Alternatives to Ansys medini analyze

HSI Donesafe redefines EHS management with a no-code, cloud-based platform that transforms complex processes into streamlined, user-friendly workflows. Trusted across industries, Donesafe consolidates tracking, management, and reporting into one accessible platform, making compliance simpler and safety more effective. Donesafe’s adaptable design allows teams to customize workflows, forms, and dashboards to meet evolving compliance needs. With tools for incident reporting, audits, training, and risk assessment, staying ahead of regulatory changes has never been easier. Key Features: - Customizable workflows to align with regulations - Real-time insights for live safety tracking - Scalable design that grows with your team - Streamlined compliance tools for smooth audits and reporting Empower your EHS team to achieve safety excellence with HSI Donesafe.

Intelex delivers a unified software system for overseeing Environmental, Health, Safety, and Quality (EHSQ) initiatives. Its expandable platform is crafted to consolidate, oversee, and scrutinize EHS and Quality data comprehensively. The solution works on any device to meet the realities of your workplace. With Intelex, your organization can: Elevate your EHSQ program outcomes by supervising workflows for superior performance and command. Discern patterns and propensities through goal-setting to deepen understanding and improve decision-making in your EHSQ program. Diminish occurrences and cut down on administrative tasks by efficiently supervising, managing, refining, and extracting insights from your safety data via our intuitive safety software. Simplify the management and reporting of air, water, and waste emissions, and oversee environmental outputs to fulfill sustainability objectives. Foster ongoing improvements in quality by seamlessly logging and monitoring all instances of nonconformity within a unified, web-based system. Investigate trends across various departments, sites, or locations. Intelex can help you manage compliance with international standards and regulations such as: OSHA, WCB, ISO 45001, EPA, ISO

It is difficult to make data available and actionable when a manufacturing site has many processes. As operations grow, it is becoming more difficult to comply with safety, quality, and environmental regulations. Manufacturing is built on predictability and reliability. Manufacturing by nature is all in the execution of established processes. TenForce was built from the feedback of our clients to map the operational reality in a plant.

𝗕𝗤𝗥'𝘀 𝘀𝗼𝗳𝘁𝘄𝗮𝗿𝗲 𝘀𝘂𝗶𝘁𝗲 𝗽𝗿𝗼𝘃𝗶𝗱𝗲𝘀 𝗽𝗮𝘁𝗲𝗻𝘁𝗲𝗱 𝗮𝘂𝘁𝗼𝗺𝗮𝘁𝗲𝗱 𝗲𝗹𝗲𝗰𝘁𝗿𝗼𝗻𝗶𝗰 𝗱𝗲𝘀𝗶𝗴𝗻 𝗮𝗻𝗮𝗹𝘆𝘀𝗶𝘀 𝗮𝗻𝗱 𝗼𝗽𝘁𝗶𝗺𝗶𝘇𝗮𝘁𝗶𝗼𝗻 𝘁𝗼𝗼𝗹𝘀 𝘁𝗼 𝘀𝘁𝗿𝗲𝗮𝗺𝗹𝗶𝗻𝗲 𝘆𝗼𝘂𝗿 𝗱𝗲𝘀𝗶𝗴𝗻𝘀: 𝗦𝘆𝗻𝘁𝗵𝗲𝗹𝘆𝘇𝗲𝗿𝗧𝗠 𝗘𝗖𝗔𝗗 𝗣𝗹𝘂𝗴𝗶𝗻 turbocharges PCB design with real-time stress analysis, derating, and thermal simulation. Its seamless integration into ECAD systems ensures optimal component selection and prevents costly errors. 𝗳𝗶𝗫𝘁𝗿𝗲𝘀𝘀® is your reliability engineering powerhouse. With advanced FMECA, stress, and failure predictions, you can extend product lifespan and minimize downtime. Combined with Synthelyzer™, it delivers unparalleled design optimization. 𝗖𝗶𝗿𝗰𝘂𝗶𝘁𝗛𝗮𝘄𝗸™accelerates time-to-market by detecting design flaws early in the process. Its advanced verification capabilities and stress analysis provide a robust foundation for reliable products. 𝗮𝗽𝗺𝗢𝗽𝘁𝗶𝗺𝗶𝘇𝗲𝗿® maximizes asset value and operational efficiency. Through LCC analysis and predictive maintenance, you'll reduce costs, optimize spare parts inventory, and ensure uninterrupted operations. 𝗖𝗔𝗥𝗘® ensures product safety and regulatory compliance. Our comprehensive

ReliaSoft provides a powerful set of reliability software solutions that facilitate a comprehensive range of reliability engineering modeling techniques and analysis techniques. We are the leading provider of reliability solutions for product testing, design, maintenance strategies and optimization. Our products support a variety of reliability and maintainability techniques, including life data analysis, accelerated lifetime testing, system modeling and RAM analysis. We also support reliability growth, FRACAS analysis, FMEA analysis and RCM analysis. These tools help you improve the reliability of your products and processes, and optimize maintenance planning.

TLM QMS Software is a powerful and robust quality, risk and material management software (QMS) which is validated and 21 CFR Part 11 compliant. TLM is a cutting-edge, all-in-one quality management system that can be customized to integrate with online CRM software, QuickBooks or ERP databases. Total Lean Management (TLM) QMS Software is specifically intended to be a low cost, highly integrated, flexible and continuously improving landscape to which specialty systems can be added where needed to create the digital business landscape that enables work flows the way your company needs them to work.

Visure Solutions, Inc., a leading provider in requirements management tool suites, offers a comprehensive collaborative ALM Platform to system engineering industries. Visure's value proposition includes the complete innovative technology in key functions: standard compliance with safety-critical and business critical systems. - Traceability and Requirements Management - Test Management - Issue and Bug Tracking - Risk Management - Collaboration Management - Centralized data base, Review/Approval process - Certification Management (Support for many Standard Templates ISO26262, IEC62304 and IEC61508, CENELEC50128), DO178/C FMEA, SPICE, CMMI, CENELEC50128, CENELEC50128, DO178/C. + Tool Qualification Package - Configuration Management, Baselining and History Tracking, Requirements versioning - Dashboards + Report Customization - Integrated with DOORS and Jama, Siemens Polarion. PTC, Perforce. JIRA. Enterprise Architect. HP ALM. Microfocus ALM. PTC. TFS. Word, Excel. Test RT, RTRT. VectorCAST. LDRA.

Unify quality processes with QT9's all-in-one cloud-based QMS Software Suite. QT9 QMS is a user-friendly quality management software that includes 25+ modules with unlimited scalability. Automate ISO & FDA Compliance with email alerts, To Do lists and FDA 21 CFR Part 11 Compliant Electronic Approvals. QT9 QMS enables Life Sciences, Biotechnology Companies, Medical Device Manufacturers and Pharmaceutical Companies to digitally transform operations. Get real-time status updates and visualize quality metrics up-to-the-minute. QT9 QMS comes with built-in document control, revision-level controls, corrective actions (CAPAs), Nonconforming products and more. Advance product releases with Deviation Management, Engineering Change Orders, FMEA, Inspection Management Modules Included. Go paperless & put time-consuming tasks on autopilot. QT9 QMS comes ready-to-use. Get a free product tour! Start a Free Trial. Visit QT9qms.com

The SBS Quality Database is a simple, inexpensive, ISO 9001 compliant software program that allows small businesses to efficiency manage the Quality Management System or QMS. The database tracks corrective actions, preventive actions (CAPA), internal audits, safety improvement, supplier corrective actions, continual improvement projects. Compile and analyze Customer Survey results. Identify and minimized risk using the risk management module (FMEA & SWOT analysis) . Document QMS review meetings and results. Document interested parties as part of the Context of the organization. Use the dashboard for a quick view of the overall performance. Cloud based or locally installed options are available. The program is ideal for small businesses striving for ISO 9001:2015, API Q1, AS9100, or TS16949 compliance. Free demo downloads are available from our website so you may try before your buy.

Asset-intensive, high-hazard facilities are susceptible to risks. This is especially true if the risk data set contains a lot of process safety risk. It is difficult to assess and standardize all sources of risk in support of resource-intensive facilities. Sphera's PHA Pro provides a framework, configurable methods and risk assessment workflows that can be used to help organizations standardize and document risk assessment data and ensure proper controls. Our PHA-Pro software, which is the most widely used and respected hazard identification tool and risk assessment tool, can be used to strengthen the risk assessment process. It helps to identify, assess, and control the effect of process-related risks. Our facilitators are experts in risk assessment and have extensive experience using any methodology. HAZOP, What/If FMEA, FMECA Revalidation of the PHA Workplace Job Safety Analysis (JSA). Layers of Protection Analysis and Safety Integrity Levels (SIL). SVA

Failure Mode and Effects Analysis (FMEA) is a systematic technique aimed at identifying potential failures in a given system, along with their causes and consequences. This approach proves to be a powerful tool in enhancing quality management processes. It is essential to adhere to standards set by organizations such as ISO, AIAG, and VDA. Ensuring data consistency is crucial, particularly in the control plan and process flow diagram. Additionally, one must possess the capability to conduct various analyses, including PFMEA and DFMEA, while also being familiar with RPFMEA, LFMEA, MFMEA, SwFMEA, and UFMEA methodologies. This breadth of analysis can significantly improve risk assessment and decision-making in product development and manufacturing.

Knowllence acts as a risk management integrator, providing software, training, and consulting services that ensure effective quality, safety, and environmental (QSE) risk management. Safeguard your employees by managing safety through comprehensive documentation, arduousness assessments, and chemical risk evaluations. Enhance your design process with robust methodologies like functional analyses, Failure Modes and Effects Analysis (FMEA), and Fault Tree Analysis (FTA). Ensure the reliability of your industrialization phase by utilizing tools such as AMDEC Process FMEA and establishing a meticulous monitoring plan. Align your risk control measures with ISO 14971 standards for the design and safety of your medical devices. Our team is adept at understanding your specific methodologies and can tailor the configuration of our software to align seamlessly with your existing standards and processes. We offer a comprehensive service designed to streamline your work sessions and risk assessments, empowering you to advance your projects while maintaining a sustainable system: you retain control over the study and the action plans within an efficient, user-friendly software environment. By partnering with us, you can enhance your organization's ability to manage risks effectively and ensure compliance with industry requirements.

SoftExpert FMEA is a comprehensive software solution designed for organizations to effectively oversee Failure Modes and Effects Analysis. By adopting a proactive stance, it allows businesses to forecast potential defects, thereby ensuring the quality of their outputs. This methodology can be utilized across various domains, including products, processes, departments, and assets, leading to a reduction in engineering workloads while simultaneously enhancing machine performance and resource availability through the evaluation and improvement of high-risk elements. The software consistently tracks failures identified during the FMEA process, providing users with detailed reports and visual representations that feature key metrics such as severity and risk priority, which pinpoint critical causes at any given time. Ultimately, this solution plays a vital role in bolstering product safety and dependability, which, in turn, fosters greater customer satisfaction and loyalty. Moreover, by streamlining the analysis process, it empowers teams to make informed decisions that contribute to continuous improvement.

Monitoring quality risk effectively is challenging without a comprehensive knowledge management system. To tackle this, it is essential to establish processes that can proficiently identify, capture, manage, and disseminate vital documents and information. Sphera’s FMEA-Pro software provides a flexible framework that accommodates various FMEA methodologies, along with specialized features for managing risk data, ensuring that appropriate controls are implemented. This software connects essential quality information throughout design and manufacturing processes, facilitating the attainment of the expected quality standards set by your customers. Furthermore, Sphera’s FMEA-Pro software contributes to improving profitability by employing a uniform, standardized approach to thoroughly evaluate inherent risks. Additionally, Sphera's enterprise Advanced Risk Assessment empowers organizations to consistently pinpoint, evaluate, and mitigate the effects of operational risks effectively. By doing so, it enhances overall operational efficiency and resilience in the face of potential challenges.

PLATO e1ns serves as the primary platform for effectively designing the product development process. By ensuring transparency in development processes, fostering a shared understanding of the system, and promoting efficient, interconnected collaboration, it lays the groundwork for economical, swift, and successful product development. This system is tailored for the optimal structuring of the product development process (PDP). With e1ns, PLATO has introduced a solution that is especially beneficial during the initial phases of PDP, where the groundwork for minimizing costs and risks is established. e1ns integrates various methods and development stages into a cohesive system. Through the lens of system model modeling (SysML), each discipline—including mechanical, software, and electrical—benefits from a "Single Point of Information," allowing for centralized and immediate access to all interconnected data and actions within the product development process via a web browser. Furthermore, we will create a bespoke methods framework tailored specifically to address the unique requirements of your development process, ensuring optimal outcomes. This personalized approach enhances the overall effectiveness and adaptability of your product development efforts.

We provide quality management software, offering comprehensive QM solutions tailored for all quality-related tasks, a tradition we've upheld for 25 years. As experts in the field, we have created a versatile quality management solution through our modular software, BabtecQ. Additionally, we present Babtec Qube, a cloud-based platform designed to facilitate collaboration with your suppliers and customers for effective management of your quality tasks. Our offerings empower you to visualize the complete spectrum of quality processes, both within your organization and with external partners, for a quality experience you will be eager to share. If you're interested in enhancing your understanding of quality management principles, you've found the perfect resource! Our knowledge pages offer insights into various topics, such as complaint management and the 8D report. Furthermore, the System FMEA, often referred to as system analysis, serves as a critical component of the FMEA (Failure Mode and Effects Analysis) process, focusing on the evaluation of an entire system to ensure that all individual components function together seamlessly. As you explore these resources, you will gain valuable insights into the intricacies of quality management, equipping you with the knowledge to implement effective practices in your organization.

Integrated EV/AV platform for meeting Functional Safety (ISO 26262) and Automotive SPICE® standards. Develop structure and architecture diagrams, interface functions matrices, p­diagram, and other related tasks. SysML/UML Diagrams, HARA, Hazard And Risk Analysis, technical safety concepts, hardware-software design (HIS) and more can be managed and developed. Supports team collaboration and the development of EV/AV work products. An integrated platform that allows you to manage functional safety plans and cybersecurity (CySe), plans, Automotive SPICE®, software project plans plans, APQP/PPAP/NPD planning, and many other things. Track NPD/APQP projects – track resources, timelines and deliverables. Real-time monitoring of program status and collaboration. Project management, APQP critical pathways, project reviews, and other tasks are all handled easily.

Create a simple, efficient Quality Management System (QMS). You can install on your local server, or use our Cloud QMS solution. ISO 9001:2015 requires risk-based thinking. Risk Assessment: Failure Modes Analysis (FMEA) Implement risk-based strategies for ISO 9001, ISO 14971. Identify failure modes for each item or process. Identify the effects and severity. Identify the causes and frequency. Identify current controls and detection levels. Multiple actions should be taken in response to this failure mode. Assign owners and due dates. Establish verification and validation criteria. Management approval can be obtained by electronic signature. User login: Define passwords and privileges. Rich set of reports. Track open actions and delinquent due date. Microsoft Access is free to download. To further analyze the data, export it to Excel. Common, easy-to-use software platform

The most comprehensive suite of Health & Safety software solutions will streamline your processes and help you manage the risks. ProcessMAP helps companies achieve consistency and provides real-time insights to improve their Health & Safety performance. Standardize, streamline, and track the processes required to comply with various regulations and compliance frameworks. Built-in alerts, robust CAPA Management, and advanced reporting capabilities increase accountability and provide visibility across an organization. They also make it easier to be ready for inspections and audits. The correlation of safety and claims data can reduce risk. Analyze the root causes of claims and events to identify and mitigate risk. Our platform reduces risk by stopping claims from happening. The industry's best cloud platform for sustainability management and metrics reporting. Streamline the collection, verification and analysis of company-wide KPIs.

ISOQualitas.PLM, an all-in-one QMS program, helps automotive suppliers efficiently capture product development, design, and manufacturing information. It can create, print, or store quality information and documents including Control Plans, CSRs and Work Instructions. ISOQualitas.PLM standardizes the quality management process. It is up to 80% more efficient than spreadsheets and fully compliant with IATF16949. Each member of the quality team can work simultaneously at their own task in the office or remotely. So that users and managers can stay on top of the latest information and focus on their priorities, tasks are displayed on progress charts. All documents are consistent, eliminating the most common audit non-compliance issue. Each user has their own role, so that information and document approval can be controlled.

For more than three decades, Helix QAC has established itself as a reliable static code analyzer specifically designed for C and C++ programming languages. Renowned for its thoroughness and precision, Helix QAC has become the go-to choice in highly regulated and safety-sensitive sectors that must adhere to strict compliance standards. This often entails ensuring alignment with coding standards like MISRA and AUTOSAR, as well as functional safety regulations such as ISO 26262. The tool boasts TÜV-SÜD certification for functional safety compliance, encompassing standards like IEC 61508, ISO 26262, EN 50128, IEC 60880, and IEC 62304. Furthermore, it holds ISO 9001 | TickIT plus Foundation Level certification, a widely recognized standard that guarantees not only the fulfillment of requirements but their surpassing as well. By allowing users to prioritize coding issues according to risk severity, Helix QAC enables efficient targeting of critical defects through various tools, including filters, suppressions, and baselines, enhancing overall code quality and safety. This commitment to excellence solidifies Helix QAC's reputation as an essential asset in the development process.

RAM Commander Enterprise Collaboration Edition (RAM Commander ECE) stands as the newest development in the RAM Commander lineup. Already embraced by leading aviation original equipment manufacturers (OEMs), RAM Commander ECE tackles the integration of Safety Assessment and Safety Certification through an array of distinctive features tailored for Integrated Safety Teams and design engineers. This innovative software is essential for achieving fail-safe designs across various industries, including Aerospace, Railway, Communication, and Energy. Distinctively, it is the sole off-the-shelf software capable of integrating Safety Analysis at the level of Aircraft or System-of-Systems. Furthermore, RAM Commander ECE adeptly transforms the Model-Based Design methodology into Fault Tree Analysis, which is crucial for Aircraft Type Certification, while also ensuring the definition, verification, and fulfillment of Safety Requirements for intricate System-of-Systems. With its advanced capabilities, RAM Commander ECE positions itself as a pivotal tool in the realm of safety engineering.

Eliminate expensive redesigns and setbacks that arise from discovering design issues late in the development cycle. Tackle the difficulties associated with handling and merging large quantities of data effectively. Guarantee the reliability and efficiency of intricate electronic systems. Minimize the lengthy RAMS analyses that can disrupt project schedules. Ensure a smooth integration of RAMS analysis tools with current CAD software. Obtain straightforward, actionable insights to facilitate better decision-making and enhance overall project outcomes. Emphasizing these strategies will foster a more efficient and streamlined development process.

Create your own templates or use the built-in templates to meet your needs. Your FMEA Worksheets and Dashboards can be completely customized to meet your specific needs! FMEA Process Control has reached a new level! Relyence's innovative Action Library and its powerful and customizable FMEA Workflow and Approvals and Notifications features help achieve the goal of living document FMEAs that are closed-loop. Relyence FMEA offers a wide range of powerful features that make it a top-of-the-line analysis solution. Relyence FMEA features are unmatched. They include role-based permissions and access control capabilities, as well as revision control. Relyence FMEA was designed with team concepts in the forefront. It allows you to access your analyses anywhere, anytime, and on any device, including mobile devices. Relyence FMEA is all about collaboration and connectivity.

Document Management Software facilitates the automation of various office tasks, enhances collaboration, streamlines document flow, and improves business processes. It also organizes quality control measures for both incoming and outgoing goods, which significantly reduces inspection times and minimizes costs. Furthermore, it offers comprehensive preventive maintenance management for equipment, ensuring optimal functionality. The tool allows for the meticulous documentation of meeting minutes and tracking of assigned tasks, while also supporting corrective actions, 8D methodologies, GAP Analysis, Kaizen proposals, FMEA, and Ishikawa diagrams. Additionally, it aids in the management of job descriptions, personnel records, announcements, suggestions, and complaints. Standardization of audit checklists and the documentation of conducted system audits, including 5S inspections, are also well-supported. Moreover, the software provides functionalities for the creation and management of Material Safety Data Sheets (MSDSs), ensuring compliance and safety across business operations. Ultimately, this comprehensive solution is designed to enhance efficiency and organization in all aspects of document management.

Streamline the creation and modification of FMEA, Process Flow Diagrams, and Control Plans like never before. The FMEA methodology can be quite intricate, but with FMEA Studio's automated features, you can significantly reduce the likelihood of errors. It offers user-friendly functionalities that make sharing documents with others a breeze. FMEA Studio accommodates various risk indices, including RPN, SOD, and CN, along with their respective evaluation techniques. You have the capability to assess FMEA risks through both 2D and 3D risk matrices, enhancing your analysis. Ranking parameters such as Severity, Occurrence, or Detection levels is made simpler and quicker with intuitive ranking tables that can be tailored to your specific requirements. Additionally, FMEA Studio provides a structural tree for visualizing structure, function, and failure analyses. Accessing editing tools is straightforward through a convenient right-click menu, ensuring an efficient workflow throughout the entire process. With these features, FMEA Studio not only enhances productivity but also promotes collaboration among team members for improved outcomes.

Focus BIS offers a comprehensive array of cloud-based management solutions designed to satisfy the demands of quality, safety, and environmental standards. Grounded in the principles of International Standards 9001, 45001, and 14001, their services deliver exceptional value. Specializing in Integrated Management Systems (IMS), Focus BIS focuses on ISO9001 for Quality Management, ISO45001 for Occupational Health and Safety, and ISO14001 for Environmental Management. Furthermore, they possess expertise in specialized accreditation programs, such as the Accredited Service Provider Level 1 for electrical companies involved in distribution network services and mining operations. As organizations face greater regulatory pressures, particularly when expanding their services, the integration of operational and management systems becomes vital for navigating both accreditation and compliance efficiently. This strategic approach not only streamlines processes but also enhances overall organizational performance.

The SCIO™ software by PLATO has gained significant traction among professionals and facilitators alike. For those in the engineering sector, the web-based PLATO e1ns is highly recommended for its user-friendly design, making it accessible for all team members. This platform integrates the core functionalities of SCIO™ effectively. PLATO e1ns serves as a pivotal tool for enhancing the product development process (PDP), particularly during its initial phases where crucial decisions regarding cost and risk management are made. With e1ns, PLATO offers a solution that focuses on the foundational elements of PDP for optimal efficiency. The advanced database capabilities of SCIO™-FMEA meet the essential requirements for knowledge management, support multiple users, and cater to various languages. Furthermore, the SCIO™-Matrix provides a rapid approach to system analysis, enabling the transformation of customer needs into product features with effective execution. This comprehensive tool ensures meticulous planning and documentation of each process step, all of which are securely stored in the SCIO™ database, ready for future reference and use. In this way, PLATO empowers teams to streamline their workflows and enhance productivity throughout the development cycle.

AutoDCP facilitates the linking of individual projects or specific operations into a unified composite project, which proves beneficial for integrating purchased components, various parts, or generic processes alongside part-specific details. This feature ensures that any changes in the foundational data automatically reflect in the composite projects. Furthermore, AutoDCP stands out as the quickest and most economical solution for sustaining an interconnected Process Flow Diagram, FMEA, and Control Plan. The inclusion of Risk Profiles streamlines the FMEA creation process, making it both efficient and rapid. Its user-friendly drag-and-drop interface simplifies the FMEA development experience, allowing users to navigate the system with ease. Additionally, AutoDCP is equipped with numerous features that significantly enhance productivity, demonstrating that the process of creating and updating FMEAs and Control Plans can be accomplished in a fraction of the time it would traditionally require. Ultimately, these advancements help teams focus more on analysis and less on administrative tasks.

In today's complex world, we are witnessing constant change and rapid advancements in technology. The pace of new developments is swift, and the expectations for quality and safety are becoming increasingly stringent. In this environment, digitisation requires agility and speed. With Icologiq Elements, your organization can effortlessly meet all local and international standards and regulations, no matter where you are located globally. Our approach centers around a strong partnership between your team and ours, ensuring seamless collaboration. We don’t just provide software; we walk you through the implementation process from the outset. Leveraging our vast experience with successful businesses across various sectors, we offer a ready-to-use package that encompasses all essential functionalities, which can be tailored to create a customized solution. Additionally, you have the flexibility to design the system according to your preferences and incorporate additional features as needed. This adaptability allows your organization to stay ahead in a rapidly evolving landscape.

Quality Planning Studio's FMEA software combines essential quality tools while guaranteeing compliance with key process flow stages. This all-in-one software solution facilitates the planning, documentation, and oversight of vital quality standards. For manufacturers around the globe, FMEA has become a crucial element of ongoing improvement initiatives. The interconnectedness of Process Flows, FMEA, control plans, and SPC is pivotal to fostering quality enhancement. Through the FMEA process, there is a continuous drive to refine products, processes, or detection methods. Engineers engaged in the FMEA process receive ongoing insights from SPC outcomes observed on the shop floor. The QPS database effectively centralizes all information, maintaining the traceability and integrity of your Process Flow, FMEA, and Control Plan data across various manufacturing locations. Additionally, QPS can integrate with our SPC software, DataMetrics, which streamlines operations by minimizing redundancy while enabling effective monitoring of characteristic capabilities derived from the Control Plan. This seamless integration ultimately enhances overall operational efficiency and quality assurance.

QAD EQMS (Enterprise Quality Management System) is a fully integrated enterprise quality management system that provides timely visibility into manufacturing and quality-related issues across the enterprise. It facilitates a preventative approach that helps to build quality into the process from the product design phase.

Comprehensive software for reliability and safety tailored for professionals. It facilitates reliability block diagram analysis, fault tree evaluations, and common cause importance assessments. The software also conducts event tree analyses across various risk categories and employs Markov analysis for multi-phase modeling. Users can connect hazard logs and requirements to RBD or fault tree verification models seamlessly. Additionally, it supports multiple industry standards for system analysis, including ARP 4761, IEC 61508, and ISO 26262. It enables the prediction of reliability for both electronic and mechanical components utilizing frameworks such as MIL-217, Quanterion 217 Plus, and SN29500, among others. FMEA and FMECA assessments adhere to standards like MIL-STD-1629A and SAE J1739, ensuring comprehensive risk evaluation. Furthermore, the software integrates smoothly with Requirements Management tools, such as Jama Connect®. Since its inception in the 1980s, our software has evolved continuously, establishing itself as the benchmark for professionals in safety and reliability fields. Its ongoing development ensures that users have access to the latest features and compliance with emerging industry requirements.

QUALIPRO is a comprehensive management software designed for quality, environmental, occupational health and safety, and food safety management. It offers assistance, research, and consulting services in quality, environmental issues, workplace health and safety, and HACCP standards. The software also provides training and awareness programs related to quality, environment, health and safety at work, food safety, and auditing techniques. Its customizable nature and specialized modules allow QUALIPRO to meet the specific needs of the Pharmaceutical and medical device industries effectively. QUALIPRO adheres to the principles of “Good Manufacturing Practices (GMP)” and complies with ISO13485 standards. Additionally, it aligns with key international standards such as ISO 9001, EN 9100, ISO IATF 16949, ISO 14001, ISO 17025, ISO 15189, ISO 22000, IFS, ISO 27001, and ISO 45001. As a state-of-the-art and modular software solution, QUALIPRO serves as a powerful tool for managing Quality, QSE, SHEQ, and SHE systems. Its versatility makes it an essential resource for organizations striving for excellence in quality and safety management.

Our SHEQX (Health, Safety, Environment and Quality Management) solution aggregates SHEQ data and manages analysis and reports effectively. This ensures effective compliance and a more robust approach to corporate sustainability. Our modules Our SHEQX (Health, Safety, Environment and Quality) management solution aggregates SHEQ data in a single, auditable database and manages the analysis and reporting effectively, ensuring adequate compliance and a more robust approach to corporate sustainability. Our suite of modules will assist in driving compliance with international standards and guidelines such as ISO 9001, ISO 14001, ISO 45001, ISO 31000, COSO, HACCP and more. SHEQX is an integrated management system with links between all modules within our solution. XGRC Software aggregates ESG data in a single, auditable framework that drives compliance ® and corporate sustainability. The solution is pre-configured with base ESG matrices like SASB & GRI standards and other models like the 6 capitals.

Q-Med Database is ideal for small businesses striving for ISO 13485 compliance. The Q-Med Database is an ISO 13485 compliant database to efficiently manage corrective and preventive actions, nonconformances, internal audit schedules and findings, safety improvement, supplier corrective actions, continual improvement projects. Compile and analyze Customer Survey results. Document QMS review meetings and results. CFR21 Part 11 compliant Cloud based or locally installed options are available. The

Isolocity is the front-to-back solution for ISO 9001 and GMP cannabis compliance in the industry. Our software seamlessly combines the principles of GMP, ISO and the management and documentation for your production. Isolocity's compliance software was designed with GMP principles. Each module is essential for improving safety and yield in your facility, allowing you to easily become certified. Isolocity automates labour-intensive processes to make ISO 9001:2015 compliance easy. Isolocity's QMS software can help you improve consistency in production as well as guide you through your ISO 9001 certification. Isolocity's risk management module also includes HACCP planning and PFMEA. You can easily plan, initiate, prioritize, and track actions to minimize failures and hazards in your production. Our tablet-friendly solution allows you to manage inspections and provide the quality manager with real-time reports. Isolocity allows for full traceability from customer through supplier.

OpenText™ Information Management solutions empower organizations in the life sciences sector to harness data and content insights, enhancing their decision-making and speeding up product development. These tools enable seamless integration, management, and secure sharing of information among individuals, systems, and devices. By utilizing information assets effectively from research and development through to commercialization, organizations can benefit from adaptable cloud-native software that operates in any environment. OpenText for life sciences significantly accelerates the discovery process, facilitating the extraction of actionable insights that foster innovation in the pipeline. Users can convert research papers into electronic lab notebooks through intelligent capture, and uncover valuable insights using text mining techniques. Moreover, the platform allows for the extraction of knowledge hidden within unstructured text of clinical trial reports, study protocols, and findings related to clinical safety and efficiency. It also offers methods to intelligently analyze, categorize, and extract information from clinical trial documents, ultimately minimizing the risk of expensive delays and interruptions in the development process. By effectively utilizing these advanced capabilities, life sciences organizations can significantly enhance their operational efficiency and drive forward their research initiatives.

QMS allows companies to eliminate paper-based quality control processes while still adhering to regulatory standards and compliance. QMS not only improves operational efficiency, but also increases compliance to established quality standards. QMS combines all your quality processes into one place. It integrates related actions and processes to facilitate better analysis and process improvement. QMS has been vetted by the USFDA and European Regulatory Auditors and found to be compliant with CFR 21 Part 11 guidelines. Benefits All related processes can be managed from a single platform Reduce expensive mistakes Evidence to support educated decision making Credibility improvement Improved customer satisfaction

Quarta EVO is an online Quality Management software designed for Quality Assurance and Compliance, leveraging a robust workflow engine. This platform enables the digitization of quality systems and allows users to monitor processes seamlessly from any location, utilizing an integrated internal dashboard and key performance indicators (KPIs). It serves as an effective QMS solution to enhance and oversee the performance of Quality and Safety Management Systems within organizations. Built on a powerful workflow engine, it merges extensive functionality with modern web-based architectures and technologies, all aimed at facilitating collaboration across different plants and evaluating process performance. The Quarta suite stands out for its user-friendly, fluid, and intuitive interface, capable of gathering real-time data, performing analysis, organizing information, and automatically generating a series of indicators to maintain comprehensive oversight of the entire Quality System. As a result, organizations can expect improved efficiency and enhanced compliance through the use of this innovative software solution.

ShopXpert is a robust and fully integrated manufacturing software solution that enhances your entire manufacturing process by reducing data entry and boosting productivity levels. By automating various tasks, it effectively minimizes manual processes and inefficiencies that can hinder job shop performance. The software encompasses a wide array of modules, including standard modules, a supplier portal, outsource management, job tracking, an employee portal, vending capabilities, a costing tool, customizable forms, task management, workstations, training notes, an academy, a time clock, in-app messaging, storage solutions, and QR code functionalities. Each of these modules is designed to offer features such as dashboard access, efficient customer and supplier management, document storage capabilities, customizable forms, task scheduling, employee time tracking, and real-time communication with suppliers. Additionally, it empowers employees to manage their jobs seamlessly from tablets or mobile devices, significantly decreasing the reliance on traditional desktop workstations. This flexibility not only enhances operational efficiency but also fosters a more agile work environment.

Polyspace Code Prover serves as a static analysis tool aimed at ensuring that critical runtime errors are absent in C and C++ code without the need for execution. By employing formal methods, it examines every code path and possible input scenario to detect issues such as overflows, division by zero, and out-of-bounds accesses. The tool offers valuable insights into the ranges of variables and highlights unreachable code, which aids developers in enhancing software performance and maintaining quality. Additionally, Polyspace Code Prover adheres to safety standards including IEC 61508, ISO 26262, and DO-178C, making it an excellent choice for industries that demand strict software certification. Its comprehensive analysis capabilities enable teams to deliver reliable and robust software solutions.

When it comes to inspections, quality assurance, and safety management, having robust software is essential. When you factor in the sheer volume of inspections performed throughout the lifespan of numerous serial-numbered tools and equipment, the necessity for specialized software that can tackle these complexities becomes evident; it has the potential to save significant time and cut costs. At FTQ360, we recognize the difficulties involved in managing oil and gas inspections and tests, particularly in accurately documenting every detail, as the stakes involve human lives, environmental protection, and substantial financial resources. It is crucial to maintain the highest operational standards and ensure that your global inspection teams are held accountable on a daily basis. Additionally, demonstrating compliance to regulators, customers, and legal entities is a challenging endeavor. However, if you are committed to finding a global compliance platform that optimizes your quality efforts and effectively manages safety-critical inspections, we are here to assist you in achieving those goals. Our solutions are designed to provide the support you need in navigating these complex requirements.

FreePoint Technologies' ShiftWorx provides a ‘holistic’ shopfloor management platform that when applied in whole or in succession affords manufacturers a production optimization solution backed by Toyota Production System (TPS) consulting expertise. ▪ Fully customized modular suite of products. ▪ Toyota Production System (TPS) expertise ▪ Measures and monitors critical production areas. ▪ Managed Services included. ▪ Cloud-connects equipment of any age, type or brand. ShiftWorx is a unique grouping of modules that provide an end-to-end solution for continuous improvement across the production floor. ▪ Production Management - Real-time information on machine performance, jobs, and operator workforce. ▪ Performance Analysis - Metrics at the machine, line or plant for historical, situational and predictive insights. ▪ Quality & Compliance - Benchmarking, standards and procedures to meet audit and compliance regulations. ▪ Team Member Development & Performance - Operators have better tools for creating value added work. Measure, Analyze, and Improve with ShiftWorx! Contact us for a complimentary consultation from our TPS experts! Schedule a software demo specific to your Industry today!

qmsWrapper is an interconnected Quality Management Software for startups and small businesses. It helps all companies that want to increase productivity with ISO 9001:2015 and MedDev creators to easily achieve and manage ISO 13485:2016 and 21 CFR 820. Best For 1. For companies who need guidance to implement and adopt validated QMS. 2. For companies who want to automate their quality management and go beyond a paper-based system.

Limsophy BPM offers an effective solution for quality management needs, emphasizing a streamlined approach to document management that ensures sustained high quality with minimal effort. This platform facilitates the creation and oversight of quality management documents while also integrating essential management functionalities, including audit planning, risk assessment, target management, and ongoing improvement initiatives. Recognized as a standardized information management system for business process management, Limsophy BPM is utilized daily by over 10,000 users across various industries. The software allows users to easily access their processes and documents through a web browser, enabling them to contribute valuable insights to the quality management system. With a unified database generating all links, the process management capabilities of Limsophy BPM guarantee uniformity in flow charts, process documentation, tools, and manuals, fostering a collaborative environment for continuous quality enhancement. This cohesive system not only simplifies management tasks but also promotes a culture of accountability and transparency within organizations.

Reva QMS is a software-driven Quality Management System tailored to assist organizations in the collection, organization, management, and reporting of essential business documents while ensuring alignment with pertinent industry regulations, standards, and laws. This solution is specifically crafted for sectors that are heavily regulated, enabling organizations to automate and enhance their previously manual processes, thus promoting greater efficiency and adherence to regulatory requirements. With a robust suite of built-in functions and features, Reva QMS empowers organizations in regulated industries to attain improved operational visibility and meet compliance obligations with various policies, industry standards, and best practices. Its user-friendly browser interface simplifies the management of critical business processes, making it accessible for users to navigate effortlessly. Additionally, the system's design supports seamless integration with existing workflows, further enhancing productivity across the organization.

The Intact Platform, a cloud-based and on-premise Enterprise Resource Planning solution (ERP), is the best for audits, assessments certification, accreditation, and other standards. It is more than any other audit collection tool on the market. It offers a complete solution that helps you manage communications and business goals as well as personnel. Intact Platform is unrivaled in functionality and features an end-to-end modular workflow that is easily scaleable. 34% efficiency increase on average (upto 60+%) Unmatched modularity, flexibility and scalability All standards and audit services Digital workflow - no need for paper Remote and on-site auditing Non-conformities and corrective actions Planning and risk-based auditing Communication with clients is easy Reporting and business intelligence (BI). Management and central data hub (incl. Audit trail complete Innovation never stops

DataLyzer Gage management software has been on the market for 40 years and is a complete webbased solution to calibrate gages and MSA research. It is fully integrated into our quality suite, which includes FMEA and SPC as well as OEE. It includes the following features: - Calibration of gages - Checking in and out of gages - Gage R&R and Kappa studies - Printing of calibration stickers.

XbarR, XbarS, Individuals, n, p, u, and np charts should be regularly updated after their initial creation, while also ensuring that any outliers are identified and displayed independently, so they do not interfere with the established control limits. Additional tools include histograms, capability analysis (Cpk), scatter plots with regression fitting, Pareto charts, dot plots, box plots, multiple regression analysis, hypothesis testing, confidence intervals, and calculations for sample sizes. Furthermore, it is essential to conduct measurement system analysis (Gage R&R) applicable to both quantitative and binomial data, along with creating cause and effect diagrams, main effects plots, cusum charts, product capability assessments, FMEA, and distribution calculators to enhance data-driven decision-making processes. Each of these analytical methods contributes to a comprehensive understanding of the data and its implications for quality control and improvement initiatives.