Alternatives to SBS Quality Database

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

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

isoTracker Quality Management is a popular cloud-based quality management software (QMS) system. It is used on a worldwide basis by businesses to manage their ISO 9001, ISO 13485, ISO 22000, ISO 17025, ISO 14001 systems...plus many others. It is a modular product which can be configured to meet an organization's specific requirements and is competatively priced with superg customer support. Any module combination of Document Control, Complaints, CAPA, Audits, Training, Non-Conformance and Risk can be subscribed to.

Dot Compliance offers the industry's first ready to use Quality Management Solution powered by the Salesforce.com platform. The Dot Compliance solution includes an extensive set of off-the-shelf ready eQMS and compliance pre-configured processes, enabling customers to deploy quickly and cost effectively. Dot Compliance ready to use solutions include full project validation services and product validation packages. Dot Compliance offers the industry’s most cost-effective quality and compliance management solution available, allowing users to quickly deploy flexible and scalable solutions. Automate core quality processes such as Document Management, Training Management, CAPA, Audits, Customer Complaints, Change Management, Supplier Quality, and more. Our solution is fully configurable and offers seamless integration abilities, with easy adaptation and implementation of customer’s specific requirements.

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

The SBS QMS Suite consists of 5 software modules that work together for efficient Quality compliance: SBS Quality Database - CAPA / 8D corrective and preventive actions (CAR) with root cause analysis - Nonconformance management - Risk analysis including FMEA, SWOT, interested party risk register - Internal, customer, and third-party audit management - Environmental Health and Safety (EHS / HSE) management SBS Ground Control - Employee training management (LMS) - Self-Paced training - Document control SBS Asset Tracking Database - Calibrated equipment control - Preventive maintenance - Asset inventory management SBS Inspection Database - Record incoming material, in process, and final product inspection data - Generate real time SPC charts - Inspection plans and Control Plans - Archive data for further statistical analysis SBS Vendor Management - Maintain an approved vendor list or AVL - Develop vendor / supplier qualification plans - Maintain vendor / supplier qualification history Modules may be purchased separately or in any combination.

SimplerQMS offers a cloud-based Quality Management Software, specifically designed for the Life Science industry. SimplerQMS helps ensure compliance with various regulatory requirements, including FDA 21 CFR Part 11, EU Annex 11, GxP, cGMP, GAMP 5, GDPR, EU IVDR & EU MDR, ISO 13485:2016, 21 CFR Part 820, and ICH Q10, among others. The system is fully validated according to GAMP5. The system offers a range of Life Science QMS modules such as Document Control, Change Control, Training Management, Supplier Management, Complaints Management, Non-Conformance and Deviation Management, CAPA Management, Audit Management, Technical Documentation Management, Risk Management, Quality KPIs and more. SimplerQMS integrates with Microsoft Office and allows users to work with documents in applications such as Word, PowerPoint, and Excel. Overall, SimplerQMS delivers efficient, paperless workflows that align with the compliance requirements of the Life Science industry.

Qualityze EQMS Suite is a next-generation Enterprise Quality Management Software. It is specifically designed for businesses to efficiently manage their quality processes, customer expectations and compliance requirements. It helps them address operational challenges so they can achieve excellence in terms of quality, safety and reliability. It comes with pre-defined templates for controlled documents, audit checklists, regulatory forms, material compliance reports and many more. Qualityze EQMS Suite is a set of 14 integrated modules that help create a closed-loop system to manage end-to-end quality from anywhere. Our range of smarter quality solutions is built on the Salesforce.com technology platform. These modules are Nonconformance Management, CAPA Management, Document Management, Change Management, Audit Management, Training Management, Supplier Quality Management, Inspection Management, Customer Complaints Management, Material Compliance Management, Forms Management, Permit Management, Calibration Management, and Maintenance Management, Forms Management and Field Safety Management. Our Quality Management solutions help create a culture of quality and continuous improvements by proactively mitigating quality issues.

FMEA is critical in avoiding risk and minimizing quality cost. DataLyzer FMEA offers DFMEA, Process Flow, PFMEA and Control Plan and they are all linkedin avoiding time to synchronize the steps. From Control Plan the SPC setup can be automatically created. Many features are available like reference or Foundation FMEAs, different criteria or classification sets, full authorization, Document and issuing control, Action management, Ballooning import, Automatic translation, Reporting, ITAR configuration etc etc DataLyzer FMEA saves a lot of engineering time avoiding repetitive work. DataLyzer FMEA closely follows the methodology defined in VDA AIAG and RM13004. DataLyzer FMEA can link to DataLyzer SPC software.

BPAQuality365, a QMS software, can be used in your secure Microsoft 365 cloud. It leverages tools used daily by collaborators and does not require you to change your user habits. It is modern, compatible with all devices, adaptable to your specific needs, and powered through innovative M365 technologies. The app includes powerful compliance document management, audit, non-conformance, CAPA action, process and process maps, incident, change, risk, FMEA, SWOT, equipment, health, safety, environment modules compliant with ISO 9001, FDA Part 11 and medical regulations. The QMS app integrates with Teams discussions and users can ask the QMS while chatting in Teams and share QMS card with their colleagues. You can go further to achieve your Quality 4.0 goals by combining powerful AI features with best-in-class workflow automation and business intelligence. BPA's Microsoft Preferred status allows you to customize your QMS to meet your needs, share knowledge with your power users, and learn about M365 technologies.

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

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.

Artintech ERP is a comprehensive enterprise resource planning solution designed to optimize and streamline your business operations across various departments. Tailored for small to medium-sized enterprises (SMEs), Artintech ERP offers robust functionality with a user-friendly interface, allowing businesses to seamlessly manage their resources, inventory, human capital, finances, and customer relations all in one integrated platform. Why Choose Artintech ERP? * User-Friendly Interface: Designed for ease of use, Artintech ERP minimizes the learning curve, ensuring a smooth transition and quick adoption across your organization. * Cloud-Based Flexibility: Access your ERP system anytime, anywhere, with our secure cloud-based solution, which provides the flexibility to manage your business on the go. * Comprehensive Support: Our dedicated support team is available to assist you every step of the way, from initial implementation to ongoing maintenance and updates.

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.

EHS Insight, an EHS management platform, empowers organizations to ensure compliance across the company. EHS Insight is affordable and easy to set up. It provides businesses with all the tools they need for managing incidents, audits, inspections, compliance obligations and corrective actions. EHS Insight offers exceptional support for businesses both during and after the software implementation.

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

Quality Planning Studio FMEA software integrates core quality tools and ensures compliance to fundamental process flow steps. FMEA software is a single integrated software tool that can be used to plan, document, and monitor core quality requirements. It has been synonymous with continuous improvement programs for manufacturers around the world. The strong inter-relationship between Process Flows, FMEA and control plan, as well as SPC, is evident. FMEA ensures that products, processes and detection techniques are continuously improved. SPC results are continuously fed back to the engineers responsible for the FMEA process. Quality Planning Studio FMEA software stores all data in the QPS database. This ensures traceability and integrity across your plants' Process Flow/FMEA/Control Plan information. QPS can communicate with DataMetrics' SPC software (DataMetrics), which allows you to reduce redundancy, monitor characteristic capabilities, and more from the Control Plan.

A web-based software suite for medical device companies that automates their processes and simplifies regulatory compliance. Modules include Audit Management, CAPA and Complaint Handling. Designed from the start for ISO 13485 compliance and 21 CFR Part 11 compliance.

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

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

Audit Manager is a software that supports quality management. It allows digital management of audits and quality controls in all phases: planning, compilation, and collection of evidence through checklists; verification and management for the entire nonconformity process; definition of corrective measures and data monitoring. You can access the calendar to schedule audits and add the relevant information (subject, checklists, lead auditor, coauditor or participants) for each one. Staff, both internal and outside, can be invited via email to consult the audit schedule prepared directly from the app. Once the inspection has been completed, you can generate the audit report as a PDF or Excel file and share it with the Company Management. You can add the archived minutes to the company's document repository.

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

ZEBSOFT GRC & ISO management platform is a holistic approach for managing Governance, Risk & compliance. ZEBSOFT's intuitive web interface makes it easy to manage ISO standards (9001, 14001 and 22301), 27001, 27001 and 45001 and many others. ZEBSOFT has powerful integrated modules for Risk, Quality, Environmental, InfoSec, Compliances, policies (templates included) & documents, equipment & asset management with maintenance/calibration/testing planning. Improve internal communication, assign ownership, plan, and conduct audits. To see the full potential of ZEBSOFT, book a demo today!

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

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.

It is difficult to monitor quality risks without a robust system of knowledge management. You need processes to efficiently identify, capture and manage critical documents and information. Sphera's FMEA Pro software provides a configurable framework to support different FMEA methods and specialized capabilities in risk data management, so you can be sure that the right controls are in place. It links quality information across the design and manufacturing process to help you achieve quality that your customers expect. Sphera's FMEA Pro software helps you improve your bottom line by implementing an efficient, standardized method to analyze risks. Sphera's enterprise Advanced Risk Assessment software helps companies identify, assess and manage the impact of operational risks.

SoftExpert FMEA, an enterprise software, helps companies manage Failure modes and effects analysis. SoftExpert FMEA uses a proactive approach to anticipate defects before they happen, allowing companies the assurance of quality in their delivery. FMEA is applicable to different contexts, such as products, departments, assets and processes. It can also be used to reduce the engineering workload and improve machines and resource availability by identifying, analysing and improving high-risk parts. The solution monitors continuously failures identified by FMEA. It shows reports and charts that include indicators such as severity and risk priority. These highlight causes at any given moment. The solution increases product reliability and safety, while increasing customer satisfaction.

Panotica Hydra, a modular QMS software, is designed to manage quality processes in accordance with ISO 9001, 14001 and 18001 standards. The software allows you to not only gather all the company's improvement processes into one system but also to integrate all employees on the platform. Hydra allows remote supervision of activities that aim to improve quality and engage employees in the improvement process.

Document Management Software automates office work, collaboration, document flow and business processes. The planning of quality control processes for incoming or outgoing goods reduces inspection time and optimizes cost. Assists in the maintenance of equipment. Assign tasks to be completed, take notes and keep track of them. Corrective action, 8D, GAP Analysis, Kaizen Proposals, FMEA, Ishikawa diagrams. Job Descriptions, Personnel Records and Announcements. Standardize audits checklist. Records of system audits. 5S Inspections. Software to manage MSDSs creation and management.

MediaLab's Intelligent Quality Engine (IQE) solution is designed to deliver powerful automation for laboratory non-conforming event management processes. IQE eliminates the need for paper-based, manual investigation and CAPA processes while reducing cost and supporting the quality improvement program. IQE helps your laboratory follow corrective and preventive action standards as outlined by CAP, joint commission, ISO, and other accrediting bodies. You'll benefit from a streamlined approach that supports your regulatory compliance. Start by using our online form templates, or create your own. Allow employees to create events as problems arise. MediaLab will route your event through each phase of the event management lifecycle, from initial event description to risk analysis, closure, and change effectiveness evaluations. Your current processes and forms work beautifully in IQE.

FactoryQA is a quality management software that can be used by manufacturers. Software Features 1. Management of Non-Conformance/CAPA 2. Document Control 3. Instructions for Work 4. Inspection sheets 5. Audits 6. Analytics Services: 1. ISO Certification Consultants 2. Workshops for ISO Certification 3. Fractional Quality Management Services

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.

AutoDCP allows you to link projects or select operations from different projects into one larger composite project. This is useful when you want to combine purchased parts, different components, or generic operations with part-specific data. These types of composite projects automatically update when the underlying data changes. AutoDCP is the most cost-effective and fastest way to maintain a linked Process flow diagram, FMEA, and Control Plan. FMEA creation is easy and quick with Risk Profiles. FMEA drag/drop is simple and easy to use. AutoDCP has many features that will greatly speed up your efforts. These are some of the key features that make it much easier to create and maintain FMEAs or Control Plans.

Software for quality management. We offer QM solutions for all quality issues. This is what we have been doing for over 25 years. Our modular software BabtecQ is a complete solution to quality management. We are quality specialists. Babtec Qube is a cloud-based platform that allows you to connect with suppliers and customers to manage your quality tasks. Our products enable you to show the entire range of quality processes within and between companies. This is quality you will love sharing.

We make the world safer, more sustainable, and more productive. Our software analyzes data from many sources to help companies make better strategic business decisions regarding mitigating risk. This is called Integrated Risk Management 4.0 (IRM 4.0). Our success is based on the fact that we have never had to deal with any of these incidents. Sphera's Environment, Health, Safety & Sustainability solutions provide end-to-end risk management on a single platform that can be scaled to meet companies' daily and strategic EHS&S goals. Sphera's Operational Risk Management Solutions help operators create a unified strategy to drive Operational Excellence throughout the enterprise. Sphera's Product Stewardship Solutions combine the best-of-breed and rich content to allow you to comply, streamline, and automate all aspects of your products' lifecycle.

Digitize your processes. Security. Environment. Qualitative. Hygiene. Of Business. Centralize. Simplify. Automate. All your tasks can be managed with one tool. Your organization's sustainability and performance. Automated processes are the foundation of safety and performance. BlueKanGo is the digital EHSQ platform to manage them. BlueKanGo is the digital EHSQ solution that has been trusted by over 3500 customers for 18 years. Digitize your Quality, EHS, and other processes. Quality and audits management. Employee safety and health. Environment. CMMS & inspection. Certification, Standards. Corporate Social Responsibility (CSR). Regulatory Watch. Strategic Planning. 6 key differences that make BlueKanGo different. BlueKanGo has been around for 18 years and is the SaaS platform with no boundaries. BlueKanGo is an innovative, scalable, and all-inclusive solution

These proven solutions will help you operationalize your pandemic response plan, monitor and report on your employees' and visitors' health, and increase your business' productivity. Engage employees, improve workflows and increase data visibility at all levels of your company to improve safety culture. Cority helps you to break down silos within departments, improve reporting, achieve operational excellence, and increase productivity. Cority's unified compliance management system is designed to take the guesswork out compliance. myCority connects your frontline employees, no matter their location, with the tools they need in order to reduce risk and drive compliance. EHSQ experts develop, implement, and support the Cority solution. We are the industry leader in Occupational Health, Industrial Hygiene and Employee Health solutions. You can take your safety programs to the next step by proactive mitigating risks, managing compliance and reducing incidents.

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.

Cognidox is an online document-management system for high-tech, life sciences and medical device product development. Cognidox is available in the cloud and as an on-premise solution. It promotes product lifecycle management and knowledge sharing between developers and clients, partners, customers, and customers. Cognidox is secure and reliable. We offer plug-ins for many programs, such as Microsoft Office. We also offer an API that allows you to integrate almost any process with Cognidox. Cognidox's core function is a DMS. An add-on for Cognidox allows you to license and distribute documents to third parties via a fully sandboxed website. This allows you to publish specific documents while keeping your main storage secure. Another popular add-on is gBMS - Graphical Business Management System. Visio can be used to capture your business processes. A good BMS should give clear oversight of your entire operation.

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

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

Experts and moderators love the PLATO software SCIO™. PLATO e1ns, a web-based software, is recommended for easy handling by all members of the engineering department. It includes the most important SCIO™ functions. PLATO e1ns allows for optimal product development process (PDP) design. PLATO has created e1ns to help in the early stages. You lay the foundation for cost- and risk-avoiding. SCIO™,-FMEA's database technology fulfills the requirements for knowledge management, multi-user capability, and foreign language support. SCIO™,-Matrix is a fast method for system analysis. It's used to convert customer requirements into product functionality through optimal implementation. Complete documentation and planning of each step. Securely stored and available for retrieval in SCIO™.

Risk management integrator. Knowllence provides software, training and consulting services to help you manage QSE risk effectively. You can manage the safety of your employees (single file, arduousness, and chemical risk). Manage your robust design process (functional analyses, FMEA FMEA and FTA). You can manage the robustness and industrialization of your plant (AMDEC Process FMEA monitoring plan). Control the risks associated with ISO 14971 and design of medical devices. We can adapt our software to your requirements and follow your processes and standards. We can provide a complete service to assist you in your work sessions and risk studies. This will allow you to move your project forward while also making it sustainable. You keep control over the study and the plans for actions with efficient and simple-to-use software.

You now have the option to be your own Quality Management Expert via an online platform. To facilitate smooth processes, templates can be integrated into your company. We offer complete Quality Management Systems as well as online solutions for ISO 13485 Medical Devices, and ISO 9001 General Quality Management.

Small to medium-sized businesses (SMEs) will love the cloud-based Quality Management System software (QMS). TRACKMEDIUM, a monthly subscription service, includes modules such as Audit Management, CAPA and Document Control, Management of Change (NCM), Training Management, and Management of Nonconformance Management. TRACKMEDIUM allows companies to create safer products, increase efficiency, and comply with industry standards such as ISO 9001, 14001, and OSHA while lowering costs. The Audit Management software by TRACKMEDIUM streamlines audit-related tasks. This includes creating standard audit and checklist templates and generating audit plans. It also allows for the generation of audit recommendations and tracking CAPAs through closure.

Quantum's Qavach system offers live dashboards and automated alerts. Real-time tracking and comprehensive tools will help you achieve HSE goals while reducing administrative burdens. Manage risks, report non-conformances and streamline documentation. Audits that are effective can reduce quality costs and improve shareholder satisfaction. Our prevention-focused system allows you to benefit from proactive actions and minimized cost. Demonstrate these features.

All the information you need to test specifications, supplier communications and test failures, as well as lab notifications, corrective action, and performance metrics, is at your fingertips. LINK Services is a Product Compliance Testing program management software that focuses on product and material conformity. It provides tools for supply chain partners to communicate tasks and analytics related to product and material test programs and specifications, test orders, lab reports, corrective actions and bills of materials and related product quality management activity. LINK bridges the gap between brand/retailer enterprise system (e.g. PLM, ERP/SAP), vendors, and analytical testing labs (in-house and third-party). It harmonizes and centralizes data into a single, lab-agnostic, system.

Rapidly Transform Your Compliance, Quality & Risk Management Systems in Today's All Digital, All-Remote World. Predict, Mitigate and Automate Compliance Monitoring in Real-Time. Always be prepared for compliance inspection

QSE SMART is an application for quality, safety and environmental management that was specifically designed for small to medium-sized businesses and projects with 5 to 500 users. QSE SMART is a solid framework that complies to key requirements of ISO9001 and 45001 and simplifies the daily running of your integrated QSE management software. QSE SMART makes ISO practical for your business. QSE SMART is based on a risk-based approach to ISO 31000. It helps you to identify and exploit key information and metrics that support your business goals in regard to quality, safety and environmental management. This includes your objectives and targets as well as management reviews, risk and opportunities, audits, inspections, management reviews, management reviews, risk and improvement, audits, inspections, audits and inspections.

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.