Alternatives to inblue QMS

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.

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.

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

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

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.

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

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.

Transform your paper-intensive management system into a paperless environment. The Documentation module allows you to manage the review, modification and approval of your documentation. You can record and manage any problems caused by defects in products, services, or systems within your organization. You can organize your data according to the regions, products, types, processes, and risks you have identified. In the software, create a schedule for internal audits and supplier audits. Assign responsibilities and link audit findings to planned audits. You can schedule maintenance and calibration tasks on a regular basis, according to the frequency you specify. The software retains task records and attachments. This module is offered as a complement.

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.

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.

QwizPRO simplifies ISO 9001 and AS9100 quality management, ensuring stress free audits. Its user-friendly automated minimizes errors and saves time. QwizPRO allows for quality excellence in today's competitive environment. Monitor and evaluate every supplier consistently to ensure they are aligned with your stringent standards. The software's real-time analytics, customizable reporting, and other features provide a clear picture of supplier performance. It highlights areas of excellence, and identifies potential risks. Your team will benefit from QMS training designed to help them progress from understanding industry standards quickly to mastering complex procedures. QwizPRO lets you automatically deploy training, track learning progress and identify areas that need further development. Use QwizPRO to get instant access to the documents you need for your daily tasks.

Apollo Root Cause Analysis™ is a principle-based method for solving problems that will help you master problem-solving techniques. Using RC Pro®, you can quickly and easily create an evidence-based understanding for any problem. Effective solutions can be found within your organization when you have a solid understanding of the causes and effects. Apollo Root Cause AnalysisTM facilitates the creation and acceptance of a common reality by involving all stakeholders to create an evidence-based understanding. This ensures that your solutions address proven causes and prevent future problems. It makes problem solving easy and gives those who have been trained the skills to solve real-world issues more efficiently and effectively. RC Pro is a flexible and comprehensive root cause analysis software solution that is suitable for companies of all sizes and in any industry. RC Pro allows you to integrate your problem-solving capabilities.

Solutions tailored to your needs. InblueQMS helps you maintain your ISO 9001 certification. With inblueRequest, you can provide fast solutions to your customers. Register your customers requirements, measures your response times. Classify Registers Do everything online. With more than 30 years of experience in the development and maintenance of information technology. Our Software offers many benefits. Centralization Planning, recording, and follow-up on processes and procedures. Reminders. Notifications and reminders sent via email and dashboards when a task is assigned. You can manage it. Modify fields to reflect the needs of your company. Give permissions and set deadlines. It is simple to use. Easy to use, with guided functions that make it easy. Recording. For a better follow up, record comments and versions. Includes a history and description of all changes. Charts and results-reports.

Without a proper Quality Assurance (QA), issues such as missed deadlines, incomplete dynamic fields, and overcommunication can all arise. It is becoming more important to ensure that privacy legislation is adhered to internationally as privacy laws evolve and sometimes transform. Munvo's CampaignQA(c), ensures compliance with all regulations. This technology can be used to complement your marketing automation system, and to improve overall marketing execution in a timely manner. Automate the validation of outbound and inbound marketing campaigns, and monitor the results using robust alerting features and reporting. Easy-to-use drag-and-drop interface allows you to manage contact frequency controls (no programming required). Allow rules-based validation for marketing data/marketing datamart quality.

Walsh QA Inspector makes it easy to track and manage all aspects of your QA program. Access all your checklists, including people, locations, items, standards, and procedures, from your smartphone or tablet. If data doesn't tell the story, it is useless. You can choose from dozens of storylines that provide unique insights and conclusions. Score reports, performance reports, frequency of deficiencies, work not completed, ATP scores, and many more. Filter by date and location, housekeeper, inspectors, supervisors, checklist. We can import names and emails from within your facility, including supervisors, inspectors, informed parties, administrators, and other responsible parties. With their smartphones or tablets, anyone can conduct inspections, rounds, and surveys. Send follow-up emails automatically and escalate as necessary. Later, people will be reminded about pending tasks and due dates.

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.

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.

SoftExpert EQM (enterprise quality management software) is the most comprehensive. It assists companies in achieving and maintaining ISO 9001 certification by automating highly interactive quality processes that are tailored to their specific products, operations, and business practices. As a modular and scalable solution platform, SoftExpert Quality Management Software seamlessly integrates all key quality initiatives, including process mapping, documented information (SOP - standard operating procedures, work instructions and records), non-conformance reports (NCR/NCMR), corrective/preventive actions (CAPA), quality indicators (KPIs). The solution can also manage supplier relations, customer complaints and quality audits, as well as competence and training, quality controls, quality inspection, and statistical process control, increasing QMS flexibility and robustness.

iPassport, a managed software service for healthcare labs, is designed to digitize, streamline, and improve the day-to-day management of quality and compliance. iPassport offers a complete suite quality management modules that allow you to keep track of everything, from document control to staff training. All your controlled documents are stored in one location with the appropriate access and edit rights and complete revision history. All the information you need to keep track of external and internal audits. Record and manage CAPAs, incidents and NCs. Manage staff training, competencies, tasks, and leave. A complete supplier database and an audit tool, including performance reviews. Manage and track stock and assets, including maintenance records.

To produce high-quality, profitable food products, the food manufacturing business needs buyers, technical, quality, and production staff to work together. 3iVerify, a cloud-based, affordable food safety management system, helps technical, quality, and compliance managers manage the tidal wave process, procedures, and paperwork they deal with every day. This is achieved by using a simple and logical approach to key processes such as supplier and material approvals management, supplier monitoring and document management and corrective actions management. We believe life is too short to be surrounded by spreadsheets and paperwork. We work closely with our customers to ensure that their system is tailored to their business model. We can only offer you the modules that you need so you don't have to spend money on things you won't use. Visit our website to learn more about the solutions we offer.

Virje complies to 21 CFR Part 11, 21 CFR Section 820, ISO 13485. Are you overwhelmed by the idea of Part 11 software validation Accessible wherever you are, whenever you work. Automated collaboration and automation can help you reduce paper, lower costs, and increase efficiency. This is the ideal solution for small- to medium-sized businesses. This system was designed specifically for quality control of medical devices. The system is flexible enough that it can adapt to your workflows without having to compromise. Modifiable change order approvals can be configured by employee role or by document type. Notifications to the responsible personnel at each stage of the change process. Ability to identify material dispositions for individual documents. Access to historical and released versions of documents is easy. Quick access to document history. Tracking of locations and distribution of hard copies. Notification of periodic document review.

ApTest Manager is a Web-based, general purpose tool that can be configured to increase the speed, productivity, and accessibility to information in your testing processes. ApTest Manager allows you to enter requirements and tests online. Your entire team can instantly access the information to create test requirements, test specifications and test plans, execute repeatable comprehensive tests cycles, and review and compare test results. You can import existing requirements and tests automatically. ApTest Manager manages the execution of test cycles. Each test environment is described to the tester. After the test has been completed, the test results are entered into ApTest Manager. This ensures consistency and consistent results, regardless of whether different personnel are performing the testing.

These workflows will help you create everything you need for a 510(k), and create quality records for 21 CFR Part 820 when you are ready to sell your device. Built-in tools for creating policies, procedures, or work instructions. With customized quality management reports, you can track non-conformances, deviations and CAPAs. Keep your team trained as you improve and scale your policies, workflows, and procedures. Automate validation testing for devices, apps, web and custom-made software. Reduce the time and resources required for lengthy testing, reporting, approvals, and other tasks. All your policies, procedures, artifacts can be converted into traditional documents for audit review.

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.

Optimize the quality of incoming parts and supplier quality performance, reduce the risk of production disruption, optimize the total cost-of-ownership, and manage supply chain risks. Monitor the quality of in-process production and the trends throughout the production process. Take preventative actions to reduce the failure rate. Improve product competitiveness by monitoring and controlling the quality of products to be shipped. Customer focus. Rapid response to customer complaints, Improve service and quality, increase customer satisfaction. Follow up on corrective and preventive actions. Real-time monitoring of each member's progress. Enhance the ability to continuous improvement and improve the corporate quality management system. Reduce time spent on audit preparation. Increase efficiency and effectiveness of audits. Mechanism in place to facilitate the compliance of the requirements and regulations with the audit.

SoftTech Health has the best quality management software tools in healthcare today. Because they integrate seamlessly, you can streamline all of your quality management tasks with one simple-to-use software package. Our Accreditation Manager will help you manage any upcoming inspections. It includes tools that allow you to compare and copy work from previous inspections. You can automatically track evidence of compliance and make sure nothing slips through the cracks. You want to make sure that all requirements are met. Reduce time and effort in coordinating, tracking, and reporting on audits. Streamline the tedious process of gathering supporting evidence. Accreditation Manager automates these processes, increasing compliance and the bottom line.

Online document management makes it easy to create and manage documents. This prevents lost printed copies and a lack of organization. All information can be gathered in one place, making it easy to track and address any nonconformities. To aid you in decision making, define, collect and analyze KPIs using comparative charts. You can plan and execute actions to address opportunities and risks in a controlled and simple way. Get rid of spreadsheets and printed copies. Access file control in a cloud database with 24/7 access from any device and location. Optimize document review, approval, and elaboration. Manage access permissions, and receive automatic notifications about document changes or expiration dates. Genebra always has the most current version of any file that is uploaded. Don't waste time looking through multiple spreadsheets and don't lose any revisions.

Honeywell TrackWise Digital® is a cloud-based Quality Management System (QMS) designed to streamline and enhance quality and compliance processes for businesses. With decades of expertise behind it, the platform offers robust modules for managing critical functions like document control, training programs, and corrective and preventive actions (CAPA). Utilizing advanced technologies such as artificial intelligence and machine learning, TrackWise Digital® delivers real-time insights to help organizations identify and address quality issues proactively. Its modular, flexible design ensures smooth integration with existing enterprise systems, enabling quick deployment and easy scalability. By optimizing quality operations and ensuring regulatory compliance, TrackWise Digital® supports organizations in accelerating product delivery while reducing operational risks.

myQualityTM is an online portal for ISO 9001 quality management system consultants and quality practitioners. This comprehensive collection of information is available for assessment, design, implementation and certification. It is easy to learn the basics. It will take some time to learn how to harness the software's full potential. This can be part of your ongoing improvement strategy. It is not like buying software and then getting training. It is important to learn how to make the software a worthwhile investment. We offer a complete suite of 'How Tos' along with Tech Support for everything else. The platform provides the minimum documentation requirements through intuitive, interconnected databases and registers, as well as templates, forms, procedures, and forms. One-time setup fees include a company domain, unlimited users, and x5 managers.

In just 30 days, you can triple your innovation speed and improve your continuous improvement. Unifize is a software platform that facilitates collaboration in innovation, quality, CI, and other areas. This allows manufacturing companies to bring better products to market faster. Unifize works in any environment, no matter if you use it for one function or all. Templates are customizable to your needs and allow you to connect all of your processes. Unifize is the only PLM platform that focuses on bringing together teams in a real-time collaborative environment. This allows them to solve problems and manage important innovation processes. Look no further if you are looking to upgrade to a complete Quality Suite. Unifize is an eQMS that makes quality processes collaborative and simple to follow. Don't just pay lip service to your APQP/PPAP process. Teams can come together for a dedicated conversation in real-time about each record.

Software & Services that ensure your workplace is safe, compliant, as well as properly training your employees. SMG has been a trusted partner in process management, improving workplace safety, as well as ensuring OSHA compliance at the local, state, federal levels. This applies to businesses that range from restaurants and food service distribution centers to LTL freight carriers. SMG's software-driven expertise on health and safety management enables your business to easily ensure compliance and reduce costly incidents while improving operations and logistics. You can replace outdated safety plans and policy documents with action-driven software tools that seamlessly integrate into processes for training employees, conducting safety audits and reporting incidents.

ShopXpert, a fully integrated manufacturing software, is designed to support the entire manufacturing process, minimizing data entry, and increasing productivity. It automates manual procedures to reduce inefficiencies and slow down job shop performance. The software has a variety of modules including standard modules, supplier and outsource management, jobs for employees, vending, costing tools, forms, tasks, workstations, training notes, academy time clocks, in-app messages, storage, QR codes, and more. These modules offer functionalities such as dashboard access, customer management, document storage and customization, task scheduling, employee tracking and real-time communication. Employees can manage their jobs efficiently from their mobile devices or tablets, reducing the need for a desktop computer.

You can now get all the documents you need quickly and easily, without wasting valuable time and at a very attractive price. Subscription is easy. Just a few clicks and you will be taken to the order subscription screen. Enter your company data, logo, and information about approval. Fill out the forms and implement according to the ISO 9001 requirements. Get control reports and forms with your organization's name and logo. Prepared for external audit. Self-preparation in your own time without the intervention of an external party. The system is available all year round and data can be entered at any time. Don't rush! All the necessary information for a quality management program, including control forms with your company logo. Everything you need to complete the external audit and your ISO quality management program in one place.

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.

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.

High-resolution visibility, error-proofed controls, and a real time production ecosystem connected to your ERP-by-design will help you increase plant floor efficiency. ERP systems were not designed for manufacturing execution. Plant floor information available post-production--or "back-flushed"--doesn't help you control output at the manufacturing moment. Plex's Manufacturing Execution Suite, Plex MES, gives you real-time production control so you can have up-to the-second manufacturing data for end-to–end visibility and closed loop control. Flexible, configurable and cloud-native solution that can be deployed, standardized, and integrated with your corporate ERP system. A suite of unified shop floor applications that are all based on a common database. This eliminates the possibility of errors or disruptions caused by inter-application integrations. Operator control that is paperless and easy to use to increase productivity and eliminate errors in manual processes.

EHS Software that Fits Your Unique Workflow. Capptions can be adjusted to fit your existing safety and health procedures (not the other way around). Capptions are a set of blocks that allow you to create your custom EHS management platform, even if you don’t have a dedicated development staff. This cross-platform app allows you to: - Create an EHS management system custom to your workflow - Capture EHS data online and offline on any device - Create unlimited, custom data capture apps (without coding). Securely share EHS data with SSL256 and Blockchain - In no time, integrate your EHS platform into all other IT systems - And many more... Companies large and small around the world trust us. Most EHS management software on the market requires that you adjust your process. Capptions doesn't.

Software to automatically score and conduct assessments. The ERS Data System gives you the information and tools to accurately score assessments and conduct them. The ERS Data System is a time-saving and quality-enhancing tool that can be used to provide technical assistance or conduct high-stakes assessments. The ERS Data System integrates with the most recent notes from the authors for clarification, supplemental materials like USDA meal guidelines, playground safety standard, and best practices information (handwashing/sanitizing, diapering). Handwritten notes taken by the assessor are recorded in worksheets. This allows for the collection of information necessary to correctly score each item. The justification notes at the indicator level are handwritten during assessment and then converted into text for reporting. Reports can be created at three levels: facility, classroom, and organization.

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 simple and effective tools that will help you manage your EDM as well as the validation of your documents. Clear dashboards, customized forms, and real-time indicators allow you to track your workflow precisely. Qualios combines two powerful tools to help you manage your workflow. Qualios Doc allows you to manage your documents and their evolution, ensuring that up-to-date information is always available. Qualios Manager can be customized to suit your quality indicators. To manage your internal workflow, create clear and concise forms and dashboards. You need to be able to quickly control all your flows in order to improve your process. Qualios was designed to support your quality commitment and allow you to comply with ISO 9001 or ISO 14001 standards. These improvements should not be tedious or time-consuming

Plex Quality Management System helps discrete and process manufacturers comply with strict industry and customer requirements. It is a closed-loop digital record system. Ensure predictable, repeatable quality delivery Clear reporting and in-line quality are key to ensuring high quality. With digital quality documentation, the enterprise can meet industry standards and comply with customer regulations. Increase repeat and new business growth through on-time delivery, better supplier management, and customer satisfaction. Quality management is an integral part of your workflows and processes. This reduces quality loss and the risk of recalls or warranty issues. It also improves your brand reputation and customer relations. Plex makes it easy to share quality requirements and documentation in real time across the enterprise. Plex allows you to create process control plans that include detailed inspection instructions and digital checklists.

Revolutionize your Life Sciences processes. You can dramatically improve the quality, control, and efficiency of your products and processes. Our fully compliant platform is pre-validated according GAMP5. This ensures inspection readiness at all time. You have complete control over all documents and processes. You can also customize workflows and automate when possible. You can enjoy uninterrupted workflows and full traceability with seamlessly connected and integrated modules. Our dedicated team is available to answer any questions you may have. Only the best Scilife experience is possible! Our Scilife platform automates, automates and organizes all processes in your industry space, no matter if you're in Medical Devices or Pharma & Biotech or ATMP. Click below to see which Scilife modules are available for your industry's unique lifecycle stages.

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.

GlobalVision is the industry's leading review software. You can instantly detect and fix critical errors, so you can get to market faster and without compromising quality. Verify content as it passes through your workflow to improve speed and accuracy. You can quickly spot any errors by comparing files and identifying the differences. To speed up approval, reduce review time and avoid unnecessary delays between departments. For regulatory filings and internal reviews, ensure that copies are accurate. As your content develops, make sure that no bugs are created.

Ideagen Quality Control automates the quality inspections and documentation process for aerospace and defence, automotive, and medical device manufacturing companies. Implement a system to ensure your engineering and quality teams work together in harmony. This will guarantee traceable, compliant product development. Save time and resources by pulling elements directly from your testing source systems and publishing data into pre-built AS9102 PPAP and FAI report templates.

It is possible to get a complete overview of the document management system by separating all versions of a document into different modules based on their state (draft approved, valid, historic, and valid). Visual Quality registration forms are easy to create (using the built in HTML editor), and registration fields and workflows are more feature-rich than what our competitors offer. Visual Quality Web Access handles all registrations (requests, approvals, and rejections). Visual Quality is rapidly evolving thanks to the incredible Visual Quality community that helps shape the product. We are committed to providing you with the best software to build and maintain your quality management system.

Stability studies are complex and can be difficult to manage. The risk of making mistakes is higher when you use a paper-based system. A software-based solution that automates stability studies and shelf life analysis is the only way to go. Regulators are very strict about stability studies. Companies must be able prove the validity and reliability of their data. Automated solutions allow companies to produce the required documentation in real time to satisfy auditors. Nova-Stability systems help companies comply with regulatory requirements while reducing patient risk. Nova-Stability, a powerful process-based system with many features, manages all aspects of the stability testing process. This comprehensive solution conforms to all current regulations at a global level. Nova-Stability can accommodate all types of stability studies.

Are you a risk or quality manager in search of a powerful solution to your problems? ISO2HANDLE gives you superpowers to control your quality, safety and HR processes. ISO2HANDLE can be used by businesses in any industry. Our software provides capabilities such as risk and resource management, complaint management (including task management), risk assessment, registrations and notifications, document management (including audits), onboarding, evaluations of employees, expense claims, leave requests, and environmental measures. You can generate reports with just one click. This makes audits easy. We are proud to support hundreds of companies around the world from our base in the Netherlands.

VQMS is more than just a document management system. VQMS offers a Baker's Dozen of departmental options to your company. Check out the VQMS offerings. A Baker's Dozen. Vintara QMS provides comprehensive training on the application and the ISO process at your door. We provide a thorough exploration of ISO 9000 and ISO 13485, specifically designed to give your quality staff extensive insight into the process in a short time. Vintara offers a variety of training programs, from training for internal auditors to application-specific training on-site or online. We have a program that will meet your company's needs. Vintara understands that building, maintaining, and maximising your Quality Management System (QMS) can often require more than technology and training. We offer complete solutions, starting from the beginning.

The eInfotree™, Quality Management System, provides a unified approach for Enterprise Information Management. It links data and business processes in a highly intuitive way. This connectivity creates a highly productive and easy workspace that facilitates organizational synergy, operational efficiency, and profitability. We offer solutions from the plant floor up to the top floor, with an integrated enterprise data and document management solution. This creates an agile business environment. eInfotree allows your organization to capture, process, and manage information more efficiently. This improves customer service, reduces costs, and provides a great return on investment. A number of modules add value to the browser-based application.