Hubicus Quality Monitoring Alternatives

Perfect for a small company, TLM has everything you need, and can accelerate the implementation with consulting, training, procedure templates, and document writing/coaching support, plus we have validation templates and a system setting mode so small medical device companies have special features to help manage technical files and 510K submittals. TLM QMS Software saves you money AND makes your QMS more effective by providing a dual technology landscape for the two distinct QMS user types. Core modules include: • Audits • Contact Manager (CRM) • CAPA • Customer Feedback • Document Management • Electronic Forms • Employees • Employee Feedback • Equipment Calibration • Evaluations • FMEA • Inspections • Inventory/parts • Library • Meetings/Reviews • Metrics • Projects • Purchase Orders • Quality Record Mgt • Rejected Materials • Risk & Opportunities • Sales Orders • Strategic Planning • Surveys • Tasks/Events • Training • Work Orders

QVscribe, QRA's flagship product, unifies stakeholders by ensuring clear, concise artifacts. It automatically evaluates requirements, identifies risks, and guides engineers to address them. QVscribe simplifies artifact management by eliminating errors and verifying compliance with quality and industry standards. QVscribe Feature Spotlights: Glossary Integration: QVscribe now adds a fourth dimension by ensuring consistency across teams using different authoring tools. Term definitions appear alongside Quality Alerts, Warnings, and EARS Conformance checks within the project context. Customizable Configurations: Tailor QVscribe to meet specific verification needs for requirements, including business and system documents. This flexibility helps identify issues early before estimates or development progress. Integrated Guidance: QVscribe offers real-time recommendations during the editing process, helping authors effortlessly correct problem requirements and improve their quality.

The SBS Quality Management Software Suite (QMS Suite) is a group of 5 software modules that work together for efficient Quality compliance. The QMS Suite can be deployed on your local server or accessed from our cloud server. Each module is designed for ease-of-use to reduce training overhead and improve overall compliance. Password controlled access and privileges ensure you may control access to critical features for each user. The SBS QMS Suite of modules: SBS Quality Database - CAPA / 8D with root cause analysis - Nonconformance management - Risk analysis (FMEA, SWOT, risk register) - Audit management SBS Ground Control - Employee training management (LMS) - Document control SBS Asset Tracking Database - Calibrated equipment - Preventive maintenance SBS Inspection Database - Data collection / SPC - Control Plans SBS Vendor Management - Approved vendor list / AVL - Supplier qualification plans Great product for efficient and affordable QMS Compliance.

With ARMATURE Fabric™ you can manage your accreditation, certification, credentialing, audit, quality, and compliance activities within a single platform. Our software enables you to save time, operate more effectively and securely, and better serve your stakeholder communities. Whether you are managing institutional, programmatic, or specialized accreditation programs; certifying individuals, products, or organizations; conducting audits or assessments; or resolving non-conformances or other issues, ARMATURE Fabric can make it easier and more efficient for you and your stakeholders. Our secure, cloud-based software allows you to collect data in multiple ways (through online applications, audits, assessments, self-evaluations, inspections, forms, and surveys); manage your accreditation, certification, audit, and compliance workflows; capture and manage documents and artifacts, identify and remediate issues; generate reports; and spot new trends.

The [FP]-LIMS modules are based on a powerful SQL database solution. These allow a quick query and processing of data. We guarantee maximum user-friendliness! Our job server is a central element for the automation of functions, which executes time- and event-controlled tasks. Like, to automatically monitor limit values and the associated alarm message (e-mail, message on the monitor, etc.) when they are exceeded. Using modern LIMS software and modules such as analysis management, inspection planning, workflow management, or ERP, you can design your quality management in the best way. This makes your production processes more efficient.

The first step is measurement. We find that clients regularly monitor the customer service delivered by their people by listening to calls or reviewing chats or Twitter and Facebook posts. The results are often saved in spreadsheets and after a few weeks this becomes so burdensome to reliably and effectively mine for information that the quality program fails. OptiOp allows you to easily create and maintain your evaluation forms; perform evaluations quickly and simply across any number of skills or media channels; meet with employees and give feedback and record and track action items; measure the turnaround time for giving feedback and close the loop with employees signing off on receiving feedback. Use the chatbot to request a demo. The benefits don't stop there - for maximum effect, measurement and feedback must be applied consistently so OptiOp allows you to perform calibration sessions efficiently, bringing your evaluation or quality assurance team together.

Zeva provides a highly intuitive interface and utilizes Microsoft’s Azure Cloud to provide a robust and secure hosted environment to scale from small organizations with fewer than 10 users to global enterprises with over 10,000 employees. What makes ZEVA a value proposition, for any organization, is the ability to create and manage an unlimited number of custom assessments, while providing real time data and analytics to decision makers and management anywhere in the world. Mitigate risk and maintain compliance with centralized secure hosting, improved reporting, and real-time dashboards and analytics. Items identified with “Findings” can be immediately assigned corrective measures to ensure timely remediations. The CodeLynx team developed the ZEVA platform to support the evolving evaluation requirements of commercial and government organizations of any size.

Modify the fields based on the reality of your company. Grant permissions and define your deadlines. Take control of Documents. Evaluate your suppliers. Generate a SWOT Matrix. Create Corrective Action Status reports. And everything that the ISO Standard requires. Get reminders of due deadlines and notifications every time you're assigned a task; by email and on the panel. Record comments and versions for better follow-up. Includes change history. It maintains a history of creation, edition, derivation of the collaboration processes. Planning, registration and monitoring of processes, audits and procedures. Attach evidence and documentation. Optimization of time, cost reduction, visualization and interaction of processes, methodologies for follow-up, timely resolution of problems. These are just some of the benefits of digitizing your management system with inblue QMS.

Proven solutions to operationalize your pandemic response plans, systematically monitor, and report on the health status of your employees and visitors, and assist your business’ return to productivity. Improve your safety culture by engaging employees, enhancing workflows, and increasing data visibility across all levels of your organization. Cority helps you break down departmental silos, improve reporting, and achieve operational excellence. Cority's unified compliance management solution is designed to help you take the guesswork out of compliance. myCority connects your frontline employees no matter where they are with the tools they need to mitigate risk and drive compliance. EHSQ experts design, implement and support the Cority solution. That’s why we are the leader in Occupational Health, Industrial Hygiene, and Employee Health solutions. Take your safety programs to the next level by proactively mitigating risks, managing compliance, and reducing incidents.

Audit Manager is the software supporting quality management that allows digital management of audits, quality controls and tests in all their phases: planning and compilation through checklists, collection of evidence and field surveys, verification and management of the entire nonconformity flow, definition of corrective actions and data monitoring. Access the calendar and schedule the audits by associating the relevant information with each one (subject, checklist, lead auditor, co-auditor, participants, etc.). The staff involved, both internal and external, can receive an invitation via email and consult the prepared audit schedule directly from the app. Once the inspection is completed, generate the audit report in PDF or Excel and share it directly from mobile with the company management or managers. The archive of all minutes is always available and organized and you can add it to the document repositories used by the company.

Eliminate manual, repetitive tasks so you can focus on delivering safer, more effective products – faster. IQVIA’s SmartSolve Postmarket Surveillance is your complete, SaaS approach for postmarket surveillance (PMS) and provides best practices for centrally managing all post market surveillance activities. Fusion is a SmartSolve and RIM Smart user event that provides an in-depth education into timely and relevant quality and regulatory topics with actionable insights and practical tools that can be applied within any Life Sciences organization. Fusion started as a live SmartSolve user conference and has evolved over the past couple of years to include virtual and live events for both SmartSolve and RIM Smart users. Simplify, automate and integrate your compliance response times, accuracy, predictive planning and efficiency with IQVIA SmartSolve™ Regulatory Connector. Connected Intelligence is our innovative, interconnected approach that helps to drive operational efficiencies.

Empower your supervisors, trainers, Quality Assurance teams, and agents to optimize customer interactions. Review live-monitored and recorded calls, and synchronized voice and screen recordings via a user-friendly interface. Automatically analyze interactions for actionable insights. Enhance service quality, determine call-handling effectiveness and confirm agents are adhering to scripts and processes, all with a sophisticated call center quality management software. Easily manage team performance via intuitive interface. Listen, watch, evaluate and score agents, and deliver effective coaching and e-Learning. Provide packaged call content with e-Learning resources to coach agents and improve KPIs with instant, relevant, and regular feedback. Easily, efficiently and quickly perform evaluations. Prepare agents to excel by providingin-depth performance reporting.

Is your quality management program working? Screening a small percentage of calls may leave non-compliant interactions hidden, and risk fines, lost business or worse. Verint can help. Most contact centers only review between 1 and 3% of calls. This severely limits your ability to identify risks and manage quality and compliance. Verint Automated Quality Management can automate the whole quality management process and help you achieve better compliance. Evaluate calls, identify non-compliance and assign coaching—for 100% of voice and text interactions. In this way, you will quickly gain a new level of insight into your organization’s standards of service and compliance. This helps you identify employees that need coaching to improve, and reveals any procedural steps that cause compliance and/or quality issues.

Select from a menu of preformatted questionnaires or configure from a pool of 700 industry-relevant questions. Select content to meet your corporate requirements. Deploy question sets that match contractor category, risk rating or other criteria. Flexible functionality at the desk-top. Expired contractor certificates mean risk. CQN provides expert document management and verification services that reduce exposure and ensure due diligence. Gain corporate peace of mind with class-leading certificate monitoring and automated notifications. CQN evaluation of health, safety and environmental systems ensure your contractors have achieved industry standard requirements for HSE management. Contractors receiving CQN Advanced approval have demonstrated compliance with high-value HSE systems, maintain critical coverages and have industry-leading performance.

Install Efficient QMS™ online quality system anytime on your Company's website or install eQMS on a webhost server that you create using modern freeware. After eQMS installation, your Company's Admin is required to approve Users before they can login. Efficient QMS™ needs a license to operate. Its important for you to browse to your eQMS files to open the temp "license.txt" file with a text editor then find the expiration date. Visit with our tech support before the temp license expires to get a permanent license that enables uninterrupted operation of eQMS. The solution is very cost effective because "Lite eQMS" is complementary for any business in the United States and low cost "Complete eQMS" enables your Company to immediately implement an online quality system. Evaluate Efficient QMS™ document control and quality control software program to see how it can dramatically improve the efficiency of the management system that your Company needs to keep your Customers happy.

PROLab is software used for planning, organizing, performing, and analyzing interlaboratory studies. It is used for both proficiency tests assessing the performance of laboratories (typically acc. to ISO 13528) and collaborative studies for the validation of analytical methods (typically acc. to ISO 5725: 1‐6). PROLab specifically provides all necessary features to meet the requirements of ISO/IEC 17043 on quality management and quality assurance for proficiency testing providers. The regular validation process includes both automated and manual testing to ensure that reports, computations, and displays of charts are done so correctly. With respect to the statistical evaluation of data, PROLab conforms to the computational requirements outlined in the standards listed. Tools for the performance assessment of laboratories across PT rounds. With PROLab, data entry and management are both easy and flexible. Data entry is possible by means of a flexible data import module.

Improve incoming parts quality and supplier quality performance,reduce the risk of production interruption, optimize the total cost of ownership, and manage supply chain risks. Monitor the in process quality performance and change of the trend through the whole flow of production, take preventive actions to reduce failure rate. Manage and control the quality of to-be-shipped out products, improve product competitiveness. Customer focus. Quick response to customer complaints, Improve the service and quality, improve customer satisfaction. Record and follow up corrective action and preventive actions.Realtime display of the task progress of each member.Enhance the capability of continuous improvement and improve corporate quality management system. Reduce the time on preparing audits, Improve the efficiency and effectiveness of audits. Mechanism in place to facilitate the audit as scheduled to be compliant with the requirements and regulations.

Delivering Quality Management Software to help manage your compliance against ISO standards. Such as ISO 9001, ISO 13485, ISO 17025, FDA, GMP, BRC. EQMS software is being placed into many different companies within different industries and with different ISO requirements with an overarching goal of helping in achieving product quality and optimum standards. Some EQMS applications are better suited as enterprise quality management systems and other systems for small to medium-sized businesses however regardless of setting, below are some key points that components of any of the best quality management software out there. Businesses may implement a quality process like CAPA (Corrective Action Preventative Action) into their EQMS software and this process may look different from one business to another even if they belong to the same sector. The ability to customize the workflow, fields, layouts to adapt to the behaviour of the business ensures a smooth implementation.

Plex Quality Management System (QMS) helps process and discrete manufacturers meet strict industry and customer compliance with a closed-loop digital system of record. Ensure predictable, repeatable quality delivery through in-line quality, clear reporting, and simple audit tracking. Meet industry compliance and customer regulations with quality documentation available in real-time, digitally, across the enterprise. Drive new and repeat business growth with on-time delivery performance, improved supplier management, and increased customer satisfaction. Making quality management inherent to your workflows and processes reduces quality loss and risk of warranty issues or recalls, improving your brand reputation and customer relationships. With Plex quality requirements and documentation are available and shared in real-time across the enterprise. Plex helps you generate process control plans with detailed inspection instructions and digital checksheets.

WinSPC is a real-time statistical process control application that helps manufacturers create the highest quality product for the lowest possible cost -- collecting and analyzing real-time shop-floor data from virtually any source. Dashboards combine real-time statistics, charts, and events into grids to summarize current plant or line performance. WinSPC empowers monitoring. Detect process change and deliver actionable intelligence. WinSPC real-time control charts on the shop floor, enable anyone to immediately detect and process issues. Close the quality loop from "detection-to-correction" with built-in triggers that alert, or take action for you, when violations occur. Experiment, visualize and reveal more about any variable or relationship using the one-click variable analyzer. Quickly create, publish, and share quality reports throughout your organization using a graphical report builder with dozens of standard report templates.

QMS enables companies to eliminate paper-based quality management process while adhering to compliance and regulatory standards. QMS not only increases operational efficiency but also increases compliance to set quality standard. QMS brings all of your quality processes together in one place by integrating related processes and actions to enable better analysis and process improvement. QMS has been vetted and found compliant with CFR 21 Part 11 guidelines by USFDA and the European Regulatory Auditors, amongst others. Benefits Single platform to manage all related processes Reduce expensive mistakes Evidence for educated decision making Credibility improvement Improved customer satisfaction

Quality Management Software. Overcome the challenges of Quality in your company with the software rated as the easiest to use. More than 45,000 professionals are already simplifying their management systems. Ask questions about Qualiex via Online Chat. In addition to email and phone, you can chat in real time with ISO 9001 Lead Auditors during our office hours, taking questions quickly and conveniently. Non-Compliance Management. No more feeling lost in the non-conformity process. Forlogic Tracker will eliminate spreadsheets, automate the charges made by email, centralize your information and evolve your NC management. Be more efficient in dealing with non-conformities by managing the main causes. Looking back, we can see that Quality has undergone several transformations. We have already lived through the era of Inspection, the era of Statistical Control and then Total Quality Management.

iCompliance is a comprehensive digital platform designed to streamline Quality, Health, Safety, and Environment (QHSE) management, Environmental, Social, and Governance (ESG) initiatives, and Governance, Risk, and Compliance (GRC) processes for organizations across various industries. Our software offers tools for incident reporting, risk assessments, audit management, corrective actions, and more to ensure compliance with regulations and standards, promote safety and environmental responsibility, track ESG performance, engage stakeholders, and manage regulatory requirements, internal controls, and risk mitigation strategies. With customizable workflows, real-time analytics, integration options, mobile accessibility, and multilingual support, iCompliance empowers organizations to achieve operational excellence, mitigate risks, and drive sustainable growth.

Paradigm 3 is a web and desktop-based platform designed to aid businesses in compliance management in regards to Document Control, CAPA Compliance, and Competency Tracking and Training. The software offers tools such as an event manager for incident investigations and customer complaints, tasks delivered by e-mail, audit preparations, among others. Some of the industries that benefit from Paradigm 3 are Healthcare, Manufacturing, Test Labs, and Service Industries. With Paradigm 3 it is no longer necessary to buy endless add on modules to manage all your compliance needs. Our system is made up of 4 modules with over 50 standard forms to meet all of your requirements for Quality, Safety and Environmental and by utilizing our form designer you can create new forms or redesign the ones supplied to ensure they exactly meet your needs.

Monitoring Performance. Recording Results. Contact us to get access to a demo account, or to set up your organization. Download 80/20 Quality from the Apple App Store, Google Play, or use our web app. Customize the dropdown menus to meet your needs. Inspectors on the floor can document a non-conformance directly in the 80/20 Quality App with enough detail and pictures to illustrate the issue for the decision-makers in your business. Management receives an alert that an issue has been identified and can make a decision on what steps manufacturing should take to fix, scrap or return a non-conformance. The inspector is alerted through the app with explicit instructions on how to move forward. The inspector takes the approved action and documents its completion. All activities are logged for data capture and analytics to look for trends and find improvement opportunities.

In a food manufacturing business, buyers, production, technical and quality staff all need to work as a TEAM to produce profitable, safe, and high quality food products. 3iVerify is an affordable, secure, cloud-based food safety management system that helps technical, quality and compliance managers tame the tidal wave of processes, procedures and paperwork that they deal with every day. We achieve this by having a simple, logical approach to key processes like supplier and material approvals management, supplier monitoring, document management and corrective action management. We believe that life is too short for spreadsheets and paperwork. We always work with our customers to ensure their system is bespoke and tailored to their specific business model. We can offer you only the modules you need, so you don't need to waste money on stuff you wont use. For further information please visit our website for a comprehensive introduction to the solution we offer.

Effivity is a cloud-based / on-premise QHSE/FSMS/ISMS software to implement a robust Quality - Occupational Health & Safety - Environment Management System & offers 100% conformity to ISO 9001, ISO 14001, ISO 45001, ISO 22000, HACCP standards. Effivity makes ISO compliance simple, easy, quick, value adding, cost-effective, collaborative and time-saving which results in enabling an organization to enhance efficiency and augment productivity as validated by users in more than 120 countries. Effivity offers a unique approach to optimize your management system with world-renowned QMS software, HSE software & FSMS-HACCP software. Simplicity, standardization and customer satisfaction delivered with no-code quality management system software, safe workplace enabled with 100% customizable occupational health & safety management system, sustainable environment possible with a user-friendly environment management system and safe food delivered with HACCP software that is ready to use.

Isolocity is the complete front to back solution for GMP and ISO 9001 cannabis compliance in the industry. Our software marries the principles of GMP and ISO to the management and documentation of your production seamlessly. Isolocity's compliance management software is built with GMP principles in mind. All modules are essential to improving safety and yield at your facility allowing you to get certified with ease. Isolocity makes ISO 9001:2015 compliance simple by automating labour-intensive processes. Isolocity's QMS software helps you improve consistency in production and guides you through your ISO 9001 certification. Isolocity’s risk management module includes planning with HACCP and PFMEA. Easily plan, initiate, and prioritize actions to minimize hazards and failure in your production. Our tablet-friendly solution manages inspections while providing the quality manager reports in real time. Isolocity provides full traceability from customer to supplier.

Document control made simple, document lifecycles, create, review/approve, revise, and retire documents. All transactions are recorded with e-signatures and timestamps and stored in the Audit Trail. Audits from start to finish. From audit planning to audit preparation and all the way to audit closure, track and document your internal and external audits with the SOLABS QM10 Audit APP. Intuitive reporting because trending and tracking are so critical to any quality management system, the SOLABS QM Essentials package includes advanced reporting capabilities. The reports and dashboards are available in formats that are easy to use, customizable and share the most common formats, whether it be Excel, PowerPoint, PDF, etc. with anyone within your organization. Create, assign, schedule and monitor training in a few clicks. Leverage online assessments to validate your team’s learnings. The SOLABS QM Training section allows you to handle all aspects of training.

EzyPro Adaptive Management system (QHSE) is a powerful way to integrate compliance, performance, and continuous improvement. EzyPro QHSE, a one stop solution for compliance, maintenance, and operational control. Increase efficiency, share information, and collaborate. Its modular approach offers flexible subscriptions according to needs. EzyPro Healthcare - Hospital Quality Management system with integrated action tracking and dashboards for meeting requirements such as NABH and JCI. designed as a centralized hub for continuous improvement throughout the Healthcare unit. Option available for remote consultancy service for implementation support. Comprehensive maintenance management solution bundled for the first time with QHSE Management system. Extend equipment lifespans, improve time efficiency and equipment uptime resulting in reduced costs and increased profits. With a QR code assisted asset retrieval, easily manage work orders for repairs, maintenance or transfer of assets.

Software & Services that keep the workplace safe, compliant, and your employees well trained. For more than two decades, SMG has been a trusted partner for process management, improving workplace safety, and ensuring OSHA and other regulatory compliance on local, state, and federal levels for businesses ranging from food service distribution centers and restaurants to LTL freight carriers. SMG’s software-driven expertise in health and safety management empowers your business to easily ensure compliance, reduce costly incidents, and improve operations and logistics. Replace generic policy documents and overlooked safety plans with action- driven software tools that seamlessly integrate with processes for training employees, conducting safety audits, reporting incidents, and taking corrective action.

Create and manage documents online, preventing misplaced printed copies and lack of organization. Gather all information in one place and make it easy to monitor and address nonconformities. Define, collect, and analyze KPIs through comparative charts, to help you with decision making. Plan and implement actions to address risks and opportunities in a simple and controlled way. Overcome spreadsheets and printed copies. Get file control in a cloud base with 24/7 access from any location and device. Optimize document elaboration, review, and approval. Manage access permissions and automatic notifications about document changes and expiration dates. Have always the most recent versions of all files uploaded into Genebra. Do not waste time browsing through numerous spreadsheets, and never lose revisions of your documents.

Are you a quality or risk manager looking for a powerful solution? With ISO2HANDLE, you gain superpowers that give you control over your quality, safety, HR, and environmental processes in no time. ISO2HANDLE is the perfect solution for businesses in virtually any industry. Our software supports capabilities such as risk management, resource management, complaint management, task management, risk assessment, registrations, notifications, document management, audits, onboarding, evaluations, expense claims, leave requests, environmental measures, and more. With just one click, you can generate reports, making audits a breeze. Based in the Netherlands, we proudly support hundreds of companies worldwide.

AQF is a management software of quality developed by professionals in quality control. AQF is a total solution that makes it possible to eliminate the procedures paper and it helps you to easily carry out all the stages of the actions in quality assurance. We offer a modular service to allow all companies to obtain a suitable product while avoiding unnecessary costs. Only the main module is mandatory for the installation of the additional modules. Our AQF module is not only complementary to its own modules. The AQF module is also complementary to the software and/or ERP already used by your organization. Create, manage and share your controls internally, your supplier's audits, your procedures, and your documents. Simplify procedures between users and assign specific rights to control outgoing information. Automate the request for documentation in order to avoid oversights. With the Internet of Things (IoT) connectivity, manage and control the temperature and humidity.

Rapidly Transform your Compliance, Quality & Risk Management Systems for Today’s All-Digital, All-Remote World :Predict, Mitigate, Automate and Monitor Compliance in Real-Time. Be Always Compliance Inspection Ready

FlinkISO Quality Management System is one of the best quality management softwares available for small and medium business. Integrated with ONLYOFFICE editors, FlinkISO QMS allows you to build Custom HTML forms as per your QMS document's requirement. You can build your own QMS without any expert help or coding. To start with, modules like Audit Management, Customer Complaints, Document Management, Change Control etc are already in-built in the application. You can add your custom business rules, email triggers and even additional HTML fields with drag-and-drop feature. Application is available, both on-premise & on-cloud with flexible and affordable payment options. While on-cloud, you get 45+ days of evaluation period without making any payments, on-premise edition is available at USD80/mo.

AURA is a web based QMS software that helps organizations to effectively monitor and manage your quality compliance activities. We bring you organization-specific quality management system and enable you to streamline your quality process for better risk management and assured compliance. With aura audit management software, you can maintain quality standards specific to different business areas within the enterprise.

QEdge QMS for Enterprise Quality Management Software (EQMS) system that optimizes the quality of various processes and ensures regulatory compliance. Enterprise Quality Management Software (EQMS) system reduces the risk of quality process failures; lowering overall costs and making the organizational processes more compliant. QEdge, as an EQMS accommodates companies in a disciplinary regulatory environment to make Quality Management System more robust and well managed by bringing all the quality processes such as Change Control, Deviation, Investigation, CAPA, Market Complaints, OOS, OOT, Risk Assessment, Document Control activities, Training Records and many more on a single platform. QEdge is an intuitive and highly configurable software platform to manage various regulatory, and nonregulatory business processes that facilitates error-free, cross-functional communication and collaboration with Quality management as a base and can interface with the legacy systems.

To bring new products to market as quickly as possible in compliance with global regulations, organizations need to standardize and automate their business processes that manage the collection, tracking and analysis of information and the resolution of related issues. QUMAS EQMS (formerly ProcessCompliance) is a cloud-based solution for Enterprise Quality and Process Management that delivers comprehensive integrated regulatory, quality and compliance management capabilities in a validated QMS environment. QUMAS’s data-centric approach allows you to flexibly manage quality content and to access and re-use all quality data, providing comprehensive visibility into Quality. QUMAS’s interactive quality dashboards provide QMS overview across business areas and quality initiatives. Reports are available for export, email and scheduling. QUMAS allows QMS departments to exchange information securely, efficiently and compliantly in the cloud.

Quality Planning Studio FMEA software integrates the core quality tools and ensures adherence to fundamental process flow steps. It's a single, integrated software tool for planning, documenting and monitoring core quality requirements.For manufacturers worldwide, FMEA has become synonymous with continuous improvement programs. Process Flows, FMEA, control plan and SPC have a strong inter-relationship. The FMEA process ensures that products, processes or detection techniques are constantly improved. Continuous feedback is provided from SPC results on the shop floor to engineers responsible for the FMEA process. Quality Planning Studio FMEA software stores all data within the QPS database, ensuring traceability and integrity of your Process Flow/FMEA/Control Plan information across your plants. QPS can also communicate with our SPC software (DataMetrics), allowing you to reduce redundancy and perform characteristic capability monitoring from the Control Plan.

1factory's Manufacturing Quality is a cloud-based and on-premises quality control software solution specifically created for manufacturing companies of all types and sizes. Powerful, reliable, and secure Manufacturing Quality by 1factory provides first article inspections, factory monitoring, quality control plans, in-process and final inspections, incoming inspections, inspection management, CAPAs, non-conformances, and more. Additional key features include running metrics calculations for Process Performance (Pp, Ppk), Process Capability (Cp, Cpk), variation / SPC control management, defect-risk monitoring, and more.

Harness your data from your toolchain to create high-performing engineering and quality teams. neuro provides complete visibility of your engineering and quality performance. Close the gap between insight and action to increase velocity. Set user-defined goals to track progress, identify roadblocks, and align engineering and quality teams with business priorities. Deliver consistency across your portfolio. Address the challenge of managing dependencies among teams, especially third parties. Provide rapid reporting across your tool stack. Smart dashboards provide greater insight and remove administrative overhead with automated reporting. neuro delivers across enterprise, digital, and agile landscapes to transform engineering, product, and quality management. We help leaders eliminate waste, realize value, and align decisions with business priorities and goals to deliver results. Fast integration to optimize your existing tool stack.

Maintaining consistent product quality and quality processes can be challenging in today’s pharmaceutical manufacturing environments. Regulated industries such as the Pharmaceutical, Biotech and Life Sciences are required to maintain Good Manufacturing Practices (GMP) to meet regulatory requirements. Not only do you need to meet GMP requirements you must also be able to prove this. Using paper-based forms, disconnected systems, or manual processes to manage, track and report on quality issues and actions does not provide effective solutions for implementing harmonized, integrated quality management processes, which follow industry best practices.

Systematic Safety Management, Compliance Monitoring and Quality Management are not only a legal requirements for commercial air operators but also increase the efficiency of the organization, save money and thereby make the operation more profitable.If you still manage your safety, compliance and quality requirements using generic software tools and paper-based processes, you are missing out on significant efficiency savings that an electronic solution like Qperfect IAMS can realize.

RizePoint is a top-rated brand, quality, and safety compliance management software designed to help businesses manage the entire quality process--from audits to automated corrective action. RizePoint gives businesses a comprehensive view into their compliance data by integrating the RizePoint Mobile Auditor app and cloud-based Management Console in one platform. The solution is suitable for companies in the food, hospitaliy, and retail industries.

Greenlight Guru’s Medical Device Success Platform is the only all-in-one solution that helps you get your products to market faster, with less risk, and advance your success in-market. The platform helps companies manufacture safer products and get to market faster, simplifies regulatory compliance, and provides a single source of truth by connecting the management of all product development, regulatory, and quality processes from documentation and design controls to submission and ongoing compliance. Device makers across the globe are replacing reactive quality management tools and shifting their focus and efforts to ensure successful product launches and in-market success of innovative, life-changing devices.

BITqms, software for your quality management. The professional software for your quality management BITqms, the quality and management software offers you optimal support for all processes in your company and facilities. From document management, audit or risk management to inspections, tests or action management. Whether stationary or on the go via app, with our software for quality management BITqms you always have your tasks and processes under control. The most flexible software in quality management. With BITqms, the structures of your organization can be mapped exactly as they actually are. Structures, responsibilities and processes are flexible and can be individually defined. Always close to the customer. From advice on the sales process to support with the implementation in your company, to support from our support team - we are always happy to answer any questions you may have. Independently suitable for every area.

We help our customers produce safer, more sustainable food through supply chain and farm management software that delivers insights, drives better decisions and enables collaboration across global supply chains. Modernize your quality management by capturing product quality, process, facility and safety checks into a cloud-based solution. Providing a secure and easily accessed location for all your due diligence and quality data capture. Digitize every step of your product quality journey from raw material to end product. Incorporate third-party data sets and overlay A. I principles to optimize and steer inspection resources, improving utilization. Ensure the accuracy of labels through automated template recognition eliminating product recalls. Identify key risks and highlight required action to improve customer satisfaction, improve shelf-life performance and drive out waste. Centrally build quality attributes you wish to measure.

Arena’s product-centric quality management system (QMS) software enables medical device manufacturers to deliver safe and compliant products to market fast. Arena QMS streamlines new product development and introduction (NPDI) by connecting quality and product processes. Arena QMS ensures regulatory compliance to quality standards and regulations including FDA 21 CFR Part 820, Part 11 and ISO 13485. Arena QMS enhances visibility and traceability by controlling quality processes in context with bills of materials (BOMs), SOPs, DMRs, DHFs, specifications, drawings, and training plans.

Quarta EVO the web-based Quality Management software for Quality Assurance and Compliance , based on a workflow engine. It allows you to digitize the Quality system and monitor processes at any time and from any place, efficiently and integrated through an internal dashboard and KPIs . The QMS solution to manage and improve the performance of Quality and Safety Management Systems in companies; built on a powerful Workflow engine , it combines high functional completeness with web-based architectures and technologies, all oriented towards intra- and inter-plant collaboration and measuring process performance . The Quarta suite is simple, fluid and intuitive; able to collect data in real time, analyze them, organize them and automatically create a series of indicators that allow you to keep the entire Quality System under control.