Whether you're looking for your first calibration management program or looking to upgrade from a current system, you'll find that Labsols CALIBRATION LIMS has everything you need.
1. Manage Calibration Process and Operation flow
2. Manage Sales Process (Sales Order to Shipment to Billing)
3. Manage Lab Standards/Master Products
4. Manage Lab Staff workload and lab performance
5. Manage Calibration documents and communication
6. Manage Lab Customers and connected to them all time
Completely customized to your current business and lab operations (sales order, batch calibrations, sampling, result entry, multiple-bespoke reports, shipment, billing, document management, KPI, and more)
Comes with Intelligent integration of calibration customer facing portal and mobile apps.
An overview of ASQ Quality Auditor (CQA) certification program with tips for passing exam
http://seetharamkandarpa.webnode.in/news/web-series-session-1-overview-of-asq-certified-quality-auditor-conducted-on-21-may-2017/
This presentation gives a bried overview of the various parts & purpose of the ISO 9001:2015 QMS.
It revolves around the PDCA Cycle and useful in Manufacture & construction Industry.
The most valuable Helpful PDF file that extremely can boost your ability to understand well the New version of QMS in accordance to ISO 9001:2015 as well as ease the documentation transition process toward ISO 9001:2015
The document provides an overview of the ISO 9001 quality management standard and certification process. It discusses the key principles and requirements of ISO 9001, including customer focus, leadership, engagement of people, process approach, and continual improvement. It also outlines the certification requirements and critical success factors for organizations going through the ISO 9001 implementation and certification process.
The document outlines a 10 step approach used by Lakshy Management Consultant Pvt. Ltd. to implement ISO 9001 certification. The 10 steps include awareness training, developing a quality policy and objectives, gap analysis, documentation and process design, implementation, internal audits, management reviews, shadow audits, corrective actions, and the final certification audit. Lakshy provides consulting services to guide clients through each step of the ISO 9001 implementation and certification process.
This document provides information about an ISO 9001:2008 Lead Auditor training course, including details about the course content, assessment, delivery style, and auditor requirements. The course covers quality management principles, ISO standards, auditing planning and techniques, and continual improvement. It emphasizes a process-based approach and includes workshops to develop process-based checklists. The document outlines auditor competencies including business and technical knowledge, as well as attributes like impartiality and ethical behavior.
This document provides an overview of an upcoming ISO 9001 training course. It introduces the instructor and outlines the course agenda, objectives, and who should attend. The course will cover the history and content of ISO 9001 as well as the new version ISO 9001:2015. It will explain key changes in ISO 9001:2015 around areas like documentation, management responsibilities, and risk-based thinking. The goal is to help businesses understand and effectively implement the new standard to improve efficiency and customer satisfaction.
The document discusses calibration issues affecting an egg production company. It summarizes that production costs have risen and egg yields have fallen, but medium and small egg production has increased to offset some losses. The real problem was identified as inaccurate calibration of the balance scales over time, leading to eggs being misclassified. The company plans to implement a systematic calibration management program to properly monitor, verify, and calibrate instruments on a regular schedule.
An overview of ASQ Quality Auditor (CQA) certification program with tips for passing exam
http://seetharamkandarpa.webnode.in/news/web-series-session-1-overview-of-asq-certified-quality-auditor-conducted-on-21-may-2017/
This presentation gives a bried overview of the various parts & purpose of the ISO 9001:2015 QMS.
It revolves around the PDCA Cycle and useful in Manufacture & construction Industry.
The most valuable Helpful PDF file that extremely can boost your ability to understand well the New version of QMS in accordance to ISO 9001:2015 as well as ease the documentation transition process toward ISO 9001:2015
The document provides an overview of the ISO 9001 quality management standard and certification process. It discusses the key principles and requirements of ISO 9001, including customer focus, leadership, engagement of people, process approach, and continual improvement. It also outlines the certification requirements and critical success factors for organizations going through the ISO 9001 implementation and certification process.
The document outlines a 10 step approach used by Lakshy Management Consultant Pvt. Ltd. to implement ISO 9001 certification. The 10 steps include awareness training, developing a quality policy and objectives, gap analysis, documentation and process design, implementation, internal audits, management reviews, shadow audits, corrective actions, and the final certification audit. Lakshy provides consulting services to guide clients through each step of the ISO 9001 implementation and certification process.
This document provides information about an ISO 9001:2008 Lead Auditor training course, including details about the course content, assessment, delivery style, and auditor requirements. The course covers quality management principles, ISO standards, auditing planning and techniques, and continual improvement. It emphasizes a process-based approach and includes workshops to develop process-based checklists. The document outlines auditor competencies including business and technical knowledge, as well as attributes like impartiality and ethical behavior.
This document provides an overview of an upcoming ISO 9001 training course. It introduces the instructor and outlines the course agenda, objectives, and who should attend. The course will cover the history and content of ISO 9001 as well as the new version ISO 9001:2015. It will explain key changes in ISO 9001:2015 around areas like documentation, management responsibilities, and risk-based thinking. The goal is to help businesses understand and effectively implement the new standard to improve efficiency and customer satisfaction.
The document discusses calibration issues affecting an egg production company. It summarizes that production costs have risen and egg yields have fallen, but medium and small egg production has increased to offset some losses. The real problem was identified as inaccurate calibration of the balance scales over time, leading to eggs being misclassified. The company plans to implement a systematic calibration management program to properly monitor, verify, and calibrate instruments on a regular schedule.
A brief Introduction to ISO 9001 2015-Quality Management SystemSARWAR SALAM
Introduction to Quality Management System ISO 9001-2015 as outlined in EDC Romfor's IMS. Preparation, role and resposibility allocation for Audit purposes.
The document discusses quality management systems and ISO standards. It provides an overview of ISO, including its origins, benefits, and requirements. The main requirements for a quality management system are scope, documentation, management responsibility, resource management, product realization, and measurement and improvement. The document also outlines procedures for documentation, implementation, internal auditing, and registration in accordance with ISO standards.
ISO 9001:2015 Quality Management PrinciplesKaren Sharick
ISO 9001 is an international standard for quality management systems that helps organizations ensure they meet customer and regulatory requirements. A new version, ISO 9001:2015, was recently published with a focus on risk-based thinking and leadership engagement. Implementing an ISO 9001-compliant quality management system can benefit organizations in many ways such as improved customer satisfaction, operational efficiencies, and access to new markets. Certification is not required but can provide third-party validation that an organization meets the standard's requirements.
All the information have the reference of
DAP, Overview of the ISO 9001:2015 QMS, Module 1: Introduction, iso-9001-2015-mod1_intro_to_qms.pdf, date retrieved: September 21, 2019
The document outlines the key clauses of the ISO 9001:2015 quality management standard. It discusses the standard's scope and references in clauses 1-3. Clause 4 covers understanding the organization's context and interested parties. Clause 5 addresses leadership and management commitment. Clause 6 discusses quality planning. Clause 7 covers resource management and documentation. Clause 8 focuses on operational planning, design, and control of outputs. Clause 9 is about performance evaluation through monitoring, measurement, and management review. Finally, clause 10 covers improvement through nonconformity handling and continual improvement.
This document discusses quality assurance in healthcare. It defines quality assurance and related terms like quality control, continuous quality improvement, and total quality management. It describes the key components of quality in healthcare as safety, effectiveness, patient-centeredness, and timeliness. The purposes of quality assurance are to meet customer needs, standardize care, minimize errors, and attain excellence. Nurses play an important role in quality assurance through activities like developing quality monitoring mechanisms, contributing innovations, and participating in improvement efforts.
This document discusses improving supplier quality and addressing the costs of poor quality. It defines cost of poor quality as costs associated with defects, and categorizes these costs. It notes that customer requirements are increasingly stringent, measured in parts per million rather than incidents per thousand. This puts pressure on manufacturers to maintain low defect levels. When defects occur, it increases inspection and production costs for manufacturers. The document also discusses root cause analysis of defects, manufacturer-supplier relationships, and how an external consultancy can help by conducting thorough root cause analysis and working with suppliers to address quality issues.
This document provides an overview of a presentation on quality management systems and ISO standards. It discusses the history and formation of ISO, key ISO standards like ISO 9000 and 9001, benefits of ISO certification like reduced errors and increased customer satisfaction, and sector-specific standards for industries like automotive and telecommunications. The presentation covers topics like quality management principles, documentation requirements, internal audits, and implementing an ISO-compliant quality management system.
This document provides an overview of ISO 9001:2015. It discusses what ISO means, the benefits of ISO standards, quality management principles, the PDCA cycle, and the structure and requirements of ISO 9001:2015. The key points are that ISO establishes internationally recognized standards, ISO 9001 specifies requirements for quality management systems, and the standard comprises 11 clauses that cover the PDCA cycle of plan, do, check, act for continuous improvement.
Chuck Blair, Regional Automotive Program Manager, and Mike Brannock, Automotive SBU Director, go through the highlights of the changes from TS 16949 to IATF 16949.
1) The document discusses leadership requirements in ISO 9001:2015, including demonstrating leadership commitment, establishing a quality policy, and defining organizational roles and responsibilities.
2) Top management must ensure the quality management system is effective and integrated, that resources are available, and that quality objectives align with strategic goals. Customer focus and satisfaction must also be promoted.
3) The quality policy provides a framework for quality objectives and commits the organization to satisfying requirements and continual improvement. It must be communicated and available as documented information.
The document discusses implementing a quality management system according to ISO 9001 standards. It defines key terms like quality management system, process approach, and continuous improvement. It explains that a quality management system manages all organization activities related to quality, focuses on customer satisfaction, and requires documentation, implementation, and review. The quality standard ISO 9001 is process-based and requires planning processes, managing resources, realizing products, and measuring/improving the system.
Quality objectives are specific, measurable targets set by an organization to demonstrate the effectiveness of its quality management system and progress towards its quality policy. Examples of quality objectives include reducing defect and scrap rates, customer complaints, and non-conformances found in internal audits. Objectives should be established for all levels and functions, measured regularly, and not created solely for certification without aiming to improve the quality system.
Use this ppt presentation to educate groups on what is ISO 9001:2015 standard, what are the requirements of ISO 9001:2015 certification, etc.
For more information visit: https://www.globalmanagergroup.com/
The new ISO 9001:2015 committee draft is published and distributed. There are changes which affect organizations who applied this standard. As it is among most famous ISO standards, follow up the changes would be critical and it is time to consider changes which might affect organizations' management systems.
The document discusses ISO 9001, an international standard for quality management systems. It provides an overview of ISO 9001, including its history and timeline, key requirements, benefits, and the revised 2015 version. The standard is applicable to organizations of all sizes and sectors. Certification involves a two-stage audit process to verify the organization's quality management system meets ISO 9001 requirements. Maintaining certification requires ongoing activities like internal audits, corrective actions, and training.
The document discusses the quality management principles as per ISO 9001:2015. It provides explanations of seven principles: 1) Customer Focus, 2) Leadership, 3) Engagement of People, 4) Process Approach, 5) Improvement, 6) Evidence-Based Decision Making, and 7) Relationship Management. It notes some revisions from the previous ISO 9001 standards, including a merging of two principles and renaming of others. The document concludes that awareness of these principles helps understand ISO 9001:2015.
The document provides an overview of the ITIL 4 Foundation course mind map. It summarizes the key topics covered in the ITIL 4 Foundation certification including general management practices, service management practices, creating service value, the service relationship model, external factors, the service value system, the service value chain, service value streams, and the ITIL overview. It also includes an example case study of how ITIL principles could be applied at a car rental company.
Global Manager Group has published this presentation to give information about how AS9100 awareness and auditor training presentation kit helps you.
For more information about AS9100 training kit visit: https://www.globalmanagergroup.com/
Laboratory Information Management Systems (LIMS) software provides an effective solution for managing laboratory operations by linking information systems in a network. Traditional lab methods can lack effectiveness and increase errors and work stoppages. LIMS standardizes operations, validates software, determines quality control, and generates reports to coordinate functions and maintain harmony among employees. While LIMS enhances a lab's potential, it requires training to operate properly and specialized providers like Agaram Technologies can help laboratories implement and manage an effective LIMS solution.
The Association of Public Health Laboratories (APHL) aims to promote public health laboratories through quality laboratory practices. APHL conducted surveys of public health laboratories' Laboratory Information Management Systems (LIMS) which found that most states have multiple LIMS, are seeking to replace aging systems, and exchange data through various methods with limited compatibility. APHL is working with partners to develop interoperable electronic laboratory data exchange networks.
A brief Introduction to ISO 9001 2015-Quality Management SystemSARWAR SALAM
Introduction to Quality Management System ISO 9001-2015 as outlined in EDC Romfor's IMS. Preparation, role and resposibility allocation for Audit purposes.
The document discusses quality management systems and ISO standards. It provides an overview of ISO, including its origins, benefits, and requirements. The main requirements for a quality management system are scope, documentation, management responsibility, resource management, product realization, and measurement and improvement. The document also outlines procedures for documentation, implementation, internal auditing, and registration in accordance with ISO standards.
ISO 9001:2015 Quality Management PrinciplesKaren Sharick
ISO 9001 is an international standard for quality management systems that helps organizations ensure they meet customer and regulatory requirements. A new version, ISO 9001:2015, was recently published with a focus on risk-based thinking and leadership engagement. Implementing an ISO 9001-compliant quality management system can benefit organizations in many ways such as improved customer satisfaction, operational efficiencies, and access to new markets. Certification is not required but can provide third-party validation that an organization meets the standard's requirements.
All the information have the reference of
DAP, Overview of the ISO 9001:2015 QMS, Module 1: Introduction, iso-9001-2015-mod1_intro_to_qms.pdf, date retrieved: September 21, 2019
The document outlines the key clauses of the ISO 9001:2015 quality management standard. It discusses the standard's scope and references in clauses 1-3. Clause 4 covers understanding the organization's context and interested parties. Clause 5 addresses leadership and management commitment. Clause 6 discusses quality planning. Clause 7 covers resource management and documentation. Clause 8 focuses on operational planning, design, and control of outputs. Clause 9 is about performance evaluation through monitoring, measurement, and management review. Finally, clause 10 covers improvement through nonconformity handling and continual improvement.
This document discusses quality assurance in healthcare. It defines quality assurance and related terms like quality control, continuous quality improvement, and total quality management. It describes the key components of quality in healthcare as safety, effectiveness, patient-centeredness, and timeliness. The purposes of quality assurance are to meet customer needs, standardize care, minimize errors, and attain excellence. Nurses play an important role in quality assurance through activities like developing quality monitoring mechanisms, contributing innovations, and participating in improvement efforts.
This document discusses improving supplier quality and addressing the costs of poor quality. It defines cost of poor quality as costs associated with defects, and categorizes these costs. It notes that customer requirements are increasingly stringent, measured in parts per million rather than incidents per thousand. This puts pressure on manufacturers to maintain low defect levels. When defects occur, it increases inspection and production costs for manufacturers. The document also discusses root cause analysis of defects, manufacturer-supplier relationships, and how an external consultancy can help by conducting thorough root cause analysis and working with suppliers to address quality issues.
This document provides an overview of a presentation on quality management systems and ISO standards. It discusses the history and formation of ISO, key ISO standards like ISO 9000 and 9001, benefits of ISO certification like reduced errors and increased customer satisfaction, and sector-specific standards for industries like automotive and telecommunications. The presentation covers topics like quality management principles, documentation requirements, internal audits, and implementing an ISO-compliant quality management system.
This document provides an overview of ISO 9001:2015. It discusses what ISO means, the benefits of ISO standards, quality management principles, the PDCA cycle, and the structure and requirements of ISO 9001:2015. The key points are that ISO establishes internationally recognized standards, ISO 9001 specifies requirements for quality management systems, and the standard comprises 11 clauses that cover the PDCA cycle of plan, do, check, act for continuous improvement.
Chuck Blair, Regional Automotive Program Manager, and Mike Brannock, Automotive SBU Director, go through the highlights of the changes from TS 16949 to IATF 16949.
1) The document discusses leadership requirements in ISO 9001:2015, including demonstrating leadership commitment, establishing a quality policy, and defining organizational roles and responsibilities.
2) Top management must ensure the quality management system is effective and integrated, that resources are available, and that quality objectives align with strategic goals. Customer focus and satisfaction must also be promoted.
3) The quality policy provides a framework for quality objectives and commits the organization to satisfying requirements and continual improvement. It must be communicated and available as documented information.
The document discusses implementing a quality management system according to ISO 9001 standards. It defines key terms like quality management system, process approach, and continuous improvement. It explains that a quality management system manages all organization activities related to quality, focuses on customer satisfaction, and requires documentation, implementation, and review. The quality standard ISO 9001 is process-based and requires planning processes, managing resources, realizing products, and measuring/improving the system.
Quality objectives are specific, measurable targets set by an organization to demonstrate the effectiveness of its quality management system and progress towards its quality policy. Examples of quality objectives include reducing defect and scrap rates, customer complaints, and non-conformances found in internal audits. Objectives should be established for all levels and functions, measured regularly, and not created solely for certification without aiming to improve the quality system.
Use this ppt presentation to educate groups on what is ISO 9001:2015 standard, what are the requirements of ISO 9001:2015 certification, etc.
For more information visit: https://www.globalmanagergroup.com/
The new ISO 9001:2015 committee draft is published and distributed. There are changes which affect organizations who applied this standard. As it is among most famous ISO standards, follow up the changes would be critical and it is time to consider changes which might affect organizations' management systems.
The document discusses ISO 9001, an international standard for quality management systems. It provides an overview of ISO 9001, including its history and timeline, key requirements, benefits, and the revised 2015 version. The standard is applicable to organizations of all sizes and sectors. Certification involves a two-stage audit process to verify the organization's quality management system meets ISO 9001 requirements. Maintaining certification requires ongoing activities like internal audits, corrective actions, and training.
The document discusses the quality management principles as per ISO 9001:2015. It provides explanations of seven principles: 1) Customer Focus, 2) Leadership, 3) Engagement of People, 4) Process Approach, 5) Improvement, 6) Evidence-Based Decision Making, and 7) Relationship Management. It notes some revisions from the previous ISO 9001 standards, including a merging of two principles and renaming of others. The document concludes that awareness of these principles helps understand ISO 9001:2015.
The document provides an overview of the ITIL 4 Foundation course mind map. It summarizes the key topics covered in the ITIL 4 Foundation certification including general management practices, service management practices, creating service value, the service relationship model, external factors, the service value system, the service value chain, service value streams, and the ITIL overview. It also includes an example case study of how ITIL principles could be applied at a car rental company.
Global Manager Group has published this presentation to give information about how AS9100 awareness and auditor training presentation kit helps you.
For more information about AS9100 training kit visit: https://www.globalmanagergroup.com/
Laboratory Information Management Systems (LIMS) software provides an effective solution for managing laboratory operations by linking information systems in a network. Traditional lab methods can lack effectiveness and increase errors and work stoppages. LIMS standardizes operations, validates software, determines quality control, and generates reports to coordinate functions and maintain harmony among employees. While LIMS enhances a lab's potential, it requires training to operate properly and specialized providers like Agaram Technologies can help laboratories implement and manage an effective LIMS solution.
The Association of Public Health Laboratories (APHL) aims to promote public health laboratories through quality laboratory practices. APHL conducted surveys of public health laboratories' Laboratory Information Management Systems (LIMS) which found that most states have multiple LIMS, are seeking to replace aging systems, and exchange data through various methods with limited compatibility. APHL is working with partners to develop interoperable electronic laboratory data exchange networks.
The document discusses the history and operations of laboratory information management systems (LIMS). It explains that LIMS emerged in the 1970s to streamline sample management and reporting in laboratories. The first commercial LIMS used centralized minicomputers, while newer versions tap into relational databases and incorporate features like electronic data exchange. A LIMS manages essential laboratory functions like sample receipt and tracking, scheduling analyses, processing data, and reporting results. It also facilitates the storage and transfer of electronic data and adheres to various industry standards.
Laboratory Information Management System (LIMS)mariam1020
Business logistics costs in the United States rose from $1.183 trillion in 2005 to $1.305 trillion in 2006 and $1.4 trillion in 2007. A Laboratory Information Management System (LIMS) is a software system that stores and manages laboratory data and sample information to improve efficiency. Implementing a LIMS can provide benefits such as reduced costs, improved data quality, and increased productivity.
This document discusses Laboratory Information Management Systems (LIMS). It begins by defining LIMS as a method laboratories use to manage data and disseminate results. It then discusses why LIMS are important for managing the information explosion, ensuring quality assurance, and reducing errors. The document outlines different types of laboratories that use LIMS, including research, testing, and manufacturing labs. It concludes by discussing how laboratories can determine their LIMS needs and options for acquiring a system through a systems analysis approach.
By leveraging Complaints Management Software and viewing complaints as a learning opportunity, businesses can turn a challenge into a competitive advantage. You can invest in complaints software that can seamlessly integrate with your existing quality management software to build a closed-loop system.
Prism eSolutions presents its Prism quality management software. The software provides an integrated platform for automating ISO compliance through modules for document control, project management, audits, and more. It allows companies to efficiently address quality management needs. Prism's software saves time and money compared to traditional methods. It is a customizable solution available both hosted through Prism or installed on clients' servers.
The document discusses requirements management practices for new product introductions. It emphasizes the importance of clearly documenting customer needs and linking them to product features, capabilities, and tests throughout the design and development process. A stage-gate process is used to drive cross-functional collaboration and ensure customer expectations are met. Key questions are provided for leadership reviews at each stage to assess alignment with customer needs and authorize moving to the next stage of product development.
This document provides information about E&E Systems Co, an Iranian company that provides compliance management software solutions for ISO management system standards. It details the company's history, vision, values, products and services. The key products are Document Management Software, Corrective and Preventive Action Management Software, Supplier Evaluation Management Software, and After-Sales Service Management Software. The document also lists some featured customers across various industries that use E&E's software solutions.
Maveric Systems offers several platforms to help banks with digital banking applications and software testing:
- AccelGate is a platform-led testing solution that enables banks to thoroughly test their digital applications to deliver defect-free, cost-efficient applications faster. It tests applications for functionality, compatibility, performance, and usability.
- Requirements Maturity Assessment Model examines an organization's requirements development and management processes and provides recommendations to improve based on industry best practices. It aims to reduce project failures and defects.
- Test Basis is a proprietary requirements definition workbench that enhances automation testing by consolidating scattered requirements specifications. It identifies missing requirements and facilitates validation of tester understanding. It translates requirements into test designs.
The aim is to be a one stop service provider for consulting and support services related to compliance, validation, Computerized System Validation, IT Infrastructure Qualification and IT Solutions catering to clients in the life sciences industry. The main objective is to provide services that enhance current operations and bring the knowledge and experience needed to maintain, manage and control related services.
The philosophy of IVY Works is to be transparent, open and work with our Clients as part of their teams to achieve set objectives and goals.
Experience: Extensive experience among the founders in regulatory compliance, validation, CSV and IT Solutions. All consultants have relevant experiences in the life sciences industries with exposure to the whole gamut of operations (manufacturing, labs, IT, regulatory).
Exposure: Founders and Consultants have worked with a majority of the top ten Pharmaceutical companies in lead roles to manage and also better develop, implement and validate compliance processes. Have worked with clients in North America, Europe & Asia.
Performance: Proven track record of delivering ahead of budget and timelines for a variety of projects/ programs
Delivery: Ability to take on projects of any size – with the same emphasis on project delivery and management
Lisa Burdick has over 15 years of experience in quality and regulatory roles within ISO 13485 and FDA regulated environments. She has extensive experience with quality documentation, lot release, sterilization processes, auditing, and calibration systems. Currently she works as a Senior Quality Systems Specialist at Valeritas, where she manages lot release, sterilization processes, documentation systems, auditing, and corrective and preventative action programs.
The document provides an overview of DataR, a quality control program created using Six Sigma principles. DataR aims to increase profitability for companies by having a dedicated quality control program overseen by senior management. It operates with zero margin of error and measures results to ensure quality. DataR implements a standardized process across facilities to eliminate variables and ensure consistent quality checks and data verification for repaired devices.
Vidhur Racharla has over 4 years of experience implementing and supporting LabWare LIMS systems. He has successfully implemented LIMS systems for pharmaceutical companies in Saudi Arabia and the United States. His experience includes configuring modules, developing reports, integrating other systems, and providing training and support to users. He aims to continue working in challenging roles that allow him to grow professionally.
This document provides information about an upcoming conference on electronic GMP systems. The conference will take place from March 18-20, 2015 in Prague, Czech Republic and will focus on the specification, implementation, and validation of electronic GMP systems. It will provide learning objectives on identifying the best systems, managing costs and risks, efficient implementation, and achieving promised benefits in a compliant manner. Experts will present on topics like new regulatory guidance, user requirements, project management, and ensuring data integrity. Attendees will participate in workshops to practice applying the concepts to real-world examples.
How Business Process Assurance Can Enhance Quality When Applying Agile Method...Cognizant
As organizations increasingly go digital, implementing business process assurance (BPA) in an Agile development environment helps ensure that continuity is maintained, and that quality and speed are balanced.
GenesisLab360, a laboratory information management system (LIMS), the strongest and more flexible LIMS/LIS Platform that is tailored not only to manage an organization´s laboratory information but to provide an integrated informatics solution and platform that allow for outstanding laboratory capabilities for workflow management, optimizing productivity and operating cost with increasing quality.
From Data to Insights: How IT Operations Data Can Boost QualityCognizant
By leveraging highly-analyzed operational data - the voice of customers, machines and tests - quality assurance (QA) and IT groups can derive major gains in quality of apps and in user experience.
Divya B Ravichandran is a senior software engineer with over 5 years of experience in testing robust applications across various industries. She has expertise in agile and waterfall testing methodologies and has experience preparing test plans, cases, reports, and delivering projects on time. Her skills include functional, database, system, regression and end-to-end testing. She has worked on projects in the insurance and survey domains using tools like Jira, ALM, and Visual Studio. She is proficient in testing methodologies, SQL, and web services testing. She aims to continuously enhance her and her team's knowledge.
This document discusses how ALM (Application Lifecycle Management) tools can help project managers through Kanban boards, dashboards and reports, and traceability features. It focuses on Intland Software's codeBeamer ALM platform, which provides holistic and compliant processes for industries like medical, automotive and aviation. The presentation covers how codeBeamer supports advanced workflows and visualization, electronic Kanban boards, configurable dashboards and reporting, and traceability across the lifecycle. It also briefly highlights codeBeamer clients and a live demo of the tool.
This document provides information about free quality management system software, including descriptions of various quality management tools and topics. It discusses popular free quality management system software and outlines the contents and benefits of MasterControl's quality management software system. The system consists of integrated applications that automate and streamline document control, corrective and preventive action, change control, training management, nonconformance handling, quality auditing, customer complaints, and other quality processes. Common quality management tools like check sheets, control charts, Pareto charts, scatter plots, Ishikawa diagrams, and histograms are also explained. Other related quality management topics that could be covered in PDF downloads are listed.
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(3) AI Partner & Profit Review: https://sumonreview.com/ai-partner-profit-review
(4) AI Ebook Suite Review: https://sumonreview.com/ai-ebook-suite-review
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SQL has attained widespread adoption, but Business Intelligence tools still use their own higher level languages based upon a multidimensional paradigm. Composable calculations are what is missing from SQL, and we propose a new kind of column, called a measure, that attaches a calculation to a table. Like regular tables, tables with measures are composable and closed when used in queries.
SQL-with-measures has the power, conciseness and reusability of multidimensional languages but retains SQL semantics. Measure invocations can be expanded in place to simple, clear SQL.
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A talk at SIGMOD, June 9–15, 2024, Santiago, Chile
Authors: Julian Hyde (Google) and John Fremlin (Google)
https://doi.org/10.1145/3626246.3653374
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We implement context-sensitive pointer/alias and dataflow analyses on Graspan. An evaluation of these analyses on large codebases such as Linux shows that their Graspan implementations scale to millions of lines of code and are much simpler than their original implementations.
These analyses were used to augment the existing checkers; these augmented checkers found 132 new NULL pointer bugs and 1308 unnecessary NULL tests in Linux 4.4.0-rc5, PostgreSQL 8.3.9, and Apache httpd 2.2.18.
- Accepted in ASPLOS ‘17, Xi’an, China.
- Featured in the tutorial, Systemized Program Analyses: A Big Data Perspective on Static Analysis Scalability, ASPLOS ‘17.
- Invited for presentation at SoCal PLS ‘16.
- Invited for poster presentation at PLDI SRC ‘16.
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The purpose of this presentation is to provide an overview of how you can use AI from XSLT, XQuery, Schematron, or XML Refactoring operations, the potential benefits of using AI, and some of the challenges we face.
Artificia Intellicence and XPath Extension Functions
Lab automation with Calibration LIMS
1. Solution Proposal for Calibration Lab
Labsols CAL-LIMS meets the complex requirements of the modern
calibration laboratories that allow your business to be more
competitive, bring accurate lab operations, achieve operational
efficiencies and meet your regulatory commitments more easily.
2. Key Facts:Challenges:Labsols Calibration-LIMS SolutionLabsols Calibration-LIMS Solution
Measurement related operations have been
estimated around 3% and 6% of GDP in
industrial countries.
Neglecting calibration can lead to unscheduled
production downtime,qaulity issues, product
recalls and rework.
Global calibration Services market was valued at
USD 1.1 billion in 2013 and is estimated to reach
a market worth of USD 2.1 billion in 2020
growing at a CAGR of 10.% from 2014 to 2020.
Growth in the market driven by factors such as the
widespread adoption of quality standards, periodic
calibrations under ISO regulations, and
innovations in service delivery mechanisms
Meeting industry standard quality
requirement: Quality, Service and Profit (QSP) seem
to be in opposition. yet in order to be competitive and
successful, your lab must continually produce higher
quality, better service and yes, still be profitable.
Complexity in the standards and calibration
procedures:Laboratories are expected to meet
industry standards and handling various calibration
types and procedures
Traceability: Demand for laboratories to demonstrate
traceability of their tests and measurements to
international standards;
Measurement Uncertainty: Increased
demand(from accreditation bodies and others) that
laboratories will have determined the measurement
uncertainty of the tests and calibrations they perform.
Documentation: Increased sophistication in the
documents affecting the production of reference
materials and certified reference materials.
Sales Order, Workbook, Sample Management,
Calibrate-Result Entry, Shipment, Billing, etc:
Organized equipment sample inventory with simple
and advanced search in just one click.
Keeps track of all calibration tests and analysis conducted on
each sample.
Covers range of calibration procedures and types of
calibrations
Manages Sales orders with shipment and billing, etc
Advance Reporting, KPI, Certificates, Graphs:
Powerful Reporting providing critical facts, Reports can
be classified according to various users and tailored
needs both analytical and graphical.
Quick Documentation & Communication:
Effective document and data management to allow search and
access all the relevant and critical data in quick time
Helps users to create communication templates and pre assign
to users to be sent automatically according to an event
Optimum security for both elements all the time
Customer Platform:
Allowing lab customers to enter test requests and to retrieve
reports, pay invoices and to get support from the lab in no time,
access to information and support.
Calibration LIMS – Solution for Industry Challenges:
For Information, drop an email to: sapon@calibration-lims.co.uk
3. Solutions:Solutions:
Key Expectation from Calibration Lab & Labsols Solution:
Solutions:Solutions:
Solutions:Solutions:
An equipment /sample is not helping if it is out of
business.
Turnaround time for services are getting shorter for
competiveness .
Rush services, including three day and same day
calibrations are available in some situations
Sampling- Quick submission, receipt, work list,
inventory, review approval & allocation.
Calibrate/Testing- Instant test allocation, workflow
and workbook creation with simple, result entry,
certificate generation, customized reports.
Provide quick important calibration
certificates for auditors.
Review opportunity for clients to view
equipments due for calibration and
deactivate equipments you have taken out of service.
Inbuilt templates of certificates and option for
customizing logos and other features as per
clients requirement instantly
Issue & Support Management:
Issue logging and tracking against sample jobs,
others .
.
Intimation to customers as soon as equipment is received.
Availability of certificate via portal.
Details of shipment with notifications.
Our solution can be configured for automatic
notification as soon as sales order entry is made.
Shipment/billing details can be modified instantly if
required.
Expectations Labsols CAL-LIMS
SpeedSpeed
Certificate on DemandCertificate on Demand
Calibration Cycle CoverageCalibration Cycle Coverage
For Information, drop an email to: sapon@calibration-lims.co.uk
4. Some more expectation from customer side:
Mobility
Inbuilt Audit trial to track the entire history of login
processes changes made to every activity
Compatible with any compliance and accredited labs
including A2LA to ISO/IEC 17025:2005 calibration lab who
performing in-labs and on-site calibrations.
With our solution your data is backed up as per your
requirement and secured privacy.
Accreditations & Audit
Labsols Mobile SolutionLabsols Mobile Solution CAL-LIMS SolutionCAL-LIMS Solution
Helps to update customers instantly about any
issues , alerts, dues, etc
Provides interface to check sample status at each
stage and check reports and more
Display social networking Links and much more.
Helps to send automatic reports to customers in
real time.etc
Accreditation proves your lab is traceable.
An audit proof laboratory depicts their work is
right compared to other labs.
Customers are slowly becoming conscious about
there data security and calibration labs offer.
Certification available on smart phone.
Alert and notifications on there equipment testing,
due calibrations, due payment
Calibration trend analysis on mobile and more.
For Information, drop an email to: sapon@calibration-lims.co.uk
5. Key Solutions :
Supports calibration procedures of all major
equipments under a roof of a single application.
Reduces Lag time by automating sampling,
testing ,result entry functions.
Real time feedback on sample deviation and real
time monitoring to control the calibration
process.
Reduces paper handling and manual processes in
a calibration lab which includes paper records
from job observation to certificates.
Internal Solutions and benefits from CAL-LIMS:
Multiple lab operation can be seen from single
view resulting in optimized workload and
equitable distribution to operators and
engineers.
For Information, drop an email to: sapon@calibration-lims.co.uk
6. Excellent Sample Management Advance Reporting Statistical Analytics
Quick Documenting & Communication Organized Customer Platform
Organized sample inventory with simple and
advanced search in just one click .
Keeps track of all tests and analysis
conducted on each sample by tightly
integrating all the steps and all processes
Stage wise sample analysis recording various
stages of the testing process and all
information related to each stages and more
Powerful Reporting providing critical facts for
organization's better analysis and decision
making
Reports can be classified according to various
users and tailored needs – getting clear
information of various details in a glimpse
Provides both analytical and graphical reports
which give a detailed insight of analysis
Advanced analytics dashboard showing all
testing related activities along with results
and analysis
SPC chart is fully functional in providing
minute Statistical Report, Sample analysis
data
Historical analysis and condition
monitoring data in flexible formats
Provide effective document and data management to
allow search and access all the relevant and critical data
in quick time
Equipped with powerful communication tool that will
enable users to create communication templates and pre
assign to users to be sent automatically according to an
event
Optimum security for both elements all the time
Allowing lab customers to enter test requests and to
retrieve reports, pay invoices and to get support from
the lab in no time
Allowing customer the opportunity to access
information pertaining to their samples easily from
anywhere in their smart phone or tablet
Allowing customer to log their issues online and giving
instant support in minutes
For Information, drop an email to: sapon@labsols.com
How CAL-LIMS is going to help:
For Information, drop an email to: sapon@calibration-lims.co.uk
7. CLOUD
COMPUTING
POWERFUL
REPORTING
STATISTICAL PROCESS
CONTROL (SPC)
DOCUMENT & LOG
MANAGEMENT
SAMPLE & TEST
MANAGEMENT
MOBILE INTEGRITY & OPR
INTELLIGENCE
For Information, drop an email to: sapon@labsols.com
Features that makes our LIMS standout:
For Information, drop an email to: sapon@calibration-lims.co.uk
8. Comes with add-on – Customer facing portal for lab customers:
Key CUSTOMER modules – Glimpses
My Dashboard
Customers can view Lab
Performance
My Samples My Reports
My Invoices My Enquiry My Documents
Customers can view their Samples
& Give test request
Customers can view their reports
on various parameters
Customers can view their lab
invoice, outstanding & Pay online
Customers can lodge Enquiry,
Issue & get instant support
Customers can view / download
documents in different formats
For Information, drop an email to: sapon@labsols.com For Information, drop an email to: sapon@calibration-lims.co.uk
9. Add-on – Mobile App for lab operations Glimpses:
ADVANCED Push Notification and various alerts to
Lab user & customer in real time
TRACK samples, result and analysis in Mobile
BRINGS live updates and reports from the
Laboratory
PROVISION to enter results in tablets on the go
POWERED by best reporting tool Quinn Curtis
GENERATE and view multiple Reports & Analytics
ADD Photos, Videos and Geographic Location
during sample collection
COMMUNICATE instantly with Lab and take key
Decisions
STAY connected with the laboratory on the MOVE
PERFORMANCE dashboard with improved KPI for
stakeholders to check lab performance
INTEGRATE instantly with existing system in
minutes
LOCATE Ports on Google maps
OTHER interesting features
VIEW Certificates other Report PDFs in mobile RECEIVE Sample – At docking Stations
For Information, drop an email to: sapon@labsols.com For Information, drop an email to: sapon@calibration-lims.co.uk
10. For Information, drop an email to: sapon@labsols.com
Snapshots Mobile Application:
Visit for more details:
http://calibration-lims.co.uk/Index.aspx