Alternatives to CampaignQA

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

Verify Technologies helps you to stay compliant with food safety legislation. Verify Solutions is a paperless, integrated food business management platform that offers fully integrated quality, sales and purchasing management features. Verify is a software designed for small and medium manufacturing companies. It helps them to increase efficiency, reduce operating costs, improve their quality control, and automate HACCP and Food Traceability 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.

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

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.

IQM Studio is our technology that powers our Integrated Quality Management process. It's made up of our IQM Modeling, and IQM Scripting features. IQM Modeling's powerful test generator algorithm can automate test design in our Cause Effect Models. This takes the guesswork out testing. You can save time and ensure that you are validating system behavior by writing test cases using a model of your system. IQM Scripting can be used in a standalone mode to create automation scripts using keywords. You can also combine both features with IQM Studio to generate automation scripts from your model. IQM Scripting allows everyone in a project to create automation scripts. This includes non-programmer resources such as BA's and SME's.

It can seem like a never-ending series of tradeoffs to bring breakthrough products to market within highly regulated industries. MasterControl's GxP software simplifies workflows, so you don't have to compromise quality for cost or innovation with regulation. Complete and connected meets flexible and fast. MasterControl Quality Excellence transforms quality data and processes to a competitive edge. Modern software is the first step in modernizing your manufacturing operations. MasterControl Manufacturing Excellence, from work orders to production records (EBR/eDHR), to logbooks and work instructions, is the easiest way to digitalize manufacturing.

Quality Management Software that helps you manage your compliance with ISO standards. ISO 9001, ISO 13485 and ISO 17025 are some examples. EQMS software is used in many industries and for different ISO requirements. The goal is to improve product quality and maintain optimum standards. While some EQMS software is better suited for enterprise quality management systems, others are more suitable for small- to medium-sized businesses. However, there are key components that all quality management software should have. Businesses can implement a quality process such as CAPA (Corrective Activity Preventative Action), into their EQMS software. However, this process may look different for each business, even if they are in the same industry. It is possible to adjust the workflow, fields, layouts to suit the business's needs. This ensures smooth implementation.

Businesses that are growing need to be able to react quickly to changes in the market. Customers and suppliers expect quick responses to critical questions. Companies that are slow to respond lose sales. A management software suite is essential for any company that wants to make a mark in their industry. A Quality/Assurance Management System is a set of business processes that are focused on meeting customer requirements and achieving quality policy. QIT Consulting's Enterprise Quality Management Software was developed by quality consultants and ISO auditors. It is fully configurable and customizable web-based quality management software. We are confident that we will provide the best quality software products and services that will exceed your expectations. We will refund your purchase price if you are not completely satisfied within 60 days. No questions asked.

PROLab software is used to plan, organize, perform, and analyze interlaboratory studies. It is used to perform proficiency tests that assess the performance of laboratories (typically acc. It is used for both proficiency tests assessing the performance of laboratories (typically acc. to ISO 13528) as well as collaborative studies for validation of analytical methods. to ISO 5725: 1-6. PROLab provides all the features required to meet the requirements for ISO/IEC 17043 quality management and quality assurance for proficiency testers. Regular validation includes both manual and automated testing to ensure that computations, reports, and displays of charts are correct. PROLab adheres to the listed computational requirements for statistical evaluation of data. Tools for performing laboratory performance assessments across PT rounds. PROLab makes data entry and management easy and flexible. A flexible data import module makes it possible to enter data.

Organizations need to standardize their business processes and automate them in order to bring new products to market quickly and comply with global regulations. QUMAS EQMS (formerly ProcessCompliance), a cloud-based solution that provides integrated regulatory, quality and compliance management capabilities within a validated QMS environment, is QUMAS EQMS. QUMAS's data-centric approach lets you manage quality content easily and access and re-use all data. This gives you a comprehensive view into Quality. Interactive quality dashboards from QUMAS provide QMS overviews across all business areas and quality initiatives. Export, email, and scheduling are all possible for reports. QUMAS allows QMS departments the ability to securely, efficiently, and compliantly exchange information in the cloud.

Food Portal makes it easy to comply with auditable scheme requirements. It's simple and makes your job much easier. Food portal allows you to operate extremely robust integrated quality systems in a fraction of what it costs to use traditional offline methods. Superior systems make your life easier and your food safer. Compliance requirements are increasing in importance. Food Portal provides the solutions you need to support food manufacturers. Food Portal's systems automate repetitive tasks so that you can concentrate your attention on what is most important. Food Portal is more than a compliance tool. It actually helps to speed up quality processes and make them less demanding.

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.

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

TIPQA is a tool that companies use to make continuous and measurable improvements in customer service, productivity, profitability, and customer service. Our QMS software allows industry leaders and managers to monitor compliance and manage quality throughout their supply chains. TIPQA QMS Software will support best practices in quality management and help you create a comprehensive continuous improvement plan for your company. Numerous companies who require high-quality products and strict quality control have found success with the TIPQA quality management software. TIP Technologies is more experienced in complex business processes within regulated manufacturing environments than any other solution provider. TIPQA's quality management solution allows users to be flexible, adapting to changing markets and quality demands. TIP Technologies is constantly improving its quality management system.

Caliber's Integrated Quality Management Platform - EPIQ stands apart from other generic quality offerings on the market. Caliber provides seamless quality management by integrating and functionalities across departments in a way that is unmatched. This platform also provides capabilities that go beyond the regular quality management requirements. It can be used to build foundations for quality metrics, performance analytics and CPV. Automation is a major investment for many companies. However, there are still inadequacies when it comes to information sharing between departments. Quality Assurance departments must see the effects of deviations across all departments. Many planned and unplanned changes must be reviewed and closed by more than one department. Interdepartmental transactions are a key part of risk mitigation.

FlinkISO Quality management system is one of the most popular quality management softwares for small and medium businesses. FlinkISO QMS integrates with ONLYOFFICE editors. This allows you to create custom HTML forms according to your QMS document's requirements. You can create your own QMS with no coding or technical knowledge. Modules such as Audit Management, Customer Complaints and Document Management, Change Control, and Change Control are already built into the application. Drag-and-drop allows you to add custom business rules, email triggers, and additional HTML fields. Flexible and affordable payment options are available for both on-premise and cloud applications. On-cloud users get 45+ days of free evaluation, while the on-premise edition costs USD80/month.

ZipQuality, a software-enabled medical device service, helps companies bring new products to the market. Our collaboration platform allows agile teams to make rapid design changes while maintaining regulatory compliance. System (processes and tool) pre-configured; no need to change your quality system. The integrated system is able to handle rapid design iterations in product documentation. Your team will be guided by experienced consultants at every stage. Software tools that are fully featured, scalable, and built on the powerful ENOVIA platform. Our integrated system allows for rapid design changes, while keeping data and documentation in sync. All records are maintained in a audit-ready condition. Product requirements, Hardware requirements, Software requirements. We have a deep understanding of complex, software-intensive devices. ZipQuality is a structured documentation system that supports good systems engineering and efficient risk management. It also provides clear traceability.

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.

Food Safety Software allows for cost-effective transformation in food safety, NPD and customer complaints, as well as supply chain transparency. Our food safety software includes VACCP/TACCP and horizon scanning to help you save time and complete consistent, auditable risk assessment of suppliers and products. You will never be audited in non-conformance and you can be audit-ready 24 hours a day. Transform specification management for raw materials and finished products, and answer customer queries instantly. Automate supplier quality monitoring and internal non-conformance management using automated workflows. This will ensure that non-conformances are promptly closed. Our team will manage all complaints using market-leading software. This will save you time, money, and improve customer service. You can launch new products faster and better together, while still meeting all safety, legality, and profitability requirements.

We all know that a system must be accessible in order to be used. You don't want pages to load and searches to take too long. You want to be able add records or find the information you need quickly, wherever and whenever you want. Wismatix QMS allows you to do exactly that. Wismatix QMS was built on years of experience in quality management systems implementation and auditing. It is known for its speed and reliability. Wismatix is committed to providing exceptional customer service. You will receive full support for the use and maintenance of your online quality management system. In the event that you do not require our system, we will send your data to your server to allow you to upload your data. Wismatix is committed to providing exceptional customer service. Wismatix will provide you with full support for the use and maintenance of your online quality management system. In the unlikely event that you do not require our system, we will send your data to you to upload to your own server.

CamLine can create LineWorks MES, a powerful Manufacturing Execution System that is tailored to your production needs. The LineWorks Suite has all the essential functions you need. Your path to a custom-made MES is based upon proven and continually improved software products that have been around for many years. You can add individual requirements to the software by creating use cases. They are the best practices for increasing efficiency and quality. These best practices have been repeatedly optimized over many decades. You get an agile solution that can adapt to your production's future needs. You choose an infrastructure solution that has proven itself to be durable over many years.

Software for compliance management in the cannabis industry. Optimized Cannabis Compliance Software. The medical marijuana industry is highly regulated. Most states require that cultivators, distributors, and processors keep track of every ounce of cannabis, as well as any edibles they sell or throw away for quality issues. You must keep a record of all transactions, from cultivation to final sale, in order to be compliant with the law in the cannabis industry. The constant changes in the medical marijuana market, along with the need for compliance and risk reduction, cannot be managed using traditional software or manual templates. The Features You Need to Be Successful. Otter Systems Compliance Management Software is a central platform that tracks regulatory requirements, organizes compliance documentation, and manages compliance processes. Features include: Cannabis Document Control; Policy Management; Change Management; Supply Chain Control.

digiQC empowers Site Engineers with a Construction Quality Management Software solution. A quality management system in construction can help you take control, increase visibility, and increase accountability and quality standards across your Quality Assurance team. You can keep an eye on your onsite projects without compromising the quality. Get insight and spot alarming issues before they exceed your budget or project deadlines. Your quality assurance team can record data digitally using a mobile app and a web platform. You can reduce the amount of paperwork and human error that goes into manually filling out data forms. You can create a process that ensures that quality checks are completed at each step. Your site engineers should be able to take and record real-time data during quality checks.

Cetec ERP is a cloud-based manufacturing enterprise resource planning solution that caters to small and medium sized businesses. As a full suite ERP, it helps manufacturing companies to manage the various business processes specific to a manufacturing environment, including bills of materials, quoting and job costing, supply chain management, inventory control, procurement, shop floor management, and quality assurance. The intuitive nature of a web-based platform makes Cetec ERP easy to learn and implement, and keeps costs significantly lower than ERPs with similar breadth of functionality. Cetec ERP is more operations-focused than traditional ERPs, and adds value to SMB manufacturers with modern technology, user friendly interfaces, real-time data, strong cost accounting, and a fully integrated workflow. While nimble as a platform, the breadth of features caters to manufacturers in electronics contract manufacturing, high mix/low volume, aerospace and defense, medical device OEMs and contract manufacturers, machine shops, industrial equipment OEMs, cabinet manufacturers, fabric, and more. Services are offered on a monthly subscription basis that includes support via email, phone and through other online resources.

TraQtion has worked closely with some of the most innovative food companies in the world. These case studies will show you how TraQtion helped these companies stay ahead of their competition. TraQtion supplier management software reduces supplier-driven quality defects or recalls by standardizing supplier approval processes, scoring risky facilities, and enabling end to end document tracking. Nearly 20% of the U.S. food supply comes from overseas. You need to monitor supplier performance in order to be FSMA- and FSVP-ready. TraQtion uses scorecards and supplier metrics to encourage supplier reviews that are data-driven. You can create a supplier network that includes all your top performers.

QMS allows companies to eliminate paper-based quality control processes while still adhering to regulatory standards and compliance. QMS not only improves operational efficiency, but also increases compliance to established quality standards. QMS combines all your quality processes into one place. It integrates related actions and processes to facilitate better analysis and process improvement. QMS has been vetted by the USFDA and European Regulatory Auditors and found to be compliant with CFR 21 Part 11 guidelines. Benefits All related processes can be managed from a single platform Reduce expensive mistakes Evidence to support educated decision making Credibility improvement Improved customer satisfaction

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

Secure Audit, Risk, Compliance, Quality Software. Available in both Cloud-based and On-Premise deployment options. Auditrunner provides granular encryption and role-based access controls for audit files and documents-at-rest. All data is protected. Our platform has automated over 3000 business processes for companies around the globe. These are just a few examples of the GRC platform modules. Cloud-based and On-Premise. Just deploy and begin using. The platform's seamless integration allows you to start enjoying the benefits within weeks of launch. The platform's low-code design allows for customization and compliance with any standard or regulation. You can operate in a fast-moving, constantly changing regulatory environment and comply instantly with a multitude of different legislation without assistance. Our ease of use is unmatched.

Your supervisors, trainers and Quality Assurance teams can empower your agents to improve customer interactions. A user-friendly interface allows you to review recorded and live-monitored calls and sync voice and screen recordings. Automated analysis of interactions to provide actionable insights. A sophisticated call center quality management system will help you improve service quality, assess call-handling effectiveness, and ensure agents adhere to scripts and processes. Use an intuitive interface to manage your team's performance. You can listen, monitor, score, and evaluate agents. Then, you can provide effective coaching and eLearning. To coach agents and improve KPIs, provide e-Learning resources and packaged call content. Perform evaluations quickly, efficiently, and easily. Agents can excel with in-depth performance reporting.

Modify fields to reflect the realities of your company. Give permissions and set deadlines. Take control of Documents. Evaluate your suppliers. Create a SWOT Matrix. Create Corrective Action Status reports. All the other requirements of the ISO Standard. You will be notified by email or on the panel of due deadlines and notifications whenever you are assigned a task. For better follow-up, record comments and versions. Includes history of changes. It preserves the history of creation, edition, and derivation of collaboration processes. Planning, monitoring, and registration of processes, audits, and procedures. Attach documentation and evidence. Optimizing time, cost reduction, visualization, interaction and interactivity of processes, methods for follow-up, timely resolutions of problems. These are just a few of the many benefits of digitizing your management systems with inblue QMS.

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.

One platform for compliance, risk management, governance. GRC gives you and your colleagues an overview and helps you to manage and document your compliance, risks management, and ongoing control. The process is simplified and everyone involved needs to know only one system. This increases efficiency. No matter what industry you work in, there are regulations and standards you must adhere to and documentation that proves it. It is a complex project for many. Complex legislations and many requirements make it difficult to get support from the rest. Compliance will not be easy. However, RISMA's solution may make compliance simple so you can focus on what you are good at.

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.

Greenlight Guru is the only product development and quality management platform designed specifically for medical device companies. The Medical Device Success Platform helps companies get safer products to market faster, simplifies FDA and ISO regulatory compliance, and provides a single source of truth by connecting the management of all quality processes like CAPAs, risk, audits, document control, training, design control, and more. Device makers across the globe are replacing their outdated paper-based and general-purpose legacy quality systems with Greenlight Guru to push beyond baseline compliance and achieve True Quality.

All your test management activities can be managed in one collaborative environment. Our unified testing platform allows you to use any type of testing tool, methodology, or team. Small groups can benefit from a single environment that allows for rapid team organization. You can quickly start projects using pre-defined templates, which are flexible and easy to customize. Enterprise QA departments have unlimited project management options. They can use pre-defined templates, which are very simple and quick, and a variety of automated and manual testing activities. All of this while keeping everything in synch. All your test management needs can be met quickly by centralizing all testing activities in one central repository. This allows you to ensure quality and multi-directional traceability.

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.

Next-generation software quality management platform combines automated and manual testing. Your TestOps will help you improve product quality control and increase productivity of your QA and development teams. We understand that software delivery is complicated for both QA and development teams. Allure TestOps is a quality management platform that seamlessly integrates with all of your frameworks and keeps all testing data centralised and transparent. Allure TestOps enables your team to connect manual and automated testing, increasing their productivity. You can speed up your CI/CD process and gain instant insight into your test coverage. Allure TestOps can update your test documentation based upon test run results tracking, analysis and analysis. No more excuses for test cases that are no longer relevant.

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.

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.

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.

QEdge QMS is Enterprise Quality Management Software (EQMS). It optimizes quality and ensures regulatory compliance. Enterprise Quality Management Software (EQMS), reduces the risk for quality process failures, lowers overall costs, and makes organizational processes more compliant. QEdge is an EQMS that allows companies to manage their Quality Management System in a disciplinary regulatory environment. It brings together all quality processes, such as Change Control and Deviation, Investigation and Market Complaints. OOS, OOT and Risk Assessment. Document Control activities, Training Records, and Document Control activities. QEdge, an intuitive and configurable software platform, allows for cross-functional communication and collaboration. It can interface with legacy systems and facilitates error-free, cross functional communication.

Effivity is a cloud-based or on-premise QHSE/FSMS/ISMS program that helps you implement a robust Quality – Occupational Health & Safety – Environment Management System. It conforms to all ISO 9001, ISO 14001 and ISO 45001 standards. Effivity makes ISO compliance easy, quick and cost-effective. It also allows for collaboration and time-savings. This is validated by more than 120 countries.

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.

Arena's product-centric QMS software allows medical device manufacturers to quickly bring safe and compliant products to the market. Arena QMS connects quality and product processes to streamline new product development and introduction (NPDI). Arena QMS ensures compliance with quality standards and regulations, including FDA 21 CFR Part 820 Part 11 and ISO 13485. Arena QMS improves visibility and traceability by monitoring quality processes in context of bills of materials (BOMs), DMRs and SOPs, as well as specifications, drawings and training plans.

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

In today's pharmaceutical manufacturing environment, it can be difficult to maintain consistent product quality and quality processes. To meet regulatory requirements, industries like the Pharmaceutical, Biotech and Life Sciences must maintain Good Manufacturing Practices (GMP). You must not only meet GMP requirements, but you must also be capable of proving it.

Ennov Quality Suite. A comprehensive QMS to increase efficiency and ensure compliance. Ennov Quality Suite Ennov Quality Suite combines the power of Ennov Doc and Ennov QMS with Ennov Report and Ennov Training to create an integrated quality management solution that improves operational efficiency and ensures compliance to industry standards like 21 CFR Part 11, GxP, and ISO. Ennov Quality offers a predefined inventory that includes quality documentation, processes, and workflows. These are based on industry standards and best practices. Ennov Quality customers can quickly get their system in production and begin to realize their return on investment. Ennov Quality, as all Ennov solutions, is easy to set up and requires no IT skills. A unified and intuitive content and information management platform that supports and enriches the entire Life Sciences product cycle. Our comprehensive QMS improves operational efficiency

Quality AnalytiX® allows operators, quality personnel and manufacturing engineers to view SPC data and other parameters that impact product quality. Any of the many built-in SPC calculations can be applied to any process variable. Users can also integrate SPC data into logic and expressions to drive corrective action based on process trends. Quality AnalytiX uses ICONICS Hyper Historian™ technology to collect data and calculate. The architecture is able to support large enterprise-wide SPC Quality Programs as well as applications that require rapid sample rates. Quality AnalytiX allows you to spot trends and make informed decisions based upon real-time SPC data. Using built-in graphs, charts, and alarm views, you can reduce scrap and increase production yields. The powerful workflow technology can initiate control actions based upon quality conditions or alarm violations and provide changes to process equipment like PLCs, temperature controllers and DCS systems.

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.