked in environments where ISO 9001, 14001, 18001 and 17025 have been fully implemented. He is a Certified PECB ISO/IEC 17025 Lead Assessor.
Link of the recorded session published on YouTube: https://youtu.be/AOpFou7_FVI
Lakshy Management Consultant Pvt. Ltd. provides a 10 step approach to achieving ISO 17025 accreditation for testing and calibration laboratories. The 10 steps include awareness training, developing quality policies and objectives, gap analysis, documentation, implementation, internal audits, management reviews, pre-assessments, corrective actions, and the final accreditation audit. Lakshy assists clients through each step to ensure their organization meets all ISO 17025 requirements and receives accreditation.
The document provides a history of accreditation in the UK, beginning with the British Calibration Service established in 1966. It later merged with another organization to form the National Measurement Accreditation Service in 1985, which was renamed the UK Accreditation Service in 1995. The document also defines accreditation and certification, and explains that accreditation evaluates a laboratory's technical competence according to ISO/IEC 17025. It provides an overview of the requirements for laboratories to achieve and maintain accreditation.
This document discusses estimating uncertainties in experimental measurements. It explains that all measured values must include an estimated error or uncertainty. For a tennis ball measured to have a diameter of 6.4 cm, the estimated error is ±0.1 cm, meaning the actual diameter lies between 6.3-6.5 cm. There are two main types of errors: systematic errors associated with measurement devices or procedures, and random errors from fluctuating conditions. When adding or subtracting measured values, the numerical uncertainties are added. When multiplying or dividing, the percentage errors are added. Formulas are provided for calculating percentage error from numerical error. Examples demonstrate applying these rules to operations with measured values.
ISO 17025 certification gives testing and calibration laboratories the same type of accreditation that ISO 9001 gives to manufacturing and service organizations. Learn more at http://www.CEBOS.com
This document discusses the key requirements of ISO/IEC 17025 for testing and calibration laboratories. It covers management requirements, technical requirements, quality management systems, personnel requirements, accommodation and environmental conditions, test and calibration methods, equipment, measurement traceability, sampling, handling of test and calibration items, quality control, reporting of results, subcontracting, and opinions and interpretations. The main points are that ISO/IEC 17025 establishes the requirements for laboratories to demonstrate they are technically competent and able to produce valid results, laboratories must implement a quality management system, and personnel performing testing and calibrations must be qualified.
ISO/IEC 17025 outlines the requirements for laboratories to demonstrate competence and generate reliable test and calibration results. It covers management requirements like documentation, audits, and reviews as well as technical requirements for personnel, methods, equipment, measurement traceability and reporting. The standard requires laboratories to have a quality management system in place to ensure consistent, valid results and provide traceable measurements that can be compared internationally through an unbroken chain of calibrations.
The document outlines ISO 17025 requirements for management systems of testing and calibration laboratories. It discusses policies and procedures needed for contracts, subcontracting, suppliers, complaints, nonconforming work, corrective and preventive actions, internal audits, and management reviews. Laboratories must establish quality systems to ensure technical and management processes comply with ISO 17025 standards.
Estimation of Measurement Uncertainty in Labs: a requirement for ISO 17025 Ac...PECB
Â
Knowledge of the uncertainty of measurement of testing and calibration results is fundamentally important for laboratories, their clients and all institutions using these results for comparative purposes. Uncertainty of measurement is a very important metric of the quality of a result or a testing method.
Main points covered:
• To introduce the basic concepts related to measurement results and measurement uncertainty
• Explain the relevance of these concepts to chemical analysis data
• Introduce mathematical concepts, uncertainty sources and important approaches for estimation of measurement uncertainty
Presenter:
This webinar was presented by Dotun Bolade, who is an Analytical Chemist/Environmental Scientist by training and practice with years of experience in laboratory instrumentation and automation. For him, ISO management systems have become second nature having worked in environments where ISO 9001, 14001, 18001 and 17025 have been fully implemented. He is a Certified PECB ISO/IEC 17025 Lead Assessor.
Link of the recorded session published on YouTube: https://youtu.be/AOpFou7_FVI
Lakshy Management Consultant Pvt. Ltd. provides a 10 step approach to achieving ISO 17025 accreditation for testing and calibration laboratories. The 10 steps include awareness training, developing quality policies and objectives, gap analysis, documentation, implementation, internal audits, management reviews, pre-assessments, corrective actions, and the final accreditation audit. Lakshy assists clients through each step to ensure their organization meets all ISO 17025 requirements and receives accreditation.
The document provides a history of accreditation in the UK, beginning with the British Calibration Service established in 1966. It later merged with another organization to form the National Measurement Accreditation Service in 1985, which was renamed the UK Accreditation Service in 1995. The document also defines accreditation and certification, and explains that accreditation evaluates a laboratory's technical competence according to ISO/IEC 17025. It provides an overview of the requirements for laboratories to achieve and maintain accreditation.
This document discusses estimating uncertainties in experimental measurements. It explains that all measured values must include an estimated error or uncertainty. For a tennis ball measured to have a diameter of 6.4 cm, the estimated error is ±0.1 cm, meaning the actual diameter lies between 6.3-6.5 cm. There are two main types of errors: systematic errors associated with measurement devices or procedures, and random errors from fluctuating conditions. When adding or subtracting measured values, the numerical uncertainties are added. When multiplying or dividing, the percentage errors are added. Formulas are provided for calculating percentage error from numerical error. Examples demonstrate applying these rules to operations with measured values.
The document discusses the ISO/IEC 17025 standard for laboratory accreditation. It outlines the standard's requirements for management systems and technical operations. Specifically, it describes the standard's 15 management requirements and 10 technical requirements. It also explains the standard's requirements for quality management, document control, purchasing, corrective actions, internal auditing, and management reviews.
This document outlines the key requirements for document control within an ISO/IEC 17025 quality management system for testing and calibration laboratories. It discusses establishing procedures to control internal documents like manuals and procedures, as well as external documents like standards and regulations. Documents must be reviewed, approved by authorized personnel, and have a master list maintained with current revision status and distribution. Obsolete documents must be removed or marked as such. The document also provides guidance on document changes, document distribution, records retention, and archiving requirements.
This document discusses uncertainties and errors in physical measurements. It explains that there are two types of errors - random errors which are unpredictable, and systematic errors caused by imperfect measuring equipment. Random errors can be reduced by repeating measurements, while systematic errors are reduced by calibrating equipment. Accuracy refers to how close a measurement is to the true value, while precision refers to how close repeated measurements are. The number of significant figures reported in a result should not exceed the least precise value used. The document also discusses determining and expressing uncertainties in measurements, and how to combine uncertainties when performing calculations or graphing data.
Lima - Digital Forensic Case Management SystemIntaForensics
Â
The most effective Digital Forensic & E-Discovery Case Management System available commercially. "Best Buy" Award Winner in SC Magazine's Digital Forensic Tools Group Test 2013. Widely used in Law Enforcement, Commercial and Government Organisations in the USA, UK, EU, Canada & India
This document provides information about measurement and uncertainty in physics. It defines key terms like physical quantities, units, and order of magnitude. It discusses the International System of Units and its seven base units. The document also covers topics like derived units, significant figures, types of errors, calculating uncertainty, and basics of graphing collected data.
The Role of Proficiency Testing in Laboratory Quality AssurancePECB
Â
Proficiency Testing (PT), as it is introduced in ISO/IEC 17025, is the best method for evaluation of the laboratories performance by using interlaboratory comparisons. It provides independent evidence that the laboratory produces technically valid and reliable results. The techniques used in the statistical performance evaluation and how a round of proficiency testing is designed, implemented and evaluated will be described in this webinar.
Main points covered:
• Proficiency Testing (PT) as it is introduced in ISO/IEC 17025
• The techniques used in the statistical performance evaluation
• How a round of proficiency testing is designed, implemented and evaluated
Presenter:
This webinar was presented by Hamidreza Dehnad, PECB Certified Trainer and CEO of Pasargad Quality Pioneers (PQP).
Link of the recorded session published on YouTube: https://youtu.be/vp--EYDZq54
1) MIA Test Lab & Research Centre has received NABL approval to calibrate various linear instruments including external micrometers, height gauges, dial gauges, thickness gauges, plug gauges, and calipers.
2) The document provides the lab's contact information and price list for calibrating these instruments, with calibration charges ranging from Rs. 150 to Rs. 600 depending on the instrument type and range.
3) The lab requests that customers send their instruments for calibration or inform the lab so the instruments can be collected, and notes its terms and conditions including payment, delivery, and jurisdiction.
15. l'importance de l'iso cei 17025 pour l'infrastructure technique nationaleDavid Menezes
Â
ISO/IEC 17025 is an international standard that contains the requirements for a laboratory to be competent to carry out tests and/or calibrations. It helps ensure that laboratories produce precise and accurate test and calibration results. Accreditation to ISO/IEC 17025 provides formal recognition that a laboratory is competent. The standard contains both management system requirements and technical requirements related to personnel, accommodation, test and calibration methods, equipment, measurement traceability, sampling, handling of test items, and reporting of results. Compliance with ISO/IEC 17025 helps laboratories demonstrate technical competence and provides confidence in laboratory test and calibration results.
Complying with iso_17025_a_practical_guidebookHa Le
Â
This document provides a summary of a guidebook published by the United Nations Industrial Development Organization (UNIDO) titled "Complying with ISO 17025: A practical guidebook for meeting the requirements of laboratory accreditation schemes based on ISO 17025:2005 or equivalent national standards." The guidebook was written to assist testing and calibration laboratories in setting up a quality management system that conforms to ISO 17025:2005, the international standard for laboratory quality systems. Over its 16 chapters, the guidebook comprehensively covers all aspects of establishing systems and procedures to meet the requirements of ISO 17025. It provides specific, practical guidance for laboratories to evaluate their operations and identify areas of non-compliance in order to achieve accreditation
A corrective maintenance work order form to be used in executing maintenance in cases of breakdowns, emergencies and when an immediate action is required.
ISO 15189 Accreditation Guide - Improving Laboratory Performance Through Qual...Randox
Â
The document discusses ISO 15189 accreditation for medical laboratories. It outlines the importance of quality control and differences between accreditation and certification. Laboratories must implement both internal quality control and external quality assessment to gain ISO 15189 accreditation. This involves using third party controls, clinically relevant quality control material levels, peer group reporting, and participation in external quality assessment schemes. The document provides guidance on quality control considerations and processes needed to achieve and maintain ISO 15189 accreditation.
Proficiency Testing (PT) – a tool to improve laboratory performance - Brian B...Mara International
Â
The 3rd GCC Laboratory Proficiency Conference is organized as part of the strategic orientations of the GCC Standardization
Organization (GSO) for the development of the standardization and quality infrastructure, thereby contributing to the development of commerce and industry and to the support of national economy in the GCC member states.
Since the field of proficiency testing is newly introduced in the GCC member states and as the infrastructure of laboratories has not yet taken the shape of national or regional organizations representing the laboratories and reflecting their requirements, GSO is in need of meeting with a considerable group of laboratories to explore and prioritize GCC member states’ requirements in terms of the fields which must top the list of the fields to be developed and upgraded.
Based on the study conducted by GSO during 2011 on the status of proficiency testing activities in the member states which shown that the laboratories operating in the member states are in need of a unified data center on proficiency testing activities, GSO
organized two conferences in 2013 and 2014 on the subject. The conferences scored high rates of success in terms of the selected scientific material, quality of speakers and the targeted audience.
Accordingly, GSO conceptualization of the method of coordinating and upgrading the activity of proficiency tests in the GCC member states included a recommendation on the organization of annual training courses and awareness symposia by the GSO on the fields of proficiency tests.
This year’s Conference will be held in Dubai during two days the 24th and 25th of March 2015, and will coincide with the annual Analytical Industry exhibition ARABLAB which will be held in Dubai during the period 23 – 26 March 2015.
This document provides an overview of ISO 15189:2007, which establishes particular requirements for quality and competence in medical laboratories. It discusses the history and development of the standard, as well as key clauses related to organization, management, quality systems, personnel, equipment, pre-examination procedures, and more. The document is intended to train readers on the requirements of ISO 15189 through paraphrasing and rewording the standard.
This document discusses the requirements and process for laboratory accreditation according to ISO 15189 standards. It explains that accreditation is a formal recognition by an authoritative body that a laboratory is competent to perform specific tasks. The key requirements outlined include developing a quality management system, appointing a quality manager and technical manager, establishing quality indicators for monitoring and continual improvement, comprehensive documentation, and regular audits.
Determination of the potency of Paracetamol (Napa) tablet by UV-Spectrophoto...Protik Biswas
Â
This document describes an experiment to determine the potency of paracetamol tablets using UV spectrophotometry. Standard solutions of known paracetamol concentrations were prepared and their absorbances measured to generate a calibration curve. The absorbance of a sample tablet solution was then measured and used to calculate its concentration and potency. The calculated potency of 180.3% exceeded the specification range of 100% ± 10%, suggesting an experimental error occurred. Precautions are needed to properly handle equipment and solutions.
The document outlines the steps of a cyber forensic investigation process:
1. Verification and identification of systems involved to collect relevant data.
2. Preservation, collection and acquisition of evidence from systems in a manner that minimizes data loss and maintains a legally defensible chain of custody.
3. Processing, review and analysis of collected data through techniques like timeline analysis, keyword searching and data recovery to find relevant evidence.
This document is the quality manual for a laboratory. It begins by explaining the purpose and importance of having a quality manual according to ISO/IEC 17025 standards. The manual then outlines what should be included in the contents such as the quality policy statement, organizational structure, procedures, and documentation control. It provides details on the specific sections and documentation requirements for the management system, technical requirements, and quality control processes according to ISO standards. The quality manual is the key document that describes all aspects of the laboratory's quality management system.
Attribute control charts can be used to monitor processes where counts or percentages are recorded, using pass/fail criteria. There are four main types of attribute charts: p charts for non-conformity rates, np charts for non-conformity counts, c charts for defect counts, and u charts for defects per unit. Attribute charts indicate when a process is unstable and action needs to be taken by showing points outside the control limits. For example, a p chart showed an unstable process for writing purchase orders at a company due to defective orders, signaling the need for additional training.
Delhi is home to many skilled mehndi artists who create intricate designs on hands and feet. Mehndi application has been a wedding tradition in India for centuries as it is believed to bring good fortune. Artists in Delhi offer a wide variety of designs including Arabic, Punjabi, wedding, and Pakistani styles for special occasions. Common designs include Arabic motifs along with traditional Indian floral patterns for brides and simpler floral designs for unmarried women. Rajasthani mehndi uses extensive floral and leaf motifs in rangoli patterns up the arms and legs.
The document discusses the ISO/IEC 17025 standard for laboratory accreditation. It outlines the standard's requirements for management systems and technical operations. Specifically, it describes the standard's 15 management requirements and 10 technical requirements. It also explains the standard's requirements for quality management, document control, purchasing, corrective actions, internal auditing, and management reviews.
This document outlines the key requirements for document control within an ISO/IEC 17025 quality management system for testing and calibration laboratories. It discusses establishing procedures to control internal documents like manuals and procedures, as well as external documents like standards and regulations. Documents must be reviewed, approved by authorized personnel, and have a master list maintained with current revision status and distribution. Obsolete documents must be removed or marked as such. The document also provides guidance on document changes, document distribution, records retention, and archiving requirements.
This document discusses uncertainties and errors in physical measurements. It explains that there are two types of errors - random errors which are unpredictable, and systematic errors caused by imperfect measuring equipment. Random errors can be reduced by repeating measurements, while systematic errors are reduced by calibrating equipment. Accuracy refers to how close a measurement is to the true value, while precision refers to how close repeated measurements are. The number of significant figures reported in a result should not exceed the least precise value used. The document also discusses determining and expressing uncertainties in measurements, and how to combine uncertainties when performing calculations or graphing data.
Lima - Digital Forensic Case Management SystemIntaForensics
Â
The most effective Digital Forensic & E-Discovery Case Management System available commercially. "Best Buy" Award Winner in SC Magazine's Digital Forensic Tools Group Test 2013. Widely used in Law Enforcement, Commercial and Government Organisations in the USA, UK, EU, Canada & India
This document provides information about measurement and uncertainty in physics. It defines key terms like physical quantities, units, and order of magnitude. It discusses the International System of Units and its seven base units. The document also covers topics like derived units, significant figures, types of errors, calculating uncertainty, and basics of graphing collected data.
The Role of Proficiency Testing in Laboratory Quality AssurancePECB
Â
Proficiency Testing (PT), as it is introduced in ISO/IEC 17025, is the best method for evaluation of the laboratories performance by using interlaboratory comparisons. It provides independent evidence that the laboratory produces technically valid and reliable results. The techniques used in the statistical performance evaluation and how a round of proficiency testing is designed, implemented and evaluated will be described in this webinar.
Main points covered:
• Proficiency Testing (PT) as it is introduced in ISO/IEC 17025
• The techniques used in the statistical performance evaluation
• How a round of proficiency testing is designed, implemented and evaluated
Presenter:
This webinar was presented by Hamidreza Dehnad, PECB Certified Trainer and CEO of Pasargad Quality Pioneers (PQP).
Link of the recorded session published on YouTube: https://youtu.be/vp--EYDZq54
1) MIA Test Lab & Research Centre has received NABL approval to calibrate various linear instruments including external micrometers, height gauges, dial gauges, thickness gauges, plug gauges, and calipers.
2) The document provides the lab's contact information and price list for calibrating these instruments, with calibration charges ranging from Rs. 150 to Rs. 600 depending on the instrument type and range.
3) The lab requests that customers send their instruments for calibration or inform the lab so the instruments can be collected, and notes its terms and conditions including payment, delivery, and jurisdiction.
15. l'importance de l'iso cei 17025 pour l'infrastructure technique nationaleDavid Menezes
Â
ISO/IEC 17025 is an international standard that contains the requirements for a laboratory to be competent to carry out tests and/or calibrations. It helps ensure that laboratories produce precise and accurate test and calibration results. Accreditation to ISO/IEC 17025 provides formal recognition that a laboratory is competent. The standard contains both management system requirements and technical requirements related to personnel, accommodation, test and calibration methods, equipment, measurement traceability, sampling, handling of test items, and reporting of results. Compliance with ISO/IEC 17025 helps laboratories demonstrate technical competence and provides confidence in laboratory test and calibration results.
Complying with iso_17025_a_practical_guidebookHa Le
Â
This document provides a summary of a guidebook published by the United Nations Industrial Development Organization (UNIDO) titled "Complying with ISO 17025: A practical guidebook for meeting the requirements of laboratory accreditation schemes based on ISO 17025:2005 or equivalent national standards." The guidebook was written to assist testing and calibration laboratories in setting up a quality management system that conforms to ISO 17025:2005, the international standard for laboratory quality systems. Over its 16 chapters, the guidebook comprehensively covers all aspects of establishing systems and procedures to meet the requirements of ISO 17025. It provides specific, practical guidance for laboratories to evaluate their operations and identify areas of non-compliance in order to achieve accreditation
A corrective maintenance work order form to be used in executing maintenance in cases of breakdowns, emergencies and when an immediate action is required.
ISO 15189 Accreditation Guide - Improving Laboratory Performance Through Qual...Randox
Â
The document discusses ISO 15189 accreditation for medical laboratories. It outlines the importance of quality control and differences between accreditation and certification. Laboratories must implement both internal quality control and external quality assessment to gain ISO 15189 accreditation. This involves using third party controls, clinically relevant quality control material levels, peer group reporting, and participation in external quality assessment schemes. The document provides guidance on quality control considerations and processes needed to achieve and maintain ISO 15189 accreditation.
Proficiency Testing (PT) – a tool to improve laboratory performance - Brian B...Mara International
Â
The 3rd GCC Laboratory Proficiency Conference is organized as part of the strategic orientations of the GCC Standardization
Organization (GSO) for the development of the standardization and quality infrastructure, thereby contributing to the development of commerce and industry and to the support of national economy in the GCC member states.
Since the field of proficiency testing is newly introduced in the GCC member states and as the infrastructure of laboratories has not yet taken the shape of national or regional organizations representing the laboratories and reflecting their requirements, GSO is in need of meeting with a considerable group of laboratories to explore and prioritize GCC member states’ requirements in terms of the fields which must top the list of the fields to be developed and upgraded.
Based on the study conducted by GSO during 2011 on the status of proficiency testing activities in the member states which shown that the laboratories operating in the member states are in need of a unified data center on proficiency testing activities, GSO
organized two conferences in 2013 and 2014 on the subject. The conferences scored high rates of success in terms of the selected scientific material, quality of speakers and the targeted audience.
Accordingly, GSO conceptualization of the method of coordinating and upgrading the activity of proficiency tests in the GCC member states included a recommendation on the organization of annual training courses and awareness symposia by the GSO on the fields of proficiency tests.
This year’s Conference will be held in Dubai during two days the 24th and 25th of March 2015, and will coincide with the annual Analytical Industry exhibition ARABLAB which will be held in Dubai during the period 23 – 26 March 2015.
This document provides an overview of ISO 15189:2007, which establishes particular requirements for quality and competence in medical laboratories. It discusses the history and development of the standard, as well as key clauses related to organization, management, quality systems, personnel, equipment, pre-examination procedures, and more. The document is intended to train readers on the requirements of ISO 15189 through paraphrasing and rewording the standard.
This document discusses the requirements and process for laboratory accreditation according to ISO 15189 standards. It explains that accreditation is a formal recognition by an authoritative body that a laboratory is competent to perform specific tasks. The key requirements outlined include developing a quality management system, appointing a quality manager and technical manager, establishing quality indicators for monitoring and continual improvement, comprehensive documentation, and regular audits.
Determination of the potency of Paracetamol (Napa) tablet by UV-Spectrophoto...Protik Biswas
Â
This document describes an experiment to determine the potency of paracetamol tablets using UV spectrophotometry. Standard solutions of known paracetamol concentrations were prepared and their absorbances measured to generate a calibration curve. The absorbance of a sample tablet solution was then measured and used to calculate its concentration and potency. The calculated potency of 180.3% exceeded the specification range of 100% ± 10%, suggesting an experimental error occurred. Precautions are needed to properly handle equipment and solutions.
The document outlines the steps of a cyber forensic investigation process:
1. Verification and identification of systems involved to collect relevant data.
2. Preservation, collection and acquisition of evidence from systems in a manner that minimizes data loss and maintains a legally defensible chain of custody.
3. Processing, review and analysis of collected data through techniques like timeline analysis, keyword searching and data recovery to find relevant evidence.
This document is the quality manual for a laboratory. It begins by explaining the purpose and importance of having a quality manual according to ISO/IEC 17025 standards. The manual then outlines what should be included in the contents such as the quality policy statement, organizational structure, procedures, and documentation control. It provides details on the specific sections and documentation requirements for the management system, technical requirements, and quality control processes according to ISO standards. The quality manual is the key document that describes all aspects of the laboratory's quality management system.
Attribute control charts can be used to monitor processes where counts or percentages are recorded, using pass/fail criteria. There are four main types of attribute charts: p charts for non-conformity rates, np charts for non-conformity counts, c charts for defect counts, and u charts for defects per unit. Attribute charts indicate when a process is unstable and action needs to be taken by showing points outside the control limits. For example, a p chart showed an unstable process for writing purchase orders at a company due to defective orders, signaling the need for additional training.
Delhi is home to many skilled mehndi artists who create intricate designs on hands and feet. Mehndi application has been a wedding tradition in India for centuries as it is believed to bring good fortune. Artists in Delhi offer a wide variety of designs including Arabic, Punjabi, wedding, and Pakistani styles for special occasions. Common designs include Arabic motifs along with traditional Indian floral patterns for brides and simpler floral designs for unmarried women. Rajasthani mehndi uses extensive floral and leaf motifs in rangoli patterns up the arms and legs.
Ecommerce allows both small and large businesses to grow internationally with minimal investment and time. There are different types of ecommerce websites, including vanity websites like blogs, storefront websites that allow buyers and sellers to interact like online shopping sites, subscription websites that require payment to access content, and B2B websites that allow direct interaction between brands and customers. An ecommerce website designing company in Delhi can help businesses by eliminating geographical limitations, providing easy product navigation and accessibility on a single platform, and attracting customers with visibility in search engines while reducing costs.
Ecommerce allows both small and large businesses to grow internationally with minimal investment and time. There are different types of ecommerce websites, including vanity sites like blogs, storefront sites like online shopping malls, subscription sites requiring payment to access content, and B2B sites facilitating direct sales between brands and customers. An ecommerce website design company in Delhi can help businesses wipe out geographical limitations, provide easy product access and navigation, display detailed product information, attract customers through search engine visibility, and reduce costs.
The ISO guidelines document outlines the requirements for an organization's quality management system, including roles and responsibilities of personnel, scope of activities, documentation of testing procedures, reviews of contracts and services, purchasing, client services, complaints, and continual improvement. It also specifies validating testing and calibration procedures by documenting involved personnel, environmental conditions, equipment, measurement parameters, sample preparation methods, and report results to ensure quality and reliability.
ISO 17025 is an international standard for testing and calibration laboratories seeking accreditation. It has requirements for management, technical operations, and quality assurance. Accreditation increases confidence in test results, enhances customer satisfaction, and improves laboratory effectiveness through regular inspections. While accreditation requires costs for implementation and maintenance, it also provides benefits like reduced re-testing and an improved reputation. The standard has been adopted by accreditation bodies in several countries including Australia, New Zealand, and India.
ISO 17025 certification is an international standard that sets technical and management requirements for testing and calibration laboratories. There are two main segments - management prerequisites that address quality management systems, and technical prerequisites that check if tests and calibrations are accurate. Certification provides benefits like increased customer confidence, assurance in laboratory personnel and results, and listing in directories of accredited laboratories.
The ISO 14001 standard provides requirements for an environmental management system to help an organization develop and implement a policy and objectives that consider legal requirements and other requirements related to its significant environmental aspects. It applies to those environmental aspects that the organization determines it can control and impact. The standard does not require certification by an external organization but an organization may choose to be certified or seek confirmation of its environmental management system for various purposes such as customer assurance or regulatory compliance.
This document discusses the ISO 18001 standard for occupational health and safety management systems. ISO 18001 provides a framework for organizations to effectively manage health and safety in the workplace. Key benefits of implementing an ISO 18001 compliant system include minimizing risks to employees and contractors, compliance with legal requirements, and opportunities for cost savings through reduced accidents. The summary establishes the purpose and benefits of the ISO 18001 standard according to the document.
ISO 17025 standard establishes requirements for testing and calibration laboratories to demonstrate that they operate competently and generate valid results. The standard focuses on providing a systematic methodology for measuring the capability of staff in an organization to properly conduct objective tests assigned to them. It requires traceability and validation of test methods, implementation of a quality management system, and documentation of all measures taken and results obtained. Certification to this standard can increase an organization's objectivity, client satisfaction, opportunities for contracts, and ability to identify strengths, weaknesses, and areas for improvement.
ISO 9001 is an international quality management standard that aims to encourage global trade by providing a single standard recognized globally. It applies to organizations in many industries, including manufacturing, services, and more. The standard specifies requirements for a quality management system, including documented processes and procedures. Certification to ISO 9001 demonstrates that a company adheres to best practices for quality management and reduces risks for customers. It provides benefits such as improved process control, better documentation, a framework for improvements, and greater employee awareness of quality.
We are a leading website designing company offering professional and affordable website design and development services. With over 10 years of experience, our team of expert designers and developers can create fully responsive, user-friendly websites tailored to your business needs and goals. Some of our services include custom website design, e-commerce solutions, content management systems, and search engine optimization.
Main news related to the CCS TSI 2023 (2023/1695)Jakub Marek
Â
An English 🇬🇧 translation of a presentation to the speech I gave about the main changes brought by CCS TSI 2023 at the biggest Czech conference on Communications and signalling systems on Railways, which was held in Clarion Hotel Olomouc from 7th to 9th November 2023 (konferenceszt.cz). Attended by around 500 participants and 200 on-line followers.
The original Czech 🇨🇿 version of the presentation can be found here: https://www.slideshare.net/slideshow/hlavni-novinky-souvisejici-s-ccs-tsi-2023-2023-1695/269688092 .
The videorecording (in Czech) from the presentation is available here: https://youtu.be/WzjJWm4IyPk?si=SImb06tuXGb30BEH .
Have you ever been confused by the myriad of choices offered by AWS for hosting a website or an API?
Lambda, Elastic Beanstalk, Lightsail, Amplify, S3 (and more!) can each host websites + APIs. But which one should we choose?
Which one is cheapest? Which one is fastest? Which one will scale to meet our needs?
Join me in this session as we dive into each AWS hosting service to determine which one is best for your scenario and explain why!
Webinar: Designing a schema for a Data WarehouseFederico Razzoli
Â
Are you new to data warehouses (DWH)? Do you need to check whether your data warehouse follows the best practices for a good design? In both cases, this webinar is for you.
A data warehouse is a central relational database that contains all measurements about a business or an organisation. This data comes from a variety of heterogeneous data sources, which includes databases of any type that back the applications used by the company, data files exported by some applications, or APIs provided by internal or external services.
But designing a data warehouse correctly is a hard task, which requires gathering information about the business processes that need to be analysed in the first place. These processes must be translated into so-called star schemas, which means, denormalised databases where each table represents a dimension or facts.
We will discuss these topics:
- How to gather information about a business;
- Understanding dictionaries and how to identify business entities;
- Dimensions and facts;
- Setting a table granularity;
- Types of facts;
- Types of dimensions;
- Snowflakes and how to avoid them;
- Expanding existing dimensions and facts.
Let's Integrate MuleSoft RPA, COMPOSER, APM with AWS IDP along with Slackshyamraj55
Â
Discover the seamless integration of RPA (Robotic Process Automation), COMPOSER, and APM with AWS IDP enhanced with Slack notifications. Explore how these technologies converge to streamline workflows, optimize performance, and ensure secure access, all while leveraging the power of AWS IDP and real-time communication via Slack notifications.
TrustArc Webinar - 2024 Global Privacy SurveyTrustArc
Â
How does your privacy program stack up against your peers? What challenges are privacy teams tackling and prioritizing in 2024?
In the fifth annual Global Privacy Benchmarks Survey, we asked over 1,800 global privacy professionals and business executives to share their perspectives on the current state of privacy inside and outside of their organizations. This year’s report focused on emerging areas of importance for privacy and compliance professionals, including considerations and implications of Artificial Intelligence (AI) technologies, building brand trust, and different approaches for achieving higher privacy competence scores.
See how organizational priorities and strategic approaches to data security and privacy are evolving around the globe.
This webinar will review:
- The top 10 privacy insights from the fifth annual Global Privacy Benchmarks Survey
- The top challenges for privacy leaders, practitioners, and organizations in 2024
- Key themes to consider in developing and maintaining your privacy program
Salesforce Integration for Bonterra Impact Management (fka Social Solutions A...Jeffrey Haguewood
Â
Sidekick Solutions uses Bonterra Impact Management (fka Social Solutions Apricot) and automation solutions to integrate data for business workflows.
We believe integration and automation are essential to user experience and the promise of efficient work through technology. Automation is the critical ingredient to realizing that full vision. We develop integration products and services for Bonterra Case Management software to support the deployment of automations for a variety of use cases.
This video focuses on integration of Salesforce with Bonterra Impact Management.
Interested in deploying an integration with Salesforce for Bonterra Impact Management? Contact us at sales@sidekicksolutionsllc.com to discuss next steps.
HCL Notes and Domino License Cost Reduction in the World of DLAUpanagenda
Â
Webinar Recording: https://www.panagenda.com/webinars/hcl-notes-and-domino-license-cost-reduction-in-the-world-of-dlau/
The introduction of DLAU and the CCB & CCX licensing model caused quite a stir in the HCL community. As a Notes and Domino customer, you may have faced challenges with unexpected user counts and license costs. You probably have questions on how this new licensing approach works and how to benefit from it. Most importantly, you likely have budget constraints and want to save money where possible. Don’t worry, we can help with all of this!
We’ll show you how to fix common misconfigurations that cause higher-than-expected user counts, and how to identify accounts which you can deactivate to save money. There are also frequent patterns that can cause unnecessary cost, like using a person document instead of a mail-in for shared mailboxes. We’ll provide examples and solutions for those as well. And naturally we’ll explain the new licensing model.
Join HCL Ambassador Marc Thomas in this webinar with a special guest appearance from Franz Walder. It will give you the tools and know-how to stay on top of what is going on with Domino licensing. You will be able lower your cost through an optimized configuration and keep it low going forward.
These topics will be covered
- Reducing license cost by finding and fixing misconfigurations and superfluous accounts
- How do CCB and CCX licenses really work?
- Understanding the DLAU tool and how to best utilize it
- Tips for common problem areas, like team mailboxes, functional/test users, etc
- Practical examples and best practices to implement right away
AI 101: An Introduction to the Basics and Impact of Artificial IntelligenceIndexBug
Â
Imagine a world where machines not only perform tasks but also learn, adapt, and make decisions. This is the promise of Artificial Intelligence (AI), a technology that's not just enhancing our lives but revolutionizing entire industries.
Digital Marketing Trends in 2024 | Guide for Staying AheadWask
Â
https://www.wask.co/ebooks/digital-marketing-trends-in-2024
Feeling lost in the digital marketing whirlwind of 2024? Technology is changing, consumer habits are evolving, and staying ahead of the curve feels like a never-ending pursuit. This e-book is your compass. Dive into actionable insights to handle the complexities of modern marketing. From hyper-personalization to the power of user-generated content, learn how to build long-term relationships with your audience and unlock the secrets to success in the ever-shifting digital landscape.
In the rapidly evolving landscape of technologies, XML continues to play a vital role in structuring, storing, and transporting data across diverse systems. The recent advancements in artificial intelligence (AI) present new methodologies for enhancing XML development workflows, introducing efficiency, automation, and intelligent capabilities. This presentation will outline the scope and perspective of utilizing AI in XML development. The potential benefits and the possible pitfalls will be highlighted, providing a balanced view of the subject.
We will explore the capabilities of AI in understanding XML markup languages and autonomously creating structured XML content. Additionally, we will examine the capacity of AI to enrich plain text with appropriate XML markup. Practical examples and methodological guidelines will be provided to elucidate how AI can be effectively prompted to interpret and generate accurate XML markup.
Further emphasis will be placed on the role of AI in developing XSLT, or schemas such as XSD and Schematron. We will address the techniques and strategies adopted to create prompts for generating code, explaining code, or refactoring the code, and the results achieved.
The discussion will extend to how AI can be used to transform XML content. In particular, the focus will be on the use of AI XPath extension functions in XSLT, Schematron, Schematron Quick Fixes, or for XML content refactoring.
The presentation aims to deliver a comprehensive overview of AI usage in XML development, providing attendees with the necessary knowledge to make informed decisions. Whether you’re at the early stages of adopting AI or considering integrating it in advanced XML development, this presentation will cover all levels of expertise.
By highlighting the potential advantages and challenges of integrating AI with XML development tools and languages, the presentation seeks to inspire thoughtful conversation around the future of XML development. We’ll not only delve into the technical aspects of AI-powered XML development but also discuss practical implications and possible future directions.
GraphRAG for Life Science to increase LLM accuracyTomaz Bratanic
Â
GraphRAG for life science domain, where you retriever information from biomedical knowledge graphs using LLMs to increase the accuracy and performance of generated answers
How to Get CNIC Information System with Paksim Ga.pptxdanishmna97
Â
Pakdata Cf is a groundbreaking system designed to streamline and facilitate access to CNIC information. This innovative platform leverages advanced technology to provide users with efficient and secure access to their CNIC details.
Project Management Semester Long Project - Acuityjpupo2018
Â
Acuity is an innovative learning app designed to transform the way you engage with knowledge. Powered by AI technology, Acuity takes complex topics and distills them into concise, interactive summaries that are easy to read & understand. Whether you're exploring the depths of quantum mechanics or seeking insight into historical events, Acuity provides the key information you need without the burden of lengthy texts.
UiPath Test Automation using UiPath Test Suite series, part 6DianaGray10
Â
Welcome to UiPath Test Automation using UiPath Test Suite series part 6. In this session, we will cover Test Automation with generative AI and Open AI.
UiPath Test Automation with generative AI and Open AI webinar offers an in-depth exploration of leveraging cutting-edge technologies for test automation within the UiPath platform. Attendees will delve into the integration of generative AI, a test automation solution, with Open AI advanced natural language processing capabilities.
Throughout the session, participants will discover how this synergy empowers testers to automate repetitive tasks, enhance testing accuracy, and expedite the software testing life cycle. Topics covered include the seamless integration process, practical use cases, and the benefits of harnessing AI-driven automation for UiPath testing initiatives. By attending this webinar, testers, and automation professionals can gain valuable insights into harnessing the power of AI to optimize their test automation workflows within the UiPath ecosystem, ultimately driving efficiency and quality in software development processes.
What will you get from this session?
1. Insights into integrating generative AI.
2. Understanding how this integration enhances test automation within the UiPath platform
3. Practical demonstrations
4. Exploration of real-world use cases illustrating the benefits of AI-driven test automation for UiPath
Topics covered:
What is generative AI
Test Automation with generative AI and Open AI.
UiPath integration with generative AI
Speaker:
Deepak Rai, Automation Practice Lead, Boundaryless Group and UiPath MVP
Taking AI to the Next Level in Manufacturing.pdfssuserfac0301
Â
Read Taking AI to the Next Level in Manufacturing to gain insights on AI adoption in the manufacturing industry, such as:
1. How quickly AI is being implemented in manufacturing.
2. Which barriers stand in the way of AI adoption.
3. How data quality and governance form the backbone of AI.
4. Organizational processes and structures that may inhibit effective AI adoption.
6. Ideas and approaches to help build your organization's AI strategy.
2. INTRODUCTION
The ISO 17025 standard is implemented to ensure
competence and technical proficiency in the testing
laboratory. A research center that adopts a well secured
laboratory management system consistent with ISO
17025, means it has united with the world partnership of
licensed research facilities.
3. This accreditation will actually show your customers about
the value quality of your laboratory. And it will also help in
ensuring your customers that you are following all the
essential steps that are needed to deliver accurate and
reliable results. The ISO 17025 standard is available for all
types of laboratories, no matter whether they are
independent in nature or are part of any big enterprises.
Suppose you need to harden your research center's stance
as a genuine contender, then the very basic step is that
your research center management framework must comply
with the leading standards of the ISO 17025.
4. By having your lab administration structure licensed to ISO
17025, your organization can become proficient in
acquiring goldmine of profits. One of the principle points of
interest is that your lab will pick up global distinct image for
its responsibility to quality, competency and solid results.
Furthermore, this accreditation will imply that you are
agrede to a globally distinguished standard, thus moving
the worldwide trade of your company according to the best
market standard.
5. Best Advantages Of ISO 17025
Standard
• Universal Recognition
• Sound Management System
• Averts Defects
• Expanded Accuracy
• Cost Savings
• Diminished Waste
• Access to Global Marketplace
6. Reasons why you should go for such
accreditation services
• Accreditation is a great target approach to show your
clients that you have exhibited specialized ability to give
solid and exact test or adjustment fallouts.
• This type of assessment is also critical from the side of
the client, because it proves that your lab is performing at
its most elevated amount.
7. • An alternate profit of accomplishing ISO 17025
accreditation is that it will separate your lab from your
rivals. It is a perfect management system for research
centers as it serves the best medium for quality check.
• When the steps of this procedure executed rightly, the
constituents of ISO 17025 work precisely to guarantee
that all the levels are completely fulfilled. This could be an
effective strategic key.
8. This accreditation figure is answerable for all
the questions related to the quality
management system. And the specialized
parts of your framework confirm your
consistence to the prerequisites of ISO
17025 standard. It is the ultimate parameter
that at last decides whether your lab is
consenting to the standard or not.