Alternatives to orgavision

Epsilon3 is the leading AI-powered procedure and resource management tool designed for teams building, testing, and operating advanced products and systems. ✔ Save Time & Money Avoid costly delays, mistakes, and inefficiencies by automatically tracking procedures and resources. ✔ Prevent Failures Ensure the right step is completed at the right time with conditional logic and built-in revision control. ✔ Optimize Collaboration Real-time progress updates and role-based sign-offs keep your stakeholders on the same page. ✔ Continuously Improve Advanced data analytics and automated reporting enable rapid iteration and data-driven decisions. Epsilon3 is trusted by industry leaders like NASA, Blue Origin, Firefly Aerospace, Sierra Space, Redwire, Shift4, AeroVironment, Commonwealth Fusion Systems, and other commercial and government organizations.

Adaptive Compliance Engine® (ACE®) is a highly configurable, workflow based eQMS/eDMS and more that can adapt to any business process, allowing for real-time tracking, management, and reporting of all compliance, quality, and operational activities. With ACE®, you will minimize the administrative hassles and maximize ROI with productivity gains from day one – all while 21 CFR Part 11 compliant. Our one-stop software includes: -Office 365 Integration -Inspection Management -Document Management -Risk Management -Product Lifecycle Management -Learning Management -Audit Management -Quality Events -Paperless Validation -Electronic Signatures (21 CFR Part 11 Compliant) -Endless Workflow Configurations -And so much more! Empower all levels of your organization with intuitive user interfaces, easily search for all your documents and records, and transform your data into actionable intelligence with advanced analytics all on a single platform. ACE comes with everything you need, all included at one price. Every application is included, no more a la carte pricing. No more nickel and diming. One software, endless solutions.

QBench allows you to keep track of all your samples and where they are located in the workflow using a single system. QBench eliminates the need for spreadsheets, shared folders in the network, and paper-based tracking systems. You can view hundreds of PDF reports/COAs before publishing or emailing. You can generate barcodes and create labels that you can customize for your samples. Compatible with standard printers and scanners. QBench's billing module allows you to create and send invoices right from the system. You can see counts and latencies for different data types in QBench. This includes metrics like turnaround time, sample counts per test, sample delay, and many others. QBench makes it easy for you to gather the data your lab needs for the assays you perform.

Sofvie is the only Operations Performance Platform built for the unique needs of today’s most demanding mining operations. Our goal is to help leaders at the forefront of the mining industry create safer work environments, happier engaged teams and more rewarding work cultures to unlock new levels of performance. Sofvie gives your teams the platform that helps unlock new levels of safe production and create better visibility to and from the face. Sofvie will help you create an environment where workers feel safe, supported, included and informed, driving increased engagement and empowering everyone to operate at their best. Our progressive web application functions on all modern devices, operating systems, and browsers, and has been designed for ease of use, resulting in a rich experience and quick adoption. Reduce risk to property, equipment, and people. Closes the circle of communication, reducing the gaps between teams. Identifies health and safety trends and facilitates predictive models.

Simplify compliance management and get everyone on board with your EHSQ goals! SafetyAmp is a cloud-based, mobile-friendly, cloud-based software that increases engagement, reduces risk, connects your workforce, and improves EHSQ workflows. SafetyAmp is the modern, configurable EHSQ software you've been searching for. It's trusted across industries by today’s workforce.

The [FP]-LIMS modules rely on a powerful SQL database solution. These modules allow for quick queries and data processing. We guarantee maximum user friendliness. Our job server is the central element of automation, which executes event- and time-controlled tasks. To monitor limit values and send an alarm message (email, message on monitor, etc.) automatically. When they are exceeded. Modern LIMS software, including modules such as inspection planning, workflow management, and analysis management, can help you design your quality management system in the most efficient way. This will make your production processes more efficient.

SAP Business ByDesign is an affordable, easy-to-use enterprise resource planning system (ERP) specifically designed for fast-growing small to mid-market businesses and subsidiaries of larger companies. From financials and inventory to customer relationship management and human resources, SAP Business ByDesign integrates all major aspects of your business for end-to-end visibility, added efficiency, and improved operational control. By serving as the nerve-center for your business, with all data flowing into a single, centralized system, SAP Business ByDesign enables real-time data access for faster, complete, more nimble decision-making. SAP Business ByDesign comes with workflows and best practices that help your business run operations more efficiently from Day 1. It also scales with your business, so you don’t have to change systems as you grow. Some of the key features of SAP Business ByDesign: Integrated system architecture that manages all your company dataSAP Business ByDesign Complete operational visibility and control End-to-end business process automation Precise real-time reporting and analytics Customization for business and industry-specific requirements Secure data access anytime, anywhere

Our namesake product, Minitab Statistical Software, leads the way in data analysis with the power to visualize, analyze and harness your data to gain insights and solve your toughest challenges. Access trusted, proven and modern analytics combined with dynamic visualizations to empower you and your decisions. The latest version of Minitab Statistical Software includes access to Minitab on the cloud so you can analyze from anywhere, and Graph Builder, our new interactive tool to instantly create multiple graph options at once. Minitab offers modules for Predictive Analytics and Healthcare to boost your analytics even further. Available in 8 languages: English, Chinese, French, German, Japanese, Korean, Spanish, and Portuguese. For 50 years, Minitab has helped thousands of companies and institutions spot trends, solve problems, and discover valuable insights in their data through our comprehensive, best-in-class suite of data analysis and process improvement tools.

Intellect's QMS software has been proven to improve quality operations and reduce overall quality cost by up to 40%. Our apps were designed by certified quality professionals and can be easily customized with our no-code platform or drag-and-drop technology. Remote access for your team, mobile apps, dynamic workflows, analytics, reporting, and remote access are all possible with this modern and simple solution. Apps include Document Control and Employee Training, Audit Management CAPA, Nonconformance, as well as other useful features.

icmInspector automates control, review, and audit processes. It includes a central component responsible for administration and management, and a mobile app for Android. Improvement of the quality of the organization through the use of modern inspection, control, and interial audit procedures that enable the detection of irregular or undesirable situations in a dispersed, real-time manner. By replacing paper versions with electronic versions, you can reduce operating costs and minimize time spent on material preparation and distribution. Tools that enable fast data collection, protect against omissions and offer the possibility of scheduling work can increase the efficiency of those who are responsible for audits and controls. Eliminate fraud, abuses, and errors in the control process by recording metadata about data collection and enforcing only logically permissible answers.

Trevally from ManualMaster is a comprehensive QHSE platform designed to cover the entire PDCA loop in a single web or on-premises solution. It provides controlled document and version management with audit trails, process mapping, risk and standard controls, as well as quality assurance registrations and smart web forms. Additional modules manage incidents, complaints, audits, deviations, tasks, and actions, all displayed in role-based dashboards with real-time KPIs, reports, and graphs. With ISO-27001 hosting, backups, single sign-on, two-factor authentication, and granular user permissions, Trevally ensures data security while supporting multi-language interfaces, digital signatures, and mobile access for enhanced user adoption.

CAQ.Net software solutions are in action all around the globe wherever it is important to ensure the quality, safety, and functionality of products and services. Whether strategic quality management or operational quality assurance – thanks to its high degree of automation and uniform data structure, CAQ.Net facilitates effective process management, proactive failure prevention, and a company-wide quality mindset.

Virje meets the standards set forth by 21 CFR Part 11, 21 CFR Part 820, and ISO 13485. If you're feeling daunted by the complexities of Part 11 software validation, rest assured that help is just a click away, no matter where you are or when you need it. By eliminating paperwork, cutting costs, and enhancing productivity through automation and unified collaboration, it becomes an ideal solution for small to medium-sized enterprises. Designed specifically for medical device quality management, this system is constructed to be adaptable to your unique workflows and processes, ensuring you don’t have to make any sacrifices. It features configurable change order approvals that can be tailored by employee role and document type, along with timely notifications sent to accountable team members throughout every phase of the change process. Users can assign material dispositions for specific documents, gain easy access to both released and archived versions, and quickly view the history of document changes. Additionally, it tracks where-used locations and the distribution of hard copies, while also providing reminders for periodic document reviews to ensure compliance and efficiency remain top priorities. This comprehensive approach not only streamlines quality management but also empowers organizations to maintain rigorous standards effortlessly.

Utilize online document creation and management to eliminate the chaos of lost printed materials and improve organization significantly. Centralize all relevant information, making it straightforward to track and resolve any discrepancies. Establish, gather, and evaluate key performance indicators using comparative charts to enhance your decision-making process. Strategically develop and execute plans to tackle risks and seize opportunities in an efficient and monitored manner. Transition away from traditional spreadsheets and paper files. Benefit from cloud-based file management that provides 24/7 accessibility from any device or location. Streamline the process of document creation, review, and approval to increase efficiency. Control access permissions and receive automatic alerts regarding document modifications and expiration dates. Always ensure that the latest versions of files are stored in Genebra, preventing time wasted sifting through countless spreadsheets and ensuring that revisions of your documents are never lost. Embrace a more organized approach to document management for better collaboration and productivity.

A unified platform for governance, risk management, and compliance. RISMA's GRC solution provides you and your team with a comprehensive overview, facilitating the management and documentation of your compliance, risk management, and control activities. The platform guides you through the necessary processes, ensuring that all participants only need familiarity with a single system, which boosts overall efficiency. Across various industries, adhering to regulations and standards is imperative and requires meticulous documentation. For many organizations, this can become an all-encompassing task. With the intricacies of legislation and a multitude of complex requirements, garnering support from within the organization can often prove challenging. As a result, navigating compliance can be quite complicated. Nevertheless, RISMA's innovative solution simplifies this process, allowing you to concentrate exclusively on your areas of expertise while ensuring compliance is managed effectively. This way, you can enhance your focus on what truly matters to your organization.

With mindmaxx, you can effectively manage the overwhelming array of your files, tasks, communications, reports, and schedules. This platform serves as a comprehensive library, communication hub, and reminder system all merged into one. An especially valuable feature offered by mindmaxx is its automatic update service, ensuring that any legal changes are promptly addressed by the mindmaxx team who will revise and refresh the necessary documents. You will receive the updated documents automatically and will be kept informed about these changes, along with practical application advice. However, high-quality management involves more than simply adhering to legal standards; it requires recognizing and capitalizing on opportunities, setting clear objectives, and taking proactive steps to reach them, which is crucial for success. This proactive mindset is increasingly vital in today's professional landscape, and mindmaxx provides robust support for you and your team in navigating this journey. All team members can conveniently access essential documents from a centralized platform through mindmaxx, enhancing collaboration and efficiency. By fostering such an organized environment, mindmaxx empowers users to thrive in their professional endeavors.

The Audit Manager software facilitates comprehensive quality management by enabling the digital oversight of audits, quality controls, and testing throughout all stages, including planning, checklist creation, evidence collection, field surveys, and the management of nonconformities. Users can easily access the calendar to schedule audits while attaching essential details such as the subject, checklist, lead auditor, co-auditor, and participants. Both internal and external personnel can receive timely email invitations and view the audit schedule directly through the application. After completing the inspection, users can generate audit reports in PDF or Excel formats and share them instantly with company management or relevant stakeholders via mobile. All minutes are neatly archived and accessible, ensuring that they can be seamlessly integrated into the document repositories utilized by the organization, enhancing overall efficiency and accountability in the audit process. This streamlined approach not only saves time but also improves communication among all parties involved.

InstantGMP™, which replaces multiple software and/or paper-based solutions for managing your manufacturing and compliance needs, could be the key to unlocking your business's full potential. With a single, affordable software solution, you can easily increase production uptime, improve batch quality, and meet all FDA compliance requirements. InstantGMP™, which can be used individually or together depending on your business needs, delivers comprehensive, integrated software solutions that ensure quality, consistency, and GMP compliance. We will help you choose the right solution for your business today and tomorrow. You can organize, manage, and document batches electronically while promoting good manufacturing practices. Inventory Management Software that meets Part 11 requirements and GMP requirements. A complete quality system with templates, SOPs and guided workflows that is ideal for virtual biotech.

Implementing Systematic Safety Management, Compliance Monitoring, and Quality Management is essential not just for meeting legal obligations as commercial air operators, but also for enhancing organizational efficiency, reducing costs, and ultimately boosting profitability. Relying on standard software applications and manual processes for overseeing safety, compliance, and quality can lead to missed opportunities for substantial efficiency improvements that an electronic solution, such as Qperfect IAMS, can provide. Transitioning to a tailored digital approach can transform how these critical areas are managed, ensuring a more streamlined operation.

Streamline your COSHH Risk Assessments and Safety Data Sheets with ease. Our innovative software is designed to help you organize your chemical safety protocols while ensuring compliance. Just provide us with a list of the products in your inventory, and we’ll handle the rest, making Safety Data Sheet management effortless. We collaborate with you to develop tailored COSHH Risk Assessment templates that suit the specific needs of your organization. Through our online platform, you can generate chemical safety reports that can be easily shared with all team members across your business. Chemdoc is a chemical safety management tool that not only saves you valuable time but also reduces costs. By directly obtaining Safety Data Sheets from manufacturers on your behalf, Chemdoc empowers those responsible for chemical safety with the resources to create customized, compliant COSHH Risk Assessments, ensuring the well-being of your workforce while adhering to necessary regulations. This comprehensive solution aims to enhance safety and efficiency within your organization, allowing you to focus on what truly matters.

Managing Quality, Safety, and Environmental Management Systems may appear daunting and challenging to sustain. However, we are here to assist you, as we possess an in-depth understanding of the standards and have developed Toolbox to streamline your systems, ensure compliance, and enhance your business performance in the process. We firmly maintain that with the right approach, QHSE management systems can be straightforward and manageable; since they are grounded in robust business principles, implementing them leads to overall business improvement as well. This system serves as an organized workflow to manage, share, and oversee an organization’s files and documents effectively. By controlling your documents, you can save time, reduce effort and frustration, and minimize the risk to business continuity. The Toolkit features a workflow that accommodates both a version of a document that is still in development and a finalized version available for public access. Additionally, it retains previous versions and maintains a comprehensive audit log to track all changes. Team members have the ability to subscribe for updates, ensuring they stay informed about all modifications. Furthermore, this proactive approach not only simplifies document management but also fosters collaboration and transparency within the organization.

GenieTracker™ offers a robust, user-friendly, and web-based solution for tracking bugs and managing quality within enterprises. Built with contemporary internet and database technologies, it ensures optimal performance and reliability. The software is designed to work seamlessly across all major web browsers currently available, while also supporting older versions for continued usability. It boasts a variety of features that streamline the reporting and tracking of issues, allowing users to navigate through even extensive databases of hundreds or thousands of bugs with ease. Users can quickly access critical information directly from the Home page, ensuring efficiency in managing incidents. Additionally, the system provides a suite of statistical reports, giving managers immediate insights into the status of projects and products, as well as an overview of the entire development lifecycle. Each report comes with clear guidance on interpreting the displayed data, which enhances decision-making processes. Overall, GenieTracker™ combines advanced technology with user-centric design to support effective quality management in software development.

Transform your inefficient, paper-heavy management system into a streamlined, cost-effective digital solution. The Documentation module enables you to efficiently oversee the review, modification, approval, distribution, and accessibility of all your documents. Additionally, it allows you to track and manage issues arising from defects in your organization's products, services, or systems. You can categorize how your data will be reported by grouping problems based on your specific criteria such as regions, services, product categories, processes, and associated risks. Moreover, the software facilitates the creation of schedules for both Internal and supplier audits, ensuring responsibilities are assigned and linking findings to the corresponding planned audits. You can also establish a rolling schedule for calibration and maintenance tasks according to your specified frequency. All task records, along with any related attachments, are securely stored within the software. Furthermore, this module is offered at no additional cost, enhancing your operational efficiency without straining your budget.

CSols AqcTools™ v2.6 enables users to efficiently visualize Analytical Quality Control (AQC) charts for tracking laboratory performance, facilitates thorough, paperless investigations of control limit breaches, generates detailed reports, and significantly shortens the time required to evaluate and manage QC data. This tool is particularly advantageous for clients in sectors like water, environmental science, public health, and industrial labs engaged in chemical, clinical, and microbiological analyses. AqcTools offers a variety of ‘dynamic, interactive’ charts, ranging from standard ‘individual plotted AQC points’ to charts that can present batch or daily averages for both present and historical datasets. Furthermore, it allows users to create charts for specific analysts, aiding labs in their ongoing evaluation of analyst competence. Moreover, all pertinent information related to each individual data point, such as date, batch number, analyst, and instrument, can be accessed with just a single click, enhancing overall usability and efficiency. This means that users can have a comprehensive view of their data without unnecessary delays.

Document Control is a document management system that supports controlled processes and practices in creating, reviewing, correcting and issuing documents. The QMS QISS is an ISO-based QMS QISS Software System that automates corrective action processes in regulatory environments. Your own risk-based thinking. To reduce and mitigate your risk, centralize. Standardized workflows allow you to keep track of all changes within your organization. You will enjoy many additional benefits from a paperless document management system. Establish a culture of continuous improvement and make sure that each non-conformance is visible.

AcceleratorKMS empowers organizations to prevent incidents caused by information mishandling. It enables employees to access mobile-optimized content effortlessly. Regular updates and reviews of information are facilitated, ensuring that the content remains relevant and current. The platform simplifies the authoring process, allowing users to reduce costs effectively. It also helps monitor workflows to identify efficiencies, thereby cutting down the time and resources spent on onboarding new hires. This innovative solution creates a cohesive digital content environment that is user-friendly, aiming to simplify complex tasks. Our primary objective is to enhance the accessibility of information for front-line workers, contributing to safer operational practices. By providing immediate access to essential digital Standard Operating Procedures (SOPs), policies, and training materials via mobile devices, we significantly lower the risk of human errors. Furthermore, the standardization of all operational content not only mitigates information-related incidents but also simplifies usage through AI-enhanced procedure authoring. This approach minimizes the need for extensive administrative oversight and reduces management workload, as the standardization process leads to a decrease in the overall volume of operational content. In turn, organizations can focus more on their core activities, fostering a more efficient work environment.

isorobot serves as an advanced software solution for business management, effectively linking individuals, processes, technology, resources, and finances to align with your organizational objectives. Leveraging our expertise, we assist you in creating streamlined and scalable systems tailored to your enterprise. This performance management software focuses on achieving sustainable excellence by emphasizing innovation, quality, efficiency, and sustainability as its core principles. The solutions are grouped by fundamental business areas and organizational maturity, providing a solid foundation for growth and scalability. There is also an enterprise version available, designed for established businesses looking to expand right from the start. At the heart of the isorobot framework lies the integration of people, processes, technology, resources, and capital, forming a comprehensive model applicable to any organization. This universal framework promotes effective information sharing across various sectors, cultures, and stages of development, fostering collaboration and growth. By prioritizing these elements, isorobot empowers organizations to navigate their unique challenges and seize new opportunities.

Integral QA management and coverage will ensure that you have full visibility and quality coverage. All aspects of manual testing, exploratory testing, and test automation management are included in one central hub of information TEST CASE MANAGEMENT will increase efficiency and reduce the need to do the same job repeatedly. Write your test cases once and then use them again. TEST SETS and RUNS allow you to save time, test faster, and gain deeper testing insights. Cleanly organize your exploratory and scripted tests and execute them Requirement management will help you keep your team's attention. Identify goals and objectives, and track their fulfillment Confidently release products or update products using ISSUE STATUS management You can monitor each phase of the testing process and track real-time progress. SMART AND EASY DATA STRUCTURING makes it easy to find what you need and executes it easily. You can work more efficiently by combining PractiTest elements with your workflow More

AIMSCO eChecksheets™ (eCS) represent a modern, cloud-based approach to gathering a wide range of production, quality, visual, and process information in real time right at the point of use, offering immediate insight. These eCS can be rapidly designed and implemented at individual facilities or across several plants, accommodating various languages. With a comprehensive collection of industrial eCheckitems™ (eCI), eCS are overseen by designated users to facilitate data gathering and ongoing enhancement efforts. Not only can data be entered manually, but eCI can also be automatically filled by equipment interfaces (IoT) or enterprise systems utilizing standard web service connections. By utilizing the Microsoft Azure Cloud, AIMSCO Power Plant™ services enable seamless integration of eCS data with Microsoft Power BI® through tailored data models, allowing for sophisticated analytics and effective process visualization. This innovative solution significantly streamlines operations and enhances decision-making capabilities across the board.

High QA is a comprehensive software platform for managing quality in manufacturing, aimed at automating and optimizing quality processes throughout the entire production lifecycle. It features one-click ballooning for both 2D and 3D drawings, automatic extraction of GD&T and PMI data, and the creation of Bills of Characteristics (BOC) that utilize universal feature IDs, which greatly simplifies the planning and execution of inspections. Additionally, it encompasses all essential quality documentation processes, including First Article Inspection (FAI), Production Part Approval Process (PPAP), and Advanced Product Quality Planning (APQP), ensuring adherence to established industry standards. The High QA 360 solution further enhances operations by enabling real-time data collection and analysis from a variety of inspection tools, delivering actionable insights and timely alerts that support proactive measures. Moreover, its modular structure allows for easy integration with ERP, PLM, and MES systems via standard connectors and RESTful APIs, significantly improving collaboration throughout the supply chain. As a result, organizations can achieve greater efficiency and effectiveness in their quality management efforts.

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.

For a system to be effectively utilized, it must be easily accessible! Users should not have to endure long loading times or delays in search results. Instead, the goal is to swiftly and effortlessly access information or add records at any time and from any location! Wismatix QMS is designed to meet these needs. With years of expertise in auditing and implementing Quality Management Systems, we have crafted Wismatix QMS to ensure exceptional speed and reliability. Our commitment to customer service is unparalleled. You will receive comprehensive support while using our online quality management system, and should you decide to discontinue its use, we guarantee that your data will be provided to you for easy transfer to your own server. Moreover, we strive to maintain the highest standards of user satisfaction throughout your experience with us.

AQF is a sophisticated quality management software designed by experts in quality assurance. This comprehensive solution enables companies to completely abandon paper-based processes, facilitating seamless execution of all quality assurance activities. We provide a flexible, modular service that allows organizations to select a product tailored to their specific needs without incurring unnecessary expenses. The only essential module required for implementing additional features is the primary one. Not only does the AQF module enhance its own capabilities, but it also integrates well with any existing software or ERP systems your company may already have in place. You can easily create, manage, and share your internal controls, supplier audits, procedures, and documentation. Streamlining procedures among users is simplified, as it allows for the assignment of specific rights to regulate outgoing information. Additionally, it automates documentation requests to prevent any oversights. With the integration of Internet of Things (IoT) technology, you can effectively monitor and control environmental factors such as temperature and humidity, further enhancing your quality management processes. This holistic approach ensures that quality assurance is not only efficient but also adaptable to the evolving needs of your organization.

QSE SMART is a specialized software application for quality, safety, environmental, and risk management, tailored for small to mid-sized businesses and projects accommodating between 5 to 500 users. This application offers a robust framework that aligns with essential ISO standards such as ISO9001, ISO45001, and ISO14001, thereby streamlining the daily operations of your integrated QSE management system. By making ISO standards relevant to your business, QSE SMART enhances understanding and implementation. Built on a risk-based methodology in line with ISO 31000, it empowers organizations to gather and utilize critical data and metrics that align with their goals regarding quality, safety, environment, and risk management. This includes tracking objectives and targets, conducting management reviews, identifying risks and opportunities, managing non-conformities and improvements, performing audits and inspections, and addressing accidents, incidents, and hazards. Additionally, it covers corrective actions, equipment calibration, and the control of documented information, ensuring comprehensive oversight and continuous improvement in your organization's processes.

Walsh QA Inspector simplifies the monitoring and management of your comprehensive QA program. With just your tablet or smartphone, you can access all your checklists, covering locations, personnel, items, standards, and procedures. Data loses its value if it fails to narrate a story; therefore, our diverse reports offer numerous narratives, each delivering distinct insights and conclusions. These reports include performance evaluations, score assessments, deficiency frequencies, unfinished work, ATP scores, and a variety of others. You can easily filter the information by date, location, housekeeper, inspector, supervisor, or checklist. We facilitate the import of personnel names and emails from your facility, encompassing inspectors, accountable parties, informed parties, and administrators. Our user-friendly applications enable immediate use, often eliminating the need for any training. Inspections, rounds, and surveys can be conducted by anyone using their personal devices, enhancing accessibility and efficiency. Follow-up emails are automatically dispatched, and necessary escalations can be triggered as needed. Additionally, individuals will receive reminders about outstanding tasks and approaching deadlines, ensuring that nothing falls through the cracks. This comprehensive approach guarantees that your QA efforts are both effective and streamlined.

OpenText ALM Quality Center is a single-pane-of-glass for software quality management. It helps you implement rigorous and auditable lifecycle process and govern application lifecycle activities. Use the reusability and traceability of ALM tools, as well as their automation, to improve efficiency when developing, testing and maintaining applications. Automate the collection of results and gain real-time insight into application quality by eliminating time-consuming, error-prone manual processes. Standardize processes with templates and workflows built into ALM. Ensure compliance through detailed change tracking, a risk-based strategy and detailed change tracking. Integrate and use APIs to create a vendor-neutral, automated ecosystem for data consolidation throughout your application lifecycle. Choose the deployment option that best meets your needs for scalability and security.

StonemontQC stands out as the leading system for managing aggregate quality control and process information in the market today. This software is specifically tailored for manufacturers of crushed stone, sand, gravel, frac sand, lime, cement, and various other construction materials that necessitate meticulous particle size analysis and management of quality or composition data. With a plethora of analytical tools and reporting features, StonemontQC enables users to enhance consistency in their products, thereby meeting customer expectations more effectively. Furthermore, it complies with numerous state agency reporting standards, which helps eliminate redundant data entry and saves valuable time and resources. The software is versatile, offering desktop, server, enterprise, and hosted solutions that cater to both small operators and large-scale producers. Centralized management is a hallmark of the server, enterprise, and hosted versions, allowing for real-time analysis and reporting capabilities. Additionally, the automated functionalities include alerts via email for quality failures, alongside the ability to generate and distribute data analysis and reports on a daily, weekly, or monthly basis, ensuring that users are always informed about their quality metrics. Ultimately, StonemontQC not only streamlines operations but also significantly contributes to overall productivity and efficiency in the aggregate production process.

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

Ensuring uniform product quality and robust quality management procedures poses significant challenges in the current landscape of pharmaceutical manufacturing. Industries governed by strict regulations, including Pharmaceuticals, Biotechnology, and Life Sciences, must adhere to Good Manufacturing Practices (GMP) to comply with legal standards. Beyond merely fulfilling GMP obligations, it is essential to provide evidence of compliance. Relying on paper forms, isolated systems, or manual procedures to oversee, monitor, and document quality issues and responses fails to offer effective solutions for establishing cohesive and integrated quality management practices that align with industry standards. Consequently, organizations must seek more advanced and automated systems to enhance their quality assurance efforts and streamline compliance.

Mobile app is the complete solution to auditing and inspections. The most efficient way to raise your standards and improve your quality scores! Mobile inspections and audits can be conducted on any device. Even offline. Automatically generate PDF reports that are engaging, informative, and engaging for each inspection. Corrective actions close the loop. Our advanced analytics dashboard gives you unprecedented insight into your operations and optimizes your ROI.

Pro-Inspector is a powerful, enterprise-level platform for managing inspections and audits end-to-end. It supports over 2 million inspections annually across sectors like construction, oil & gas, food, insurance, and public safety. By replacing manual, paper-based methods with digital checklists, Pro-Inspector ensures inspections are accurate and consistent. The platform simplifies the entire inspection process with advanced tools for planning, scheduling, real-time data capture, offline access, remote approvals, and instant reporting. Highly customizable to fit complex workflows, it integrates smoothly with ERP systems, automates compliance monitoring, and enhances efficiency in safety, quality, and regulatory audits.

Document control made easy. You can create, review/approve and revise documents, as well as retire them. All transactions are recorded using e-signatures, timestamps, and stored in the Audit Trail. Audits from start-to-finish The SOLABS QM10 Audit APP allows you to track and document all aspects of your audits, from planning and preparation to closing. The SOLABS QM Essentials package offers advanced reporting capabilities and intuitive reporting. Trending and tracking are critical components of any quality management system. The dashboards and reports are easy-to-use, customizable, and can be shared in the most popular formats such as Excel, PowerPoint and PDF. You can share the reports and dashboards with anyone in your organization. In a matter of seconds, you can create, schedule, monitor, and assign training. Online assessments can be used to validate the learnings of your team. You can manage all aspects of training with the SOLABS QM Training section.

Lyons Quality Audit Tracking System® (LQATS) is a web-based solution that allows you to collect, analyze, and display quality audit results from suppliers and staff within a manufacturing company. LQATS collects real-time audit information from all over the world. Suppliers (shipment audits) Final audits by company auditors Distribution centers Plants for manufacturing LQATS allows for real-time entry, tracking and analysis of quality audit data from Distribution Centers and Supplier Plant locations. These features include: Smart controls to reduce user data entry and retrieval Tracking of Change History You can quickly search for data using many different query parameters Monitor global performance in real-time Fabric inspections Six-sigma analysis Disposition log Data presented in tabular and graphic formats, with output to Excel, PDF, or other formats.

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.

Enterprise software to improve business agility. objectiF RPM features include portfolio, requirements, test and risk management. UML/SysML diagrams allow you to visualize requirements, goals, and processes. You can also manage backlogs at different levels (from business use case, user story), plan taskmanagement with Kanban boards and run queries across multiple projects. This allows you to collaborate with distributed teams using one source of information. The software can be customized to meet your corporate needs. It is flexible, extensible, and integrable. It provides templates for agile and mixed project management, digitization programs, and projects following Scaled Agile Framework®, SAFe.