http://finishedexams.com/homework_text.php?cat=2977
Immediate access to solutions for ENTIRE COURSES, FINAL EXAMS and HOMEWORKS “RATED A+" - Without Registration!
This document provides information about a Lead Auditor Course on FSSC 22000 (Food Safety) that is certified by IRCA. The course can be taken in a fast track 4 week format, regular weekday 6 week format, or weekend 8 week format. It is taught through instructor-led classroom training or live virtual training. The course objectives are to understand and apply the requirements of ISO 22000:2005, FSSC 22000, HACCP principles, and the roles of a lead auditor. Participants will learn auditing phases and techniques like report writing and follow-ups. A certificate of completion will be awarded to those who pass the assessment and exam.
QIC Inc.- Your Global Solutions PartnerTami Mulinix
QIC has a global network of industry consultants with offices in North America, Europe and Asia Pacific. Our diverse force of men and women has been serving our clients for more than 24 years. We are committed to quality, safety, and project accountability.
With our staff of engineers, technical managers, QA/QC specialists and administrative personnel, QIC offers a professional and experienced team to work with you on your project needs. With operations in many countries around the world, we have assembled a topnotch integrated workforce to ensure we meet our customers' needs.
This document provides information about API-U Q1 Practitioner Training, which teaches the requirements of the API Specification Q1 9th Edition quality management system. The training is intended for personnel involved in quality assurance, manufacturing, supplier evaluation, and specification of oilfield equipment. It will cover the documentation requirements and implementation process for the API Q1 quality system, as well as comparisons between the 8th and 9th editions. By the end of the course, participants will understand the API Q1 requirements and documentation, quality system development strategy, and certification process.
This document outlines the audit standards and types of audits conducted by two certification bodies - OJI Group Japan and Guardian Independent Certification Limited. Both conduct audits for ISO 9001, ISO 14001, and OHSAS 18001 management systems. The types of audits include stage 1 & 2 audits to evaluate implementation, surveillance audits to assess ongoing conformity, recertification audits to confirm continued effectiveness, and transfer audits when certifying from another body.
Karthick G is seeking a position as a Metrology Manager or in a related scientific/technical field. He has over 7 years of experience in testing and calibration of equipment according to ISO/IEC 17025 standards. He is proficient in inspecting and testing equipment at various levels and has experience maintaining calibrated equipment, conducting audits, and resolving customer complaints. He has helped acquire NABL accreditation for three companies and has demonstrated parameters in multiple audits.
Steve Isaac has over 20 years of experience in MRO and aerospace manufacturing. He currently works as Quality Assurance Manager for a plastics company that supplies aircraft components, where he helped them achieve EASA Part 145 and AS9100 certification. Isaac has extensive qualifications in quality auditing and aerospace standards including being an EASA Form 4 holder, AS9100 and ISO 9001 lead auditor, and Six Sigma Green Belt.
ISO17025 Accreditation Procedures and Process Abdul Rahman
A brief description of how to achieve ISO 17025 international accreditation. In this document, you would find how the organizations should react to fulfil the criteria of ISO-17025 and
Marty Evert has over 25 years of experience in quality management roles. He has a proven track record of improving quality systems and processes, reducing waste, and increasing supplier performance. Most recently as Quality Assurance Manager at ABW Technologies, he upgraded their quality management system, implemented new risk and configuration processes, and initiated supplier scorecards, reducing rework and waste. Previously as Quality Manager at B.E. Meyers Electro-Optics, revenues increased 40% after implementing their quality system, and they received top vendor ratings and status from Lockheed Martin.
This document provides information about a Lead Auditor Course on FSSC 22000 (Food Safety) that is certified by IRCA. The course can be taken in a fast track 4 week format, regular weekday 6 week format, or weekend 8 week format. It is taught through instructor-led classroom training or live virtual training. The course objectives are to understand and apply the requirements of ISO 22000:2005, FSSC 22000, HACCP principles, and the roles of a lead auditor. Participants will learn auditing phases and techniques like report writing and follow-ups. A certificate of completion will be awarded to those who pass the assessment and exam.
QIC Inc.- Your Global Solutions PartnerTami Mulinix
QIC has a global network of industry consultants with offices in North America, Europe and Asia Pacific. Our diverse force of men and women has been serving our clients for more than 24 years. We are committed to quality, safety, and project accountability.
With our staff of engineers, technical managers, QA/QC specialists and administrative personnel, QIC offers a professional and experienced team to work with you on your project needs. With operations in many countries around the world, we have assembled a topnotch integrated workforce to ensure we meet our customers' needs.
This document provides information about API-U Q1 Practitioner Training, which teaches the requirements of the API Specification Q1 9th Edition quality management system. The training is intended for personnel involved in quality assurance, manufacturing, supplier evaluation, and specification of oilfield equipment. It will cover the documentation requirements and implementation process for the API Q1 quality system, as well as comparisons between the 8th and 9th editions. By the end of the course, participants will understand the API Q1 requirements and documentation, quality system development strategy, and certification process.
This document outlines the audit standards and types of audits conducted by two certification bodies - OJI Group Japan and Guardian Independent Certification Limited. Both conduct audits for ISO 9001, ISO 14001, and OHSAS 18001 management systems. The types of audits include stage 1 & 2 audits to evaluate implementation, surveillance audits to assess ongoing conformity, recertification audits to confirm continued effectiveness, and transfer audits when certifying from another body.
Karthick G is seeking a position as a Metrology Manager or in a related scientific/technical field. He has over 7 years of experience in testing and calibration of equipment according to ISO/IEC 17025 standards. He is proficient in inspecting and testing equipment at various levels and has experience maintaining calibrated equipment, conducting audits, and resolving customer complaints. He has helped acquire NABL accreditation for three companies and has demonstrated parameters in multiple audits.
Steve Isaac has over 20 years of experience in MRO and aerospace manufacturing. He currently works as Quality Assurance Manager for a plastics company that supplies aircraft components, where he helped them achieve EASA Part 145 and AS9100 certification. Isaac has extensive qualifications in quality auditing and aerospace standards including being an EASA Form 4 holder, AS9100 and ISO 9001 lead auditor, and Six Sigma Green Belt.
ISO17025 Accreditation Procedures and Process Abdul Rahman
A brief description of how to achieve ISO 17025 international accreditation. In this document, you would find how the organizations should react to fulfil the criteria of ISO-17025 and
Marty Evert has over 25 years of experience in quality management roles. He has a proven track record of improving quality systems and processes, reducing waste, and increasing supplier performance. Most recently as Quality Assurance Manager at ABW Technologies, he upgraded their quality management system, implemented new risk and configuration processes, and initiated supplier scorecards, reducing rework and waste. Previously as Quality Manager at B.E. Meyers Electro-Optics, revenues increased 40% after implementing their quality system, and they received top vendor ratings and status from Lockheed Martin.
API Spec Q2 provides a new quality management standard for oil and gas service companies. It was created in response to business drivers like increasing well complexity, cost of non-productive time, and the need for consistent risk mitigation. Key aspects of API Spec Q2 include requirements for competency management, risk assessment, contingency planning, supplier controls, and validation of service quality. The standard is intended to improve reliability, minimize risks, and reduce non-productive time during well construction. It also promotes collaboration between service companies and operators to standardize quality expectations across the industry.
Marty Evert has over 25 years of experience in quality management roles. He has held positions at ABW Technologies, B.E. Meyers Electro-Optics, and VACI International. At his current and previous roles, he implemented quality management systems, improved supplier performance, and reduced waste. Marty holds a CMQ/OE certification from ASQ and certifications in ISO 9001, AS9100, auditing, and Six Sigma. He currently volunteers with the American Society for Quality.
A Timeline to Comply with ISO 13485:2016 (and what you need to be doing today)Greenlight Guru
To be blunt, if your company has put off doing anything about ISO 13485:2016, you need to act immediately.
We’re in the window where there is less than a year until you need to be ISO 13485:2016 certified. There is no extension. ISO won’t accept any excuses - this has been published for at least two years now.
This presentation covers:
- An overview of a timeline of activities you'll need to perform
- What happens if you don't get certified in time
- Best practices and a transition plan
- What auditors will be looking for in your stage 1 and stage 2 certification audits
- How to ensure all your quality processes are now "risk-based"
Watch the presentation here: https://www.greenlight.guru/webinar/iso-13485-2016-timeline
Effect of iso 9001 2015 on api q1 9th edJulián Rivera
The document provides a gap analysis between the requirements of ISO 9001:2015 and API Q1 9th Edition. It identifies 62 potential gaps in requirements between the two standards. The gaps are classified as unclear, clear but low impact, or clear but high impact. There are 9 unclear requirements, 31 low impact requirements, and 22 high impact requirements identified. The analysis indicates that while ISO 9001:2015 and API Q1 9th Edition specify similar quality management systems, there are some notable differences in specific requirements between the two standards.
The primary avenues for product approval with the Georgia Department of Transportation (GDOT) are the GDOT Qualified Products Lists (QPL) and the GDOT New Product Evaluation process. The QPL identifies products that have proven to meet GDOT specifications, while the New Product Evaluation process assesses new products for potential use. Other approval options include the National Transportation Product Evaluation Program (NTPEP) and the AASHTO Product Evaluation List (APEL), as well as GDOT task forces for specialized product categories.
The document discusses the upcoming API Q2 compliance standard for companies in the oil and gas industry. It notes that the deadline for compliance is quickly approaching in early 2014. It promotes a webinar that will help organizations understand how to use Intelex's EHSQ management software to proactively ensure they meet the new API Q2 standards, effectively manage changes, and evaluate their supply chain performance. The webinar covers how to reduce risks and move towards compliance through contingency planning and service quality plans.
The document provides information on ISO 9001:2008 quality management standards. It defines ISO 9001:2008 as an international standard that ensures a company has effective quality assurance systems in place to deliver quality products and services. It describes the key aspects of conforming to the standard, including having management establish quality policies and objectives, documenting procedures, implementing the quality system, and undergoing external audits to certify compliance. It also provides definitions of related terms like "quality management" and "quality assurance."
INSIGHTS IN CHEMICAL BIO-DECONTAMINATION: design, applications and validation...Fedegari Group
This workshop provides an overview of hydrogen peroxide technology for bio-decontamination. It will describe the process design, applications, and validation activities. Attendees will learn about Fedegari's hydrogen peroxide system through demonstrations and case studies. The training is intended for professionals in pharmaceutical and biotech industries using or considering hydrogen peroxide processes, including those in quality assurance, engineering, production, and microbiology. The one-day workshop will take place on January 26th, 2016 at the Fedegari Technology Center in Sellersville, Pennsylvania.
Marty Evert has over 30 years of experience in quality management roles. He has worked as a Quality Assurance Manager at ABW Technologies where he upgraded their quality management system to comply with AS9100 standards. Previously, he was the Quality Manager at B.E. Meyers where he led initiatives that increased revenues by 40% and improved supplier performance ratings. Evert also served as CEO of VACI International where he marketed and licensed patents in the automotive industry. He holds several quality management certifications.
The 10th annual World Quality Report found that 99% of respondents now use DevOps practices. The focus has shifted from whether to adopt DevOps to how to refine existing DevOps approaches. Customer satisfaction is now the top priority for QA and testing strategies. Challenges with test environments are hindering efficiency gains from trends like faster release cycles. Teams must acquire new skills like AI, IoT, and blockchain testing to keep up with technology changes. The report identified that the top test environment challenges are cost, defects from misconfiguration, lack of booking facilities, maintaining multiple versions, and visibility of untested areas.
ISO Training programs provided by TUV Soutwest - 2018.
Details are included for Awareness, Internal Auditor, Lead Auditor levels for following standards
1- ISO 9001:2015
2- ISO 14001:2015
3- ISO 45001:2018
4- ISO 22000:2018
5- ISO 27001:2013
6- ISO 20000-1:2012
7- ISO 22301:2012
8- ISO 55001:2014
9- ISO 50001:2018
10- ISO 31000:2018
11- ISO 21001:2018
12- ISO 17020:2012
13- ISO 17021-1:2015
14- ISO 17024:2012
15- ISO 17025:2017
16- ISO 17065:2012
Dynamic Strategies Iso Implementation Corporate Presentation Iidynamic67
The document provides information about Dynamic Strategies, an organization that offers management and process consulting services. It discusses Dynamic Strategies' vision, services, quality management system processes, and ISO 9001 certification requirements. Key points covered include Dynamic Strategies' commitment to quality and excellence, the services it offers related to process improvement, and explanations of quality management system concepts like documentation, audits, and process requirements.
Pedro Gonzalez has over 5 years of experience in quality assurance and inspection roles. He is currently a Quality Lead Inspector at Elbit Systems of America, where he performs inspections of military drones. Previously he was a Quality Lead at Adecco working at Celestica, where he led a team of 15 quality associates and performed failure analysis. He has a high school diploma and some college education.
The main differences and challenges between API Q2 and ISO 9001.
Set up in 1997, Environmental and Quality Solutions (EQS) specializes in helping companies streamline and maintain their management systems to achieve ISO standards of Quality, Health & Safety & Environmental Management.
ISO 13485 Lead Implementer - Four Page BrochurePECB
This training enables participants to develop expertise to implement and manage a Quality Management System based on ISO 13485. Over 5 days, participants will learn about QMS concepts, planning and initiating a QMS, implementing quality processes, controlling and measuring a QMS, and preparing for certification. The training aims to provide thorough understanding of ISO 13485 requirements and best practices for medical device quality management.
This document discusses establishing a European quality label and certification process to support eHealth interoperability. It proposes designing a harmonized process that operates with existing country-specific processes. This would benefit healthcare providers through a unified European market and ability to exchange data between regions and nations, and benefit industry through a single recognized European quality label and avoidance of duplicate testing. A functional model and case studies from France and the epSOS project are presented and guidelines are provided for deploying quality label and certification processes.
This document provides an overview of implementing an AS9100 quality management system. It discusses the benefits of implementing such a system, including helping win customers and improve internal processes. The document also describes the typical components of a quality management system, such as establishing documented processes, conducting internal audits, and continually improving processes based on audit findings. Finally, it outlines the 15 typical steps involved in implementing an AS9100 system, from planning and getting management support to achieving certification.
Curiosity and Infuse Consulting Present: Sustainable Test Automation Strategi...Curiosity Software Ireland
This webinar was co-hosted by Infuse Consulting and Curiosity Software on 27th September 2022. Watch the on demand recording here: https://opentestingplatform.curiositysoftware.ie/generate-rigorous-automated-tests-webinar
Your test automation rates are too low to match the speed of CI/CD, while suboptimal coverage is constantly letting bugs slip through. What do you do?
Many organisations treat this as a resourcing problem, often approaching services providers to navigate an automation skills shortage. Yet, hiring more people to perform the same processes is unsustainable, as the demand for automation persists sprint-over-sprint. In-house testing further risks growing dependent on a scripted framework that they can’t easily access or target for coverage. They risk throwing money constantly at external engineers to write repetitive scripts, fix brittle tests, and source test data. These suboptimal processes must be fixed first – people alone cannot fix test automation ROI.
This webinar will explore approaches to sustainable test automation that grows more efficient sprint-over-sprint, while targeting testing to de-risk the latest system changes. Nalin Parbhu, CEO of Infuse, and Curiosity’s George Blundell will draw on automation project experience from a range of different organisations. They will discuss collaborative approaches that automate processes surrounding test execution, while maximising reusability and optimising in-sprint test coverage. You will see solutions to perennial test automation barriers, including:
1. Collaborative test modelling, future proofing automation frameworks by maintaining intuitive living documentation.
2. In-sprint test and data generation, rapidly creating scripts from reusable flowchart models.
3. Automated test maintenance, targeting in-sprint coverage as requirements and systems change.
ISO/IEC 17025 General requirements for the competence of testing and calibration laboratories is the main ISO/IEC standard used by testing and calibration laboratories. In most countries, ISO/IEC 17025 is the standard for which most labs must hold accreditation in order to be deemed technically competent. In many cases, suppliers and regulatory authorities will not accept test or calibration results from a lab that is not accredited. Originally known as ISO/IEC Guide 25, ISO/IEC 17025 was initially issued by ISO/IEC in 1999. There are many commonalities with the ISO 9000 standard, but ISO/IEC 17025 is more specific in requirements for competence and applies directly to those organizations that produce testing and calibration results and is based on somewhat more technical principles. Laboratories use ISO/IEC 17025 to implement a quality system aimed at improving their ability to consistently produce valid results. It is also the basis for accreditation from an accreditation body.
The document provides an overview of a webinar presented by Omnex on VDA 6.3 Management. Omnex is an international consulting, training and software development organization that specializes in integrated management system solutions. The webinar covered VDA 6.3 process auditing standards including the audit process, product life cycle, and a review of sections P2 through P5 which relate to project management, planning product development, carrying out development, and supplier management.
Quality Standards & Business Excellence Models.pptNamyashah1
1. The document discusses various quality standards and business excellence models including ISO 9000, ISO 14001, and COPC 2000 Gold. It provides an overview of generic and industry-specific standards.
2. It describes certifications provided by ISO 9000 for organizations involved in different stages of production and services. Benefits of ISO 9000 certification include improved documentation, quality awareness, and operating standards.
3. Quality audits are classified as first party, second party, and third party audits. Nonconformances can be critical, major, or minor. Analytical tools like flowcharting and checklists can help auditors.
API Spec Q2 provides a new quality management standard for oil and gas service companies. It was created in response to business drivers like increasing well complexity, cost of non-productive time, and the need for consistent risk mitigation. Key aspects of API Spec Q2 include requirements for competency management, risk assessment, contingency planning, supplier controls, and validation of service quality. The standard is intended to improve reliability, minimize risks, and reduce non-productive time during well construction. It also promotes collaboration between service companies and operators to standardize quality expectations across the industry.
Marty Evert has over 25 years of experience in quality management roles. He has held positions at ABW Technologies, B.E. Meyers Electro-Optics, and VACI International. At his current and previous roles, he implemented quality management systems, improved supplier performance, and reduced waste. Marty holds a CMQ/OE certification from ASQ and certifications in ISO 9001, AS9100, auditing, and Six Sigma. He currently volunteers with the American Society for Quality.
A Timeline to Comply with ISO 13485:2016 (and what you need to be doing today)Greenlight Guru
To be blunt, if your company has put off doing anything about ISO 13485:2016, you need to act immediately.
We’re in the window where there is less than a year until you need to be ISO 13485:2016 certified. There is no extension. ISO won’t accept any excuses - this has been published for at least two years now.
This presentation covers:
- An overview of a timeline of activities you'll need to perform
- What happens if you don't get certified in time
- Best practices and a transition plan
- What auditors will be looking for in your stage 1 and stage 2 certification audits
- How to ensure all your quality processes are now "risk-based"
Watch the presentation here: https://www.greenlight.guru/webinar/iso-13485-2016-timeline
Effect of iso 9001 2015 on api q1 9th edJulián Rivera
The document provides a gap analysis between the requirements of ISO 9001:2015 and API Q1 9th Edition. It identifies 62 potential gaps in requirements between the two standards. The gaps are classified as unclear, clear but low impact, or clear but high impact. There are 9 unclear requirements, 31 low impact requirements, and 22 high impact requirements identified. The analysis indicates that while ISO 9001:2015 and API Q1 9th Edition specify similar quality management systems, there are some notable differences in specific requirements between the two standards.
The primary avenues for product approval with the Georgia Department of Transportation (GDOT) are the GDOT Qualified Products Lists (QPL) and the GDOT New Product Evaluation process. The QPL identifies products that have proven to meet GDOT specifications, while the New Product Evaluation process assesses new products for potential use. Other approval options include the National Transportation Product Evaluation Program (NTPEP) and the AASHTO Product Evaluation List (APEL), as well as GDOT task forces for specialized product categories.
The document discusses the upcoming API Q2 compliance standard for companies in the oil and gas industry. It notes that the deadline for compliance is quickly approaching in early 2014. It promotes a webinar that will help organizations understand how to use Intelex's EHSQ management software to proactively ensure they meet the new API Q2 standards, effectively manage changes, and evaluate their supply chain performance. The webinar covers how to reduce risks and move towards compliance through contingency planning and service quality plans.
The document provides information on ISO 9001:2008 quality management standards. It defines ISO 9001:2008 as an international standard that ensures a company has effective quality assurance systems in place to deliver quality products and services. It describes the key aspects of conforming to the standard, including having management establish quality policies and objectives, documenting procedures, implementing the quality system, and undergoing external audits to certify compliance. It also provides definitions of related terms like "quality management" and "quality assurance."
INSIGHTS IN CHEMICAL BIO-DECONTAMINATION: design, applications and validation...Fedegari Group
This workshop provides an overview of hydrogen peroxide technology for bio-decontamination. It will describe the process design, applications, and validation activities. Attendees will learn about Fedegari's hydrogen peroxide system through demonstrations and case studies. The training is intended for professionals in pharmaceutical and biotech industries using or considering hydrogen peroxide processes, including those in quality assurance, engineering, production, and microbiology. The one-day workshop will take place on January 26th, 2016 at the Fedegari Technology Center in Sellersville, Pennsylvania.
Marty Evert has over 30 years of experience in quality management roles. He has worked as a Quality Assurance Manager at ABW Technologies where he upgraded their quality management system to comply with AS9100 standards. Previously, he was the Quality Manager at B.E. Meyers where he led initiatives that increased revenues by 40% and improved supplier performance ratings. Evert also served as CEO of VACI International where he marketed and licensed patents in the automotive industry. He holds several quality management certifications.
The 10th annual World Quality Report found that 99% of respondents now use DevOps practices. The focus has shifted from whether to adopt DevOps to how to refine existing DevOps approaches. Customer satisfaction is now the top priority for QA and testing strategies. Challenges with test environments are hindering efficiency gains from trends like faster release cycles. Teams must acquire new skills like AI, IoT, and blockchain testing to keep up with technology changes. The report identified that the top test environment challenges are cost, defects from misconfiguration, lack of booking facilities, maintaining multiple versions, and visibility of untested areas.
ISO Training programs provided by TUV Soutwest - 2018.
Details are included for Awareness, Internal Auditor, Lead Auditor levels for following standards
1- ISO 9001:2015
2- ISO 14001:2015
3- ISO 45001:2018
4- ISO 22000:2018
5- ISO 27001:2013
6- ISO 20000-1:2012
7- ISO 22301:2012
8- ISO 55001:2014
9- ISO 50001:2018
10- ISO 31000:2018
11- ISO 21001:2018
12- ISO 17020:2012
13- ISO 17021-1:2015
14- ISO 17024:2012
15- ISO 17025:2017
16- ISO 17065:2012
Dynamic Strategies Iso Implementation Corporate Presentation Iidynamic67
The document provides information about Dynamic Strategies, an organization that offers management and process consulting services. It discusses Dynamic Strategies' vision, services, quality management system processes, and ISO 9001 certification requirements. Key points covered include Dynamic Strategies' commitment to quality and excellence, the services it offers related to process improvement, and explanations of quality management system concepts like documentation, audits, and process requirements.
Pedro Gonzalez has over 5 years of experience in quality assurance and inspection roles. He is currently a Quality Lead Inspector at Elbit Systems of America, where he performs inspections of military drones. Previously he was a Quality Lead at Adecco working at Celestica, where he led a team of 15 quality associates and performed failure analysis. He has a high school diploma and some college education.
The main differences and challenges between API Q2 and ISO 9001.
Set up in 1997, Environmental and Quality Solutions (EQS) specializes in helping companies streamline and maintain their management systems to achieve ISO standards of Quality, Health & Safety & Environmental Management.
ISO 13485 Lead Implementer - Four Page BrochurePECB
This training enables participants to develop expertise to implement and manage a Quality Management System based on ISO 13485. Over 5 days, participants will learn about QMS concepts, planning and initiating a QMS, implementing quality processes, controlling and measuring a QMS, and preparing for certification. The training aims to provide thorough understanding of ISO 13485 requirements and best practices for medical device quality management.
This document discusses establishing a European quality label and certification process to support eHealth interoperability. It proposes designing a harmonized process that operates with existing country-specific processes. This would benefit healthcare providers through a unified European market and ability to exchange data between regions and nations, and benefit industry through a single recognized European quality label and avoidance of duplicate testing. A functional model and case studies from France and the epSOS project are presented and guidelines are provided for deploying quality label and certification processes.
This document provides an overview of implementing an AS9100 quality management system. It discusses the benefits of implementing such a system, including helping win customers and improve internal processes. The document also describes the typical components of a quality management system, such as establishing documented processes, conducting internal audits, and continually improving processes based on audit findings. Finally, it outlines the 15 typical steps involved in implementing an AS9100 system, from planning and getting management support to achieving certification.
Curiosity and Infuse Consulting Present: Sustainable Test Automation Strategi...Curiosity Software Ireland
This webinar was co-hosted by Infuse Consulting and Curiosity Software on 27th September 2022. Watch the on demand recording here: https://opentestingplatform.curiositysoftware.ie/generate-rigorous-automated-tests-webinar
Your test automation rates are too low to match the speed of CI/CD, while suboptimal coverage is constantly letting bugs slip through. What do you do?
Many organisations treat this as a resourcing problem, often approaching services providers to navigate an automation skills shortage. Yet, hiring more people to perform the same processes is unsustainable, as the demand for automation persists sprint-over-sprint. In-house testing further risks growing dependent on a scripted framework that they can’t easily access or target for coverage. They risk throwing money constantly at external engineers to write repetitive scripts, fix brittle tests, and source test data. These suboptimal processes must be fixed first – people alone cannot fix test automation ROI.
This webinar will explore approaches to sustainable test automation that grows more efficient sprint-over-sprint, while targeting testing to de-risk the latest system changes. Nalin Parbhu, CEO of Infuse, and Curiosity’s George Blundell will draw on automation project experience from a range of different organisations. They will discuss collaborative approaches that automate processes surrounding test execution, while maximising reusability and optimising in-sprint test coverage. You will see solutions to perennial test automation barriers, including:
1. Collaborative test modelling, future proofing automation frameworks by maintaining intuitive living documentation.
2. In-sprint test and data generation, rapidly creating scripts from reusable flowchart models.
3. Automated test maintenance, targeting in-sprint coverage as requirements and systems change.
ISO/IEC 17025 General requirements for the competence of testing and calibration laboratories is the main ISO/IEC standard used by testing and calibration laboratories. In most countries, ISO/IEC 17025 is the standard for which most labs must hold accreditation in order to be deemed technically competent. In many cases, suppliers and regulatory authorities will not accept test or calibration results from a lab that is not accredited. Originally known as ISO/IEC Guide 25, ISO/IEC 17025 was initially issued by ISO/IEC in 1999. There are many commonalities with the ISO 9000 standard, but ISO/IEC 17025 is more specific in requirements for competence and applies directly to those organizations that produce testing and calibration results and is based on somewhat more technical principles. Laboratories use ISO/IEC 17025 to implement a quality system aimed at improving their ability to consistently produce valid results. It is also the basis for accreditation from an accreditation body.
The document provides an overview of a webinar presented by Omnex on VDA 6.3 Management. Omnex is an international consulting, training and software development organization that specializes in integrated management system solutions. The webinar covered VDA 6.3 process auditing standards including the audit process, product life cycle, and a review of sections P2 through P5 which relate to project management, planning product development, carrying out development, and supplier management.
Quality Standards & Business Excellence Models.pptNamyashah1
1. The document discusses various quality standards and business excellence models including ISO 9000, ISO 14001, and COPC 2000 Gold. It provides an overview of generic and industry-specific standards.
2. It describes certifications provided by ISO 9000 for organizations involved in different stages of production and services. Benefits of ISO 9000 certification include improved documentation, quality awareness, and operating standards.
3. Quality audits are classified as first party, second party, and third party audits. Nonconformances can be critical, major, or minor. Analytical tools like flowcharting and checklists can help auditors.
Quality Standards & Business Excellence Models.pptNamyashah1
1. The document discusses various quality standards and business excellence models including ISO 9000, ISO 14001, and COPC 2000 Gold. It provides an overview of generic and industry-specific standards.
2. Key certifications covered include ISO 9001, 9002, and 9003 which specify requirements for quality management systems for organizations involved in different stages of production and servicing.
3. Benefits of ISO 9000 certification identified in a survey include improved documentation, quality awareness, operating standards, and product quality perception.
ISO/IEC 17025 General requirements for the competence of testing and calibration laboratories is the main ISO/IEC standard used by testing and calibration laboratories. In most countries, ISO/IEC 17025 is the standard for which most labs must hold accreditation in order to be deemed technically competent. In many cases, suppliers and regulatory authorities will not accept test or calibration results from a lab that is not accredited. Originally known as ISO/IEC Guide 25, ISO/IEC 17025 was initially issued by ISO/IEC in 1999. There are many commonalities with the ISO 9000 standard, but ISO/IEC 17025 is more specific in requirements for competence and applies directly to those organizations that produce testing and calibration results and is based on somewhat more technical principles. Laboratories use ISO/IEC 17025 to implement a quality system aimed at improving their ability to consistently produce valid results. It is also the basis for accreditation from an accreditation body.
There have been three releases; in 1999, 2005 and 2017. The most significant changes between the 1999 and 2005 release were a greater emphasis on the responsibilities of senior management, explicit requirements for continual improvement of the management system itself, and communication with the customer. It also aligned more closely with the 2000 version of ISO 9001
The document discusses ISO 9000 standards for quality management systems. It provides an overview of ISO 9000, including its origins, organization, and key elements. The standards consist of requirements for quality management systems, including management responsibility, resource management, product realization, measurement, analysis and improvement. ISO 9000 certification involves developing and implementing a quality system, selecting a registrar, conducting self and third-party audits, and taking corrective actions.
The document summarizes a presentation by Chad Kymal on implementing ISO 9001:2000 in a way that increases value and reduces lead time. Kymal discusses common roadblocks in implementation and how to prevent them. He also outlines steps to transition from the 1994 standard, create value from the implementation, and drive culture change and savings quickly through a structured implementation plan and use of quality management software.
This document provides an overview and introduction to quality management systems and the ISO 9001:2015 and IATF 16949:2016 standards. It discusses key aspects of quality management including the basics of a QMS, requirements of the ISO and IATF standards, differences between the versions, transitioning processes, and implementing risk-based thinking. The document is intended to educate participants on quality management system requirements and certification.
Internal Audit Checklist__For ISO 9001_2015_.pdfNagarajPatil57
This document is an internal audit checklist for conducting a gap analysis of an organization's quality management system based on the requirements of ISO 9001:2015. It contains audit questions addressing each clause of ISO 9001:2015 to evaluate the organization's conformance and identify any gaps. The checklist outlines the audit plan, evaluation process, and templates for documenting gap analysis results and opportunities for improvement.
Awareness session on iatf 16949 2016 standardAmit Mishra
This document provides an agenda for training on IATF 16949. The training will cover an overview of IATF 16949 and how it relates to ISO 9001:2015. It will discuss the key changes between ISO/TS 16949:2009 and IATF 16949, including 14 specific changes. It will also cover the IATF structure, goals of IATF 16949, high level structure, notable changes in terminology, and clause-wise additions and explanations. The training will identify 17 documented processes required by IATF 16949 and certain frequency requirements.
The document provides an overview of IATF 16949:2016, the globally recognized quality management standard for the automotive industry. It discusses the history and evolution of the standard, from its origins in standards developed by major automakers in the 1990s to the current 2016 version. The key changes in IATF 16949:2016 include an emphasis on risk-based thinking, specific customer requirements, competence of auditors, product safety, manufacturer feasibility, and warranty management. The requirements of the standard are based on ISO 9001:2015's High Level Structure of 10 clauses and focus on continual improvement through a PDCA approach.
This document provides an overview of automotive quality management system audits as required by IATF 16949:2016, including:
- The types of audits that must be conducted, such as internal audits of the quality management system, manufacturing processes, and products.
- Requirements for planning, conducting, and documenting internal audits, as well as assessing supplier quality through second-party audits.
- Competency requirements for internal and second-party auditors, including necessary understanding of IATF 16949 and process-based auditing approaches.
- Key principles of conducting effective process-based audits, such as understanding the sequence and interaction of processes.
The ISO 9000 standard was created by European countries to promote quality and reduce waste. It provides guidelines for quality management systems that are now used by over 90 countries. Becoming ISO 9000 certified requires documenting processes, evaluating quality controls, and passing third-party audits. While certification requires work, many companies save money through increased efficiencies and see higher demand and sales by ensuring consistent product quality.
This document provides guidance for certification body auditors on conducting audits according to ISO/TS 16949. It outlines 31 required audit activities in a process flow chart and table. The table defines the knowledge and skills required of auditors for each activity, referencing source documents. It aims to ensure auditors are competent in areas that have been identified through IATF oversight of audits, such as having a process approach and knowledge of customer requirements and ISO/TS 16949.
Free and Open Source Software - Challenges for the Automotive Supply ChainShane Coughlan
The document discusses challenges that the automotive supply chain faces with open source software and how the OpenChain project provides solutions. OpenChain defines requirements for quality open source compliance programs and allows companies to self-certify or obtain third-party certification that they meet the requirements. This helps companies address licensing issues and predictably manage open source code in business-to-business contexts.
http://finishedexams.com/homework_text.php?cat=2973
Immediate access to solutions for ENTIRE COURSES, FINAL EXAMS and HOMEWORKS “RATED A+" - Without Registration!
The document provides information on defining a quality management system, including its key elements and purposes. A quality management system (QMS) can be defined as the organizational structure, procedures, processes and resources needed to implement quality management. The main elements of a QMS include organizational structure, responsibilities, methods, data management, processes, resources, customer satisfaction and continuous improvement. ISO 9000 standards provide requirements for QMS to help organizations ensure quality, efficiency and continual improvement.
INTERNATIONAL ORGANIZATION FOR STANDARDIZATION(ISO)waseemakhtar120
ISO 9000 and ISO 14000 are quality and environmental standards established by the International Organization for Standardization. ISO 9000 addresses quality management by specifying processes to fulfill customer requirements and regulatory compliance. ISO 14000 documents a firm's environmental program and specifies actions to minimize environmental impacts. Certification requires an external audit to ensure standards are met. Benefits of certification include competitive advantages, quality consistency, and improved environmental performance.
Walmart Business+ and Spark Good for Nonprofits.pdfTechSoup
"Learn about all the ways Walmart supports nonprofit organizations.
You will hear from Liz Willett, the Head of Nonprofits, and hear about what Walmart is doing to help nonprofits, including Walmart Business and Spark Good. Walmart Business+ is a new offer for nonprofits that offers discounts and also streamlines nonprofits order and expense tracking, saving time and money.
The webinar may also give some examples on how nonprofits can best leverage Walmart Business+.
The event will cover the following::
Walmart Business + (https://business.walmart.com/plus) is a new shopping experience for nonprofits, schools, and local business customers that connects an exclusive online shopping experience to stores. Benefits include free delivery and shipping, a 'Spend Analytics” feature, special discounts, deals and tax-exempt shopping.
Special TechSoup offer for a free 180 days membership, and up to $150 in discounts on eligible orders.
Spark Good (walmart.com/sparkgood) is a charitable platform that enables nonprofits to receive donations directly from customers and associates.
Answers about how you can do more with Walmart!"
Leveraging Generative AI to Drive Nonprofit InnovationTechSoup
In this webinar, participants learned how to utilize Generative AI to streamline operations and elevate member engagement. Amazon Web Service experts provided a customer specific use cases and dived into low/no-code tools that are quick and easy to deploy through Amazon Web Service (AWS.)
Chapter wise All Notes of First year Basic Civil Engineering.pptxDenish Jangid
Chapter wise All Notes of First year Basic Civil Engineering
Syllabus
Chapter-1
Introduction to objective, scope and outcome the subject
Chapter 2
Introduction: Scope and Specialization of Civil Engineering, Role of civil Engineer in Society, Impact of infrastructural development on economy of country.
Chapter 3
Surveying: Object Principles & Types of Surveying; Site Plans, Plans & Maps; Scales & Unit of different Measurements.
Linear Measurements: Instruments used. Linear Measurement by Tape, Ranging out Survey Lines and overcoming Obstructions; Measurements on sloping ground; Tape corrections, conventional symbols. Angular Measurements: Instruments used; Introduction to Compass Surveying, Bearings and Longitude & Latitude of a Line, Introduction to total station.
Levelling: Instrument used Object of levelling, Methods of levelling in brief, and Contour maps.
Chapter 4
Buildings: Selection of site for Buildings, Layout of Building Plan, Types of buildings, Plinth area, carpet area, floor space index, Introduction to building byelaws, concept of sun light & ventilation. Components of Buildings & their functions, Basic concept of R.C.C., Introduction to types of foundation
Chapter 5
Transportation: Introduction to Transportation Engineering; Traffic and Road Safety: Types and Characteristics of Various Modes of Transportation; Various Road Traffic Signs, Causes of Accidents and Road Safety Measures.
Chapter 6
Environmental Engineering: Environmental Pollution, Environmental Acts and Regulations, Functional Concepts of Ecology, Basics of Species, Biodiversity, Ecosystem, Hydrological Cycle; Chemical Cycles: Carbon, Nitrogen & Phosphorus; Energy Flow in Ecosystems.
Water Pollution: Water Quality standards, Introduction to Treatment & Disposal of Waste Water. Reuse and Saving of Water, Rain Water Harvesting. Solid Waste Management: Classification of Solid Waste, Collection, Transportation and Disposal of Solid. Recycling of Solid Waste: Energy Recovery, Sanitary Landfill, On-Site Sanitation. Air & Noise Pollution: Primary and Secondary air pollutants, Harmful effects of Air Pollution, Control of Air Pollution. . Noise Pollution Harmful Effects of noise pollution, control of noise pollution, Global warming & Climate Change, Ozone depletion, Greenhouse effect
Text Books:
1. Palancharmy, Basic Civil Engineering, McGraw Hill publishers.
2. Satheesh Gopi, Basic Civil Engineering, Pearson Publishers.
3. Ketki Rangwala Dalal, Essentials of Civil Engineering, Charotar Publishing House.
4. BCP, Surveying volume 1
বাংলাদেশের অর্থনৈতিক সমীক্ষা ২০২৪ [Bangladesh Economic Review 2024 Bangla.pdf] কম্পিউটার , ট্যাব ও স্মার্ট ফোন ভার্সন সহ সম্পূর্ণ বাংলা ই-বুক বা pdf বই " সুচিপত্র ...বুকমার্ক মেনু 🔖 ও হাইপার লিংক মেনু 📝👆 যুক্ত ..
আমাদের সবার জন্য খুব খুব গুরুত্বপূর্ণ একটি বই ..বিসিএস, ব্যাংক, ইউনিভার্সিটি ভর্তি ও যে কোন প্রতিযোগিতা মূলক পরীক্ষার জন্য এর খুব ইম্পরট্যান্ট একটি বিষয় ...তাছাড়া বাংলাদেশের সাম্প্রতিক যে কোন ডাটা বা তথ্য এই বইতে পাবেন ...
তাই একজন নাগরিক হিসাবে এই তথ্য গুলো আপনার জানা প্রয়োজন ...।
বিসিএস ও ব্যাংক এর লিখিত পরীক্ষা ...+এছাড়া মাধ্যমিক ও উচ্চমাধ্যমিকের স্টুডেন্টদের জন্য অনেক কাজে আসবে ...
How to Make a Field Mandatory in Odoo 17Celine George
In Odoo, making a field required can be done through both Python code and XML views. When you set the required attribute to True in Python code, it makes the field required across all views where it's used. Conversely, when you set the required attribute in XML views, it makes the field required only in the context of that particular view.
Reimagining Your Library Space: How to Increase the Vibes in Your Library No ...Diana Rendina
Librarians are leading the way in creating future-ready citizens – now we need to update our spaces to match. In this session, attendees will get inspiration for transforming their library spaces. You’ll learn how to survey students and patrons, create a focus group, and use design thinking to brainstorm ideas for your space. We’ll discuss budget friendly ways to change your space as well as how to find funding. No matter where you’re at, you’ll find ideas for reimagining your space in this session.
How to Setup Warehouse & Location in Odoo 17 InventoryCeline George
In this slide, we'll explore how to set up warehouses and locations in Odoo 17 Inventory. This will help us manage our stock effectively, track inventory levels, and streamline warehouse operations.
This presentation was provided by Steph Pollock of The American Psychological Association’s Journals Program, and Damita Snow, of The American Society of Civil Engineers (ASCE), for the initial session of NISO's 2024 Training Series "DEIA in the Scholarly Landscape." Session One: 'Setting Expectations: a DEIA Primer,' was held June 6, 2024.
1. OPS 571 Week 5 Quiz - New
buy here
http://finishedexams.com/homework_tex
t.php?cat=2977
www.finishedexams.com
Immediate access to
solutions
for ENTIRE COURSES,
FINAL EXAMS and
HOMEWORKS “RATED A+"
- Without Registration!
2. OPS 571 Week 5 Quiz - New
1)What is one analytical tool common to all quality improvement programs?
2)A fishbone diagram might be found in which DMAIC category?
3)What is the international quality management standard for quality management
and assurance that is primarily concerned with quality of air, water and soil?
4)What is a reason that a company may pursue ISO-9000 certification?
5)Who is responsible for performing the first-party certification audit for a
supplier firm?
6)What is the certification when a qualified national or international standards
body or similar certifying agency audits and certifies that a company is ISO
9000-complaint?
7)An opportunity flow diagram would best fit in which DMAIC category?
8)Which is the international standard for quality managements for automotive
industry suppliers of production parts, materials, and services?
9)ISO 9000 is primarily concerned with what type of quality management
standards?
10) What form of ISO 9000-certification is the final requirement before a
company may be registered and recorded as having achieved ISO 9000 status?