Alternatives to inblue QMS

Process Street is the Compliance Operations Platform built for teams that need to move fast without breaking standards. It combines document control, workflow automation, and AI-powered oversight in a single system so every policy is followed, every step is tracked, and every audit is effortless. Unlike legacy GRC tools or static SOP docs, Process Street turns compliance into a living system. Policies are documented in governed, version-controlled Pages. Those policies are executed through dynamic workflows with built-in task assignment, approvals, and forms. Every action is logged, monitored, and optimized in real time by Cora, our AI compliance agent. Used across industries like financial services, real estate, healthcare, and manufacturing, Process Street helps teams automate employee onboarding, streamline audits, manage policy updates, enforce vendor reviews, and run critical processes at scale. No code required. No micromanagement. Just proof that work gets done right, every time. Companies like Salesforce, Colliers, Drift, and Hartford Healthcare trust Process Street to eliminate busywork, improve operational visibility, and reduce compliance risk across the business. With native integrations, role-based access, audit trails, and ISO-aligned workflows, it is the platform that makes compliance a competitive advantage. From onboarding to audits, Process Street is how high-stakes teams enforce standards, automate execution, and prove compliance by default.

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.

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

QRA’s tools streamline engineering artifact generation, evaluation, and prediction, refocusing engineers from tedious work to critical path development. Our solutions automate the creation of risk-free project artifacts for high-stakes engineering. Engineers often spend excessive time on the mundane task of refining requirements, with quality metrics varying across industries. QVscribe, QRA's flagship product, streamlines this by automatically consolidating these metrics and applying them to your documentation, identifying risks, errors, and ambiguities. This efficiency allows engineers to focus on more complex challenges. To further simplify requirement authoring, QRA introduced a pioneering five-point scoring system that instills confidence in engineers. A perfect score confirms accurate structure and phrasing, while lower scores prompt corrective guidance. This feature not only refines current requirements but also reduces common errors and enhances authoring skills over time.

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.

integrum is a flexible, user-friendly, flexible, and comprehensive integrated management system that addresses Governance, Risk & compliance, Safety, Health, Environment, Quality Management System, Governance, Risk & Compliance, Quality Management System, Safety, Health, Environment, and Quality Management System. Over 1.5 million users worldwide use integrum to help them streamline their processes, reduce risk and accelerate their business growth. integrum offers pre-designed business processes that can be modified, used as-is or customized to meet your needs. Drag and drop functionality allows for easy configuration of any business process. Mobile apps (Apple and Android), which allow for the flexibility to complete any business process in the field in real time. We then use all the data generated by your team and create real-time business intelligence reports to provide insight into what is going on in the business. This allows the business to make quick, data-driven decisions and provides governance over the business.

Software that helps you comply with regulations. Fannie Mae, Wendy's and Walmart trust the best mobile inspection and audit platform. This will help you improve safety and accuracy. The #1 field management platform for teams, FORM OpX will transform your Excel, paper, and digital processes. FORM OpX combines advanced data gathering and configurable workflows with powerful operational insight to increase compliance in real time. To ensure compliance and team compliance, you can set up audits, inspections, or workflows. Digital forms allow you to capture data and guide teams to the right actions. Set up automated alerts and escalates to prompt corrective action when issues arise. You can save time and money by creating customizable workflows that improve processes, increase compliance, and reduce errors.

TestRail's web-based software test case management allows you to efficiently manage, track, report, and report on your software testing. Team productivity can be boosted with real-time insight into testing progress. TestRail's intuitive interface allows you to collaborate with others using comments, attachments, and feedback loops. Create personalized to-do lists. Get email notifications. Forecast test completion dates and estimate effort. Start testing and select cases to be executed using powerful filters. You can track progress using historical time data. To adjust assignments and resources, monitor the workload of your team. Capture the results from manual testing or receive real-time feedback via test automation. Create traceability and coverage reports that cover requirements, tests, and deficiencies. Generate meaningful reports Compare the results from multiple configurations and test runs. TestRail integrates seamlessly with the most popular issue tracking and test automation tools. Get the Atlassian Marketplace free TestRail JIRA plug in

QIMAone allows global brands, retailers, and manufacturers in the consumer goods industry to digitize quality and compliance operations, collaborate and collect reliable data across their entire supply chain, minimize disruption, improve visibility, and drive continuous improvement. Digitize your quality management, connect with your supply network, and collaborate with suppliers to avoid defects. Assign inspections to suppliers and inspectors, and then work together to correct the situation. Import, create custom workflows, checklists and checklists to support inspections and audits. To boost your supply chain, consolidate actionable KPIs and benchmark. Visualize your supply chain and use risk-based strategies for proactive improvement programs. You can reduce costs and spend more time on value-added activities by automating standard processes and automation. With actionable insights, elearning content, and collaborative tools, empower your factories and vendors.

ACE Essentials is the pre-validated Electronic Quality Management System Software (EQMS) designed for highly regulated industries. ACE Essentials includes 10 workflows, as well as all the required Standard Operating Procedures (SOPs) and Policies. This ensures that your quality management system is fully compliant from the start. ACE Essentials features include a complete audit trail that tracks every action within the system. This allows you to understand the risks associated assets. Features of ACE Essentials Pre-Configured Workflows Pre-Configured Event Management (Due dates, Scheduling, Reminders) - Pre-Configured Permission Based Security - Pre-Configured Full Documentation - 50+ documents - Multiple Site Capability - No Charge Upgrades for the Product's Life Pre-Configured Tasks Liste - No Validation Period Pre-Configured In System Notifications Pre-Configured Email Notifications

QwizPRO revolutionizes quality management for compliance with ISO 9001 and AS9100, making audits effortless and efficient. By utilizing its intuitive automation, the platform reduces errors, conserves time, and enhances the compliance journey. In the fiercely competitive landscape of modern business, QwizPRO is crucial for achieving quality excellence without complications. It enables consistent monitoring and assessment of suppliers, ensuring they meet your rigorous quality standards. Featuring real-time analytics and customizable reporting options, the software provides insightful visibility into supplier performance, showcasing strengths while pinpointing potential vulnerabilities. Equip your team with tailored QMS training that progresses from a basic grasp of industry standards to a comprehensive understanding of intricate procedures. QwizPRO facilitates automatic training deployment, tracks learning advancements, and uncovers areas needing improvement. Additionally, the software ensures immediate access to essential documents necessary for daily operations, further optimizing productivity and efficiency. With such capabilities, QwizPRO stands out as an indispensable tool for organizations striving for continuous quality enhancement.

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.

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.

Tailored solutions for your unique requirements are now within reach. Sustain your ISO 9001:2015 certification effortlessly with inblueQMS, while providing swift solutions to clients using inblueRequest. Capture customer needs and monitor your response times effectively, all while classifying various registers. Experience the convenience of managing everything online, backed by over three decades of expertise in information technology development. The advantages of our software include enhanced centralization for planning, recording, and tracking processes and procedures. You will receive timely reminders for deadlines and notifications whenever a task is assigned to you, delivered via email or through dashboards. The platform is adaptable, allowing you to adjust fields to suit your company's specific realities and to set permissions and deadlines. Enjoy an intuitive user interface designed to simplify your tasks, complete with guided functions. Additionally, you can document comments and versions for thorough tracking, as the system maintains a detailed history of changes. Furthermore, the software provides insightful charts and result reports to help you gauge performance effectively.

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.

Apollo Root Cause Analysis™ is a method grounded in principles that aids individuals in mastering effective strategies for problem-solving. When paired with the RC Pro® software, it enables the development of a comprehensive, evidence-based comprehension of any issue encountered. Such an understanding of the root causes and their effects fosters solutions that gain acceptance across the entire organization. The Apollo Root Cause Analysis™ approach promotes the establishment of a shared understanding through collaboration with all relevant stakeholders, resulting in a solid evidence-based perspective on the problem at hand. This methodology guarantees that the solutions implemented tackle verified causes, thereby minimizing the chances of future occurrences. It simplifies the problem-solving process and equips trained individuals with the necessary skills to tackle real-world challenges more efficiently and effectively. Additionally, RC Pro serves as a versatile root cause analysis software solution that can be customized for businesses of any scale and in various sectors. By utilizing RC Pro, organizations can enhance and integrate their problem-solving capabilities, leading to improved outcomes. Ultimately, this synergy between Apollo Root Cause Analysis™ and RC Pro empowers teams to create lasting solutions that foster continuous improvement.

Automate the identification and resolution of problems in your organization and supply chain. This is one of the most trusted CAPA software applications. It has been trusted by thousands of users worldwide. CAPA Manager corrective actions software automates the assignment of corrective actions, notification, investigation and reporting. It prevents errors in the control of the entire CAPA process from initiation through investigation and closure. CAPA Manager meets all requirements of the most important quality management standards, including ISO 9001, AS9100 and TS 16949. It maintains records of root-cause and corrective actions, and provides pre-defined workflows with approval gates.

Issues such as incomplete dynamic fields, excessive communication, and overlooked deadlines can emerge when a robust Quality Assurance (QA) process is lacking. With the evolution and frequent changes in privacy laws, it becomes essential to comply with international legislation regarding privacy standards. This is where Munvo’s CampaignQA© steps in, ensuring continuous adherence to necessary regulations. This innovative solution enhances your marketing automation system while streamlining overall marketing execution processes efficiently. It allows for the automation of validation in both inbound and outbound marketing campaigns, accompanied by comprehensive alerting and reporting capabilities to track performance. Additionally, users can easily manage contact frequency controls through a user-friendly drag-and-drop interface that requires no coding skills. Furthermore, it supports a rules-based approach to ensure the quality of marketing data and marketing datamarts. As a result, organizations can significantly improve their operational efficiency and maintain high standards of compliance.

iPassport is an advanced software solution tailored for healthcare laboratories, aimed at enhancing the digitization, organization, and overall management of quality and compliance on a daily basis. This platform offers a comprehensive array of quality management modules, making it simple to oversee various aspects, from document control to employee training. All controlled documents are conveniently centralized, complete with designated access and editing permissions, alongside thorough revision histories. It encompasses everything necessary to manage both internal and external audits effectively. Users can record and oversee non-conformities, corrective actions, and incidents, while also managing staff training, competencies, tasks, meetings, and leave. Additionally, it features a robust supplier database and auditing tool that includes performance evaluations. The system also allows for efficient management and tracking of assets and inventory, including comprehensive maintenance records for equipment. With iPassport, healthcare laboratories can ensure operational efficiency and compliance with regulatory standards.

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.

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.

SoftExpert EQM stands out as an all-encompassing enterprise quality management software (EQMS) that aids organizations in obtaining and upholding ISO 9001 certification by automating and enhancing quality processes specifically designed for their unique products, operations, and business practices. This modular and adaptable platform integrates all essential quality initiatives, including process mapping and the management of documented information such as standard operating procedures, work instructions, and records, along with non-conformance reports, corrective and preventive actions, and quality indicators. Furthermore, the software efficiently oversees supplier relationships, addresses customer complaints, conducts quality audits, manages training and competencies, and evaluates quality risks and controls, as well as quality inspections and statistical process control, all of which contribute to a more agile and resilient quality management system. By streamlining these diverse functions, SoftExpert EQM empowers organizations to enhance their overall quality performance and compliance.

Workflows are specifically developed to assist you in preparing all necessary components for a 510(k) submission, while also ensuring compliance with the quality record requirements set forth in 21 CFR Part 820 as you prepare to market your device. These workflows come equipped with tools to facilitate the drafting of essential policies, procedures, and work instructions. Furthermore, you can monitor non-conformances, deviations, and CAPAs through tailored quality management reports. As your processes evolve and enhance, you can ensure your team receives automatic training updates. The system also automates validation testing for devices, applications, websites, and custom software tailored to your business needs. This automation significantly reduces the time and resources that would otherwise be consumed by extensive testing, reporting, and approval processes. Additionally, you can compile all your policies, procedures, and artifacts into standard documents, making them readily available for audit evaluations. Overall, this solution streamlines the compliance and validation processes, thereby enhancing operational efficiency.

In the realm of food manufacturing, it is essential for buyers, production, technical, and quality personnel to collaborate effectively as a cohesive TEAM in order to generate food products that are not only profitable but also safe and of superior quality. 3iVerify presents an economical and secure cloud-based food safety management system designed to assist technical, quality, and compliance managers in navigating the overwhelming array of processes, procedures, and documentation they encounter daily. Our straightforward and logical approach addresses crucial processes such as managing supplier and material approvals, monitoring suppliers, handling document management, and overseeing corrective actions. We believe that spreadsheets and excessive paperwork should not consume valuable time, as we strive for efficiency. By working closely with our clients, we ensure that our system is customized specifically to fit their unique business needs and operational structure. We offer flexibility by providing only the necessary modules, preventing unnecessary expenses for features that clients may not utilize. For a detailed overview of our solution and its advantages, please explore our website for more insights.

Enhance the quality of incoming parts and supplier performance to mitigate the risk of production halts while optimizing the overall cost of ownership and managing supply chain uncertainties. Continuously monitor in-process quality and track trends throughout the production cycle, implementing proactive measures to decrease the failure rate. Oversee and ensure the quality of products ready for shipment, thereby boosting their competitive edge in the market. Prioritize customer needs by swiftly addressing complaints and enhancing service and quality, ultimately leading to increased customer satisfaction. Document and track corrective and preventive actions effectively, while providing real-time updates on each team member's task progress. Strengthen the culture of continuous improvement and refine the corporate quality management system. Streamline the audit preparation process to enhance both efficiency and effectiveness, ensuring compliance with required regulations through a reliable mechanism that supports scheduled audits. This comprehensive approach not only promotes a high standard of quality but also fosters a proactive environment committed to excellence.

ApTest Manager is a versatile, web-based tool designed to enhance the efficiency, productivity, and availability of information in testing processes. Users can input requirements and tests directly into the platform online, making the data instantly accessible to the entire team for documenting test requirements, specifications, and plans. This allows for the execution of thorough, repeatable test cycles while facilitating the review and comparison of test results. Additionally, it supports the automatic import of existing requirements and tests, streamlining the process further. ApTest Manager takes charge of managing the execution of test cycles, providing testers with the relevant requirements, procedures, and environments they need for each test. Once a test has been executed, results are promptly recorded in the system. This ensures that consistent procedures and outcomes are maintained across different test runs, regardless of whether the same team members are involved. Overall, ApTest Manager significantly contributes to improving the overall quality and reliability of software testing.

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.

EASE is an innovative platform that allows manufacturers to conduct safety audits, layered process audits, and 5S. EASE provides visibility and accountability to the plant floors through real-time data. It streamlines how manufacturers conduct, respond and administer plant floor audits. Forget about pencils and paper. The EASE mobile app guides you through audits, including responses to non-conformances. Annotated photos provide visual evidence. Issue tracking allows you to assign issues to the right people and ensure that they are closed out. Interactive dashboards and customizable reporting provide real-time audit results by line, plant or region, and insight into the business unit.

myQualityTM serves as an online portal for ISO 9001 quality management systems tailored for both quality professionals and consultants. It offers a thorough collection of necessary documented information that is ready for assessment, design, implementation, certification, and continuous support. Gaining a basic understanding of the platform is straightforward, but fully leveraging its robust capabilities will require additional time and will be integral to your ongoing improvement efforts. Merely purchasing the software and completing the training is akin to acquiring a computer solely for web browsing; true value emerges when you learn to optimize it as a genuine investment. Fortunately, we offer an extensive range of 'How To' resources alongside our Tech Support to assist with all other inquiries. The platform is equipped with the essential documented information requirements through user-friendly, interconnected databases, registers, templates, forms, procedures, and a plethora of other resources. A one-time setup fee grants you a dedicated company domain, five managerial accounts, and unlimited user access, ensuring your team can fully engage with the system. This setup not only streamlines your quality management processes but also positions your organization for sustained growth and compliance in the future.

SoftTech Health provides an extensive array of quality management software solutions specifically designed for the healthcare sector today. By offering seamless integration, you can efficiently consolidate all your quality management activities into one user-friendly software platform. Our Accreditation Manager is designed to assist you in preparing for upcoming inspections, equipped with features that allow you to easily compare and transfer data from prior inspections. It automatically monitors compliance evidence, ensuring that crucial details are not overlooked. Each inspection requires careful attention to detail to guarantee that all requirements are met; it also aims to minimize the time spent on coordination, tracking, and reporting during audits, while simplifying the often tedious process of collecting supporting documentation. The Accreditation Manager not only streamlines these essential tasks but also enhances compliance and positively impacts your financial outcomes, demonstrating its value across multiple facets of healthcare management. Additionally, this software empowers organizations by providing insights that can lead to continuous improvement in quality management practices.

Solutions that prioritize safety, compliance, and employee training in the workplace are essential. For over twenty years, SMG has established itself as a reliable ally in process management, enhancing workplace safety, and ensuring compliance with OSHA and various regulatory standards across local, state, and federal jurisdictions for diverse businesses, including food service distribution centers, restaurants, and LTL freight carriers. Leveraging software-based expertise in health and safety management, SMG enables your organization to maintain compliance effortlessly, minimize costly incidents, and streamline operations and logistics. Transition away from generic policy documents and neglected safety plans by utilizing proactive software tools that integrate smoothly with your processes for training staff, performing safety audits, documenting incidents, and implementing corrective measures. By adopting these innovative solutions, businesses can foster a culture of safety and efficiency that benefits both employees and the organization as a whole.

Honeywell's TrackWise Digital® serves as an innovative cloud-based Quality Management System (QMS) aimed at enhancing the efficiency of quality and compliance processes within organizations. Drawing on nearly thirty years of expertise in the field, it features integrated modules that cater to various elements of quality management, such as document control, training oversight, and corrective and preventive actions (CAPA). The platform utilizes cutting-edge digital technologies, including artificial intelligence and machine learning, to deliver actionable insights in real-time, which fosters a proactive approach to quality management. Its adaptable, modular framework ensures smooth integration with current enterprise systems, allowing for quick deployment and growth. By optimizing quality processes and maintaining adherence to industry regulations, TrackWise Digital® enables organizations to accelerate product launches while effectively reducing risks. This comprehensive system not only enhances operational efficiency but also supports continuous improvement initiatives across the quality management spectrum.

Starting now, you can effortlessly obtain all the essential documents without sacrificing your valuable work hours and at an attractive price! The subscription process is straightforward; just a few clicks will bring you to the purchase screen. There, you can input your company’s details, including the organization name, logo, and information regarding the procedures approver. Simply complete the forms and implement them according to the ISO 9001 standards presented on your screen. You can easily access controlled reports and forms featuring your organization's name and logo, ensuring you’re well-prepared for the external audit. You can also handle the preparation on your own time, eliminating the need for external assistance. The system is available all year round, allowing you to enter data whenever it suits you. Don’t leave things to the last minute! Everything you need for a robust quality management system is included, along with the ability to create controlled forms emblazoned with your company logo. This all-in-one solution ensures you have everything necessary for the external audit and your ISO quality management system conveniently at your fingertips. By streamlining the process, you can focus on what truly matters—growing your business.

Accelerate your innovation and ongoing improvement efforts by three times within just 30 days with Unifize, a comprehensive software platform designed to foster collaboration in innovation, quality, and continuous improvement processes. This solution enables manufacturing companies to create superior products more efficiently. You can initiate with a single application or implement Unifize across all departments, ensuring seamless integration into your operational framework. The platform features highly customizable templates that dismantle silos by interlinking your processes effectively. Unifize stands out as the only PLM tool dedicated to uniting teams in a dynamic, real-time collaborative setting, allowing for efficient problem-solving and management of essential innovation workflows. For those seeking to enhance their quality management capabilities, Unifize is the ultimate eQMS that transforms every quality procedure into a collaborative and straightforward endeavor. It’s time to stop merely acknowledging your APQP/PPAP processes; instead, cultivate teamwork through dedicated real-time discussions for each record, ensuring that every aspect of quality management is actively engaged. This proactive approach not only improves accountability but also drives a culture of continuous improvement throughout the organization.

AirManual makes it easy to combine a checklist and guidance that explains what each step is. Ideal for training and recurring processes. AirManual allows teams to document their processes, training, and onboarding. AirManual combines a user-friendly tool with free consulting. We'll help you prioritize and address your most pressing issues. Our customers enjoy a better quality of life, faster growth, and longer vacations as a result. A home for documentation, processes, and training. Your team will find the documentation they need and be able to solve their own problems. AirManual is a tool that works for all teams. AirManual works for every team. Start in the most important area and then scale it up as you need it. Stale documentation is gone. It's easy for your team to review usage and get feedback. AirManual users who are new to the platform can receive free consulting. We will help you move faster and avoid common pitfalls.

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.

EHS Software Tailored to Your Specific Workflow. Modify Capptions to align with your established health and safety protocols rather than conforming to a rigid system. Capptions provides a flexible framework that empowers you to design a personalized EHS management platform, even without a specialized development team. This versatile cross-platform application ensures that your EHS management system seamlessly integrates with your workflow. Capture EHS data anywhere, anytime, whether you are online or offline, using any device. Create unlimited custom data capture applications without the need for coding expertise. Safeguard your EHS data with robust security measures like SSL256 encryption and blockchain technology. Effortlessly connect your EHS platform with existing IT systems and enjoy a plethora of additional features. Companies of all sizes worldwide have placed their trust in us, as traditional EHS management software often necessitates adjusting your processes, but Capptions allows you to retain your methods. By choosing Capptions, you can enhance your operational efficiency while maintaining compliance with health and safety regulations.

WinSPC real-time statistical process control helps manufacturers create the highest quality product for the lowest possible cost, achieving regulatory compliance, and optimizing yield while reducing scrap, waste, and rework. WinSPC collects shop-floor data in real-time from virtually any source. Dashboards with charts and real-time statistics summarize current production performance within a single screen while triggered actions connect WinSPC to remote systems and stakeholders. Key WinSPC functions: Monitor - Empower everyone with actionable intelligence. WinSPC displays real-time control charts on the shop floor, enabling your team to immediately detect and correct process issues. Alert - Close the quality loop from "detection-to-correction" with actions to visually alert or take action for you when violations occur. Analyze - Experiment, visualize and reveal more about any variable using the one-click variable analyzer. Mine your data to detect relationships and reveal new insights for improvement. Report - Quickly create, publish, and share quality reports across your organization using our graphical report builder and dozens of starting templates.

A software solution designed for conducting and automating the scoring of assessments is available through the ERS Data System, which equips users with essential information and tools to ensure precise evaluation outcomes. This system is versatile enough to support both technical assistance and high-stakes assessments, effectively saving time while enhancing the overall quality of the assessment procedure. Additionally, the ERS Data System features up-to-date clarifications directly from the authors, along with supplementary resources like USDA meal guidelines, playground safety regulations, and best practice advice on topics such as handwashing, sanitizing, and diapering procedures. Moreover, assessors can document their insights using worksheets that gather critical information for scoring each element accurately. Notes made by assessors during the evaluation are transformed into text for reporting purposes, ensuring clarity and accountability. Comprehensive reports can be generated for various levels, including classroom, facility, and organization, allowing for detailed analysis and informed decision-making. This multifaceted approach not only streamlines the assessment process but also fosters a deeper understanding of best practices in educational settings.

You, as a business, must comply with all laws and regulations in the jurisdictions where you operate. Failure to comply with Regulatory Compliance requirements could result in severe penalties or fines, as well as reputational damage. Need help with protecting your digital data from unauthorized access or data loss prevention? How to comply with GDPR? All questions can be addressed by our Data Governance and Data Security experts. Are you frustrated by manual, time-consuming processes and procedures in your workplace? We can help you automate your Health and Safety checklists and Risk Assessments, CAPA, and other compliance requirements. Finding cyber risk management confusing? From training staff awareness to consultancy services, we have everything you need to help your organization with cyber security. The list below shows the top regulatory compliance issues that businesses will face in the next year.

We have created user-friendly and effective tools to streamline your EDM and the validation process for your documents. Accurately monitor your workflow through intuitive dashboards, customized forms, and real-time metrics. With Qualios, manage your workflow efficiently using two seamlessly integrated tools that enhance the management of your information system. Ensuring that your information is current and easily trackable is crucial; our Qualios Doc solution empowers you to oversee your documents and track their progress. Qualios Manager is flexible enough to accommodate your specific quality indicators! Generate straightforward and informative forms and dashboards to swiftly oversee your internal workflow. The improvement process necessitates prompt oversight of all your operations. Qualios is designed to support your quality commitment and assist you in adhering to ISO 9001, ISO 14001, or 18001 standards. Additionally, these enhancement processes should be straightforward and not overly burdensome. By implementing our solutions, you can focus more on your goals and less on administrative tasks.

Enhance the efficiency of your plant floor through high-definition visibility, foolproof management, and a real-time production environment that seamlessly integrates with your ERP by design. Traditional ERP systems were not specifically built for manufacturing execution, and relying on post-production information, or “back-flushing,” does little to aid in controlling output during the manufacturing process. Plex’s Manufacturing Execution Suite (Plex MES) offers real-time production oversight, providing immediate access to manufacturing data for comprehensive visibility and effective closed-loop control. This adaptable, cloud-native solution is crafted for straightforward deployment, standardization, and seamless integration with your existing corporate ERP. The suite comprises a collection of unified shop floor applications operating on a shared database, minimizing the potential for disruptions or errors caused by inter-application connections. With a focus on a paperless environment, it is user-friendly, empowering operators to boost productivity while eliminating manual process errors, ultimately transforming the way manufacturing operations are conducted. By integrating these systems, businesses can achieve a more streamlined and efficient manufacturing process.

A collaborative platform that simplifies and digitizes the management of suppliers and purchasing. You can manage your supplier and quality management processes on one platform with the supplier and quality modules. The negotiation and contract management modules can help you optimize your negotiations and cut down on hiring times. It digitizes the formalization of orders with the various order management and billing modules.

The Plex Quality Management System (QMS) enables both process and discrete manufacturers to adhere to stringent industry standards and customer requirements through an integrated digital record-keeping system. By facilitating consistent and reliable quality assurance via in-line quality measures, transparent reporting, and straightforward audit tracking, it ensures that manufacturers can maintain compliance effortlessly. With real-time access to quality documentation available digitally throughout the organization, businesses can effectively meet regulatory demands while fostering operational efficiency. Enhanced delivery performance, improved supplier relationships, and greater customer satisfaction contribute to sustained growth in both new and repeat business. By embedding quality management into everyday workflows and processes, the risk of quality-related losses, warranty claims, or product recalls is significantly minimized, ultimately enhancing brand image and customer loyalty. Furthermore, Plex enables the creation of detailed process control plans that include specific inspection protocols and digital checklists, streamlining quality oversight across various operational areas. This comprehensive approach to quality management not only safeguards compliance but also drives continuous improvement and innovation within the manufacturing sector.

Transform your Life Sciences operations by significantly enhancing the control, efficiency, and quality of your products and processes. Maintain inspection readiness consistently with our fully compliant platform, which has undergone pre-validation in line with GAMP5 standards. Gain complete oversight of your processes and documentation, allowing for perfectly customized workflows and maximized automation wherever feasible. Experience smooth operations and comprehensive traceability through our seamlessly connected modules. Our committed team is available to address any inquiries you may have at any moment. Only the finest Scilife experience meets our high standards! The Scilife platform not only streamlines but also automates and organizes every aspect of your industry, whether in Medical Devices, Pharma & Biotech, or ATMP. Click below to explore the specific Scilife modules that cater to the distinct lifecycle stages within your industry. Our software is not just equipped with all the essential quality tools you would anticipate; it also comes with numerous additional features that surpass expectations, ensuring your operations thrive. We're excited to partner with you on this transformative journey!