Qualios Alternatives

isoTracker Quality Management is a popular cloud-based quality management software (QMS) that is used by small to medium sized businesses on a worldwide basis. It helps to manage ISO 9001, ISO 13485, ISO 22000, ISO/IEC 17025, ISO 14001, ISO 45001, ISO/TS 16949, ISO 14971 systems...plus many other systems. It also conforms to the requirements of 21 CFR Part 11. It is a flexible and modular product with modules in document control, audit management, non-conformance management, customer complaints management, risk management, training management and CAPA management. It can be configured to meet an organization's specific needs and provides free training and free support. It has been independently judged to provide the best customer support in its category.

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.

BPAQuality365 is a prebuilt QMS software to use in your secured Microsoft 365 cloud, leveraging tools used by collaborators daily, with no need to change user habits. It’s modern, compliant with any device, flexible to match your unique needs, and powered by innovative M365 technologies. The app includes powerful compliance document management, audit, non-conformance, CAPA action, risk, equipment, health, safety, environment modules compliant with ISO 9001, FDA Part 11 and medical regulations. The QMS app is closely integrated to discussion flows in Teams and enable instant quality improvement. Go a step further and reach your Quality 4.0 objectives by combining powerful AI features, best-in-class workflow automation, business intelligence and mobile Power Apps to run on any device. Benefit from BPA’s Microsoft Preferred status to configure your QMS to your needs, transfer knowledge to your power users and get trained on M365 technologies.

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.

Logistics, Manufacturing & Construction Companies that comply or are planning to comply with several industry standards such as ISO9001, ISO45001, ISO14001, ISO22001, ISO27001 etc Qooling helps companies to build better, safer, and more secure products & services. The platform allows you to easily gather information from production plants or sides through the easy-to-use interface for the people in the field. This gives companies the ability to really leverage the data to improve the company. Qooling allows organizations to improve their safety, quality, and security by using data. All the tools are available on one platform, allowing you to improve safety culture and quality. Continuous improvement is only possible with everyone's efforts. Easy-to-use tools make it easy to engage employees. Your personal desktop is dynamically created based on what you value. This ensures that you only see the information that is urgently needed.

Xybion LIMS (formerly Labwise XD) is an all-inclusive LIMS, ELN, QMS, and DMS. Xybion LIMS drives lab workflows, instills consistency, improves data quality, and supports regulatory compliance with a complete laboratory management solution that connects with your operating systems with powerful laboratory information management and analytics. Xybion LIMS creates optimized workflows for the unique business needs of all regulated laboratories including research, diagnostics, quality control, stability studies, and more.

Qualtrax is a complete quality and compliance software system used to manage and control documentation, automate key business processes with customizable workflows, streamline training management, manage internal and external audits and ensure critical industry regulations are addressed in real-time. Qualtrax is an invaluable resource in heavily-regulated industries, where complying with standards including ISO 17025, 17020, 13485, and 9001, TNI, GFSI, FDA, and FQS is required.

Qualio is an all-in-one quality and compliance management platform built for small and growing businesses in life sciences and healthcare. Reliable, affordable, and easy to use, Qualio helps companies building life saving products get to market faster by reaching 100% ISO, GxP, and FDA compliance. With Qualio, companies can conveniently manage document control, training, CAPAs, NCRs, audits, suppliers, complaints, and more in one platform.

QSE SMART is a quality, safety, environmental and risk management software application developed especially for small to medium-size business organizations and projects of 5 to 500 users. QSE SMART provides a solid framework that complies with key requirements of ISO9001, 45001 and 14001, and simplifies the day-to-day running of your integrated QSE management system. QSE SMART makes ISO make sense in your business. Designed around a risk-based approach according to ISO 31000, QSE SMART helps you to capture and exploit the key information and metrics that support your business objectives in respect to quality, safety, environmental and business risk management including your objectives and targets, management reviews, risks and opportunities, non-conformances and improvements, audits and inspections, accidents, incidents and hazards, corrective actions, equipment calibration and control of documented information.

Cloud-based Quality Management System (QMS) software that is ideal for small to medium businesses (SMEs). TRACKMEDIUM is a monthly-based subscription service with modules including Audit Management, CAPA, Document Control, Management of Change, Nonconformance Management (NCM), and Training Management. TRACKMEDIUM enables companies to create better and safer products, improve efficiency, and achieve compliance with industry standards including ISO 9001, 14001 & OSHA while lowering costs and risks. TRACKMEDIUM's Audit Management software streamlines audit-related tasks which include creating standardized audit and checklist templates, generating an audit plan, conducting audits, identifying nonconformances and recommendations, tracking CAPAs through closure and reporting results.

Panotica Hydra is a modular QMS software for managing quality processes according to the requirements of ISO 9001, 14001, 18001 and other similar ones. The software allows not only to gather all of the company’s improvement processes in one system, but also to actively integrate all of the employees on the system platform. Hydra provides access to supervise activities remotely aimed at improving quality as well as engages company’s employees in the improvement process.

The SBS Quality Database is a simple, inexpensive, ISO 9001 compliant software program that allows small businesses to efficiency manage the Quality Management System or QMS. The database tracks corrective actions, preventive actions (CAPA), internal audits, safety improvement, supplier corrective actions, continual improvement projects. Compile and analyze Customer Survey results. Identify and minimized risk using the risk management module (FMEA & SWOT analysis) . Document QMS review meetings and results. Document interested parties as part of the Context of the organization. Use the dashboard for a quick view of the overall performance. Cloud based or locally installed options are available. The program is ideal for small businesses striving for ISO 9001:2015, API Q1, AS9100, or TS16949 compliance. Free demo downloads are available from our website so you may try before your buy.

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.

Drive exceptional quality and process performance with a platform that puts you in cruise control. Crush poor quality, safety concerns and redundant processes with the all-in-one E-Data Now!® Audit and Quality Inspection platform, that includes the tools you need to connect your team performance, simplify checklists, root cause non-conformance, improve processes and grow customer satisfaction. E-Data Now! is a leading manufacturing, construction and site safety/compliance no-code, cloud-based platform, that digitizes quality inspection and process audits, automates workflows and provides mobile data-driven insights. The obvious benefit – clearing out your paperwork, cleans up the clutter in your audit processes and identifies unknown audit redundancies. The simple answer – a custom form creation and mobile data collection platform with digital tools made for the trades: to train, record, capture, react, correct, schedule, comply and build better processes.

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.

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. At qmsWrapper, we cater to each industry’s unique quality management needs with tailored features: Compliance Made Easy: Adhere to standards like ISO 13485 and ISO 9001 effortlessly, maintaining a robust QMS. Risk Management: Simplify risk assessment with ISO 14971-compliant tools, effectively mitigating risks. Document Control: Intuitively manage documents for enhanced traceability and version control. Cloud-Based Accessibility: Access your QMS anytime, anywhere. Electronic QMS: Embrace efficiency with digitized QMS for faster approvals and real-time updates. Audit Management: Prepare for audits confidently with scheduling, tracking, and reporting tools.

From now on, you can get all the needed documents simply and easily without losing valuable working hours and for a very lucrative price! Subscription is simple, just a few clicks will get you to the purchase subscription screen. Enter company data, organization name, logo, and information about the procedures approver. Fill in the forms & implementation according to the ISO 9001 requirements as shown on the screen. Retrieve controlled reports and forms with the name & logo of the organization. Ready for the external audit. Self-preparation in your free time and without the need for intervention of an external party. The system is accessible year-round, and data can be entered into the system at any time. Avoid last-minute haste! Everything needed for a quality management system, including producing controlled forms with your company logo on them. Get everything you need for the external audit & your ISO quality management system in one convenient place.

myQualityTM is an online ISO 9001 quality management system portal designed for quality practitioners and consultants. Contains a comprehensive set of required documented information ready for assessment, design, implementation, certification and ongoing support. Learning the basics is quick and easy. Learning how to really harness the full, powerful potential of the software will take a little more time and be part of your continuous improvement strategy. Buying the software, receiving the training and calling it good is like buying a computer only for internet access. You need to learn how to make it a real, worthwhile investment. Luckily we provide a full suite of 'How To's' with our Tech Support for everything else. The platform includes the minimum documented information requirements through intuitive, interconnected databases, registers, templates, forms, procedures and much more. A once-off setup fee includes a dedicated company domain, x5 managers, unlimited users, etc.

ZEBSOFT GRC & ISO management software platform is a holistic approach to managing Governance, Risk & Compliance. With an intuitive and easy to use web interface, ZEBSOFT makes to easy to manage ISO (9001, 14001, 22301, 27001, 45001) and many other standards. 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 carry out audits. Book a demo today to see what ZEBSOFT can do!

QUALIPRO is a management software of quality, environment, occupational health & security and food safety. Assistance, study and consulting quality, environment, health and safety at work, HACCP. Training and awareness-raising in the field of quality, environment, health and safety at work, food safety and audit techniques. Thanks to its setting flexibility and specific modules QUALIPRO responds perfectly to the expectations of the Pharmaceutical and medical devices industry. QUALIPRO is fulfilling the requirements of “Good Manufacturing Practices, GMP” and ISO13485 standards. QUALIPRO, Quality / SHEQ software, is aligned to major global standards including ISO 9001, EN 9100, ISO IATF 16949, ISO 14001, ISO 17025 and ISO 15189, ISO 22000, IFS, ISO 13485, ISO 27001, ISO 45001 standards. QUALIPRO is an innovative and modular software, it is an efficient tool for a Quality / QSE / SHEQ / SHE management system.

Save Money, ensure quality and great talents with uQualio - the most affordable and easy-to-use Video Learning Platform. With uQualio, you can create Online Video Learning courses to educate and train your employees, sales partners, potential customers, or end users. Qualio solves a wide range of business and industry needs to enable you to create and scale the content you require to educate others. Create Video Learning courses quickly and easily from anywhere, anytime. With real-time tracking and analysis, you can easily measure user performance on custom dashboards. Communicate with your users with instant and efficient messaging on the platform. uQualio is your all-in-one learning system, customized by you for your business needs.

Designed and validated by our SPC / Six Sigma consultants, this is one of the most versatile and economical software for analyzing statistical process control (SPC) data. It can also compute the six sigma process metrics as well as predict the process average for Engineering Process Control (EPC). A must for all organizations and students pursuing Six Sigma. Our management consultants have vast experience in successfully implementing ISO9001:2015 / ISO14001:2015 / ISO17025:2017 / ISO22000:2018 / ISO27001:2013 / ISO45001:2018 / ISO50001:2018 / SA8000:2014 Management Systems at various client organisations around the world. On the basis of their experience, our consultants have prepared step-by-step system implementation guidelines that provide clear directions to managers (management representatives) who would plan and implement the system. Following these guidelines could cut down the cost and duration of your project substantially.

Virje complies with the requirements of 21 CFR Part 11, 21 CFR Part 820, and ISO 13485. Overwhelmed by the thought of Part 11 software validation? Accessible from wherever you are, for whenever you work. Eliminate paper, reduce cost, and increase efficiency with automation and centralized collaboration. Perfect for small to medium-sized businesses. Built from the ground up specifically for medical device quality management. A system that is flexible enough to adjust to your workflows and processes, without having to compromise. Configurable change order approvals by employee role and by document type. Notifications to responsible personnel at every stage in the change process. Ability to designate material dispositions for individual documents. Easy access to released and historical versions of documents. Quick viewing of document change history. Tracking of where-used locations and distributed hard copies. Periodic document review notification.

OpenText™ ALM Quality Center serves as the single pane of glass for software quality management. It helps you govern application lifecycle management activities and implement rigorous, auditable lifecycle processes. Leverage the reusability, traceability, and automation of ALM tools to improve efficiency in developing, testing, and maintaining applications. Automate result collection and gain real-time visibility into application quality, eliminating time-consuming and error-prone human processes. Enforce standard process with built-in ALM workflows and templates. Ensure compliance with detailed change tracking and a risk-based approach. Build an automated, vendor-neutral ecosystem for data consolidation across your application lifecycle with out-of-the-box integrations and APIs. Meet your scalability, security, and application architecture requirements with the deployment option of your choice – on-premises, cloud, or SaaS.

The eInfotree™ Quality Management System delivers a unified approach to Enterprise Information Management by linking data and business processes in a highly intuitive manner. This connectivity facilitates an easy and highly productive workspace whereby the improved information flow accelerates a positive change in organizational synergy, operational efficiency and profitability. We provide solutions from the plant floor to the top floor with a fully integrated enterprise document and data management solution; creating an agile business environment. eInfotree enables your organization to capture, process and manage information more efficiently. This reduces costs, improves service levels and decreases project and customer response time, while providing an excellent return on investment. The browser-based application is complemented by a number of modules that add value in key application areas.

Revolutionize your Life Sciences processes. Drastically improve the control, efficiency, and quality of your processes and products. Ensure inspection readiness at all times through our fully compliant platform, pre-validated according to GAMP5. Maintain total control over processes and documents, customize workflows to perfection, and automate where possible. Enjoy uninterrupted workflows and full traceability through seamlessly connected and integrated modules. Our dedicated team is ready to answer your questions at any time. Only a first-class Scilife experience will do! Our Scilife platform streamlines automates and organizes every process in your industry space, whether you’re in Medical Devices, Pharma & Biotech, or ATMP. Click below to discover which Scilife modules support your unique industry lifecycle stages. Our software is equipped with all the advanced quality tools you would expect, and a bunch more that go above and beyond!

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.

The AssurX platform is a versatile enterprise quality management system (EQMS) and regulatory compliance management platform. AssurX allows enterprises of any size or complexity to create a system that reliably communicates and coordinates quality and compliance information, documentation, and activities across the enterprise. AssurX allows regulated businesses to quickly identify and control risk exposure and avoid quality or noncompliance problems while improving workflow. AssurX QMS software is highly configurable to fit any established or dynamic business requirements. The system creates an electronic workflow of tasks, alerts, escalations, and approvals that can be automated to the desired level, mapping precisely to real-world operations. Begin with just the solutions and functionality you need now, then implement what you like whenever you’re ready. No other system is easier to deploy, configure, and modify.

Quality, Safety and Environmental Management Systems can seem complex and hard to maintain. But we're here to help - we know the standards back to front, and have built Toolbox to help you get your systems humming, get compliant and improve your business along the way. We strongly believe that when done right, QHSE management systems are not difficult and hard to maintain - and because the requirements are based on sound business fundamentals, your business improves too. It's a system and a workflow to organize, manage, share, and track an organization’s files and documents. Controlling your documents results in savings in time, effort and frustration, reduced business continuity risk. Toolkit includes a workflow that allows a document to contain both an in-development version, and a released version for general perusal. We also store superseded versions and track all changes in an detailed audit log. Team members can subscribe to kept up to date with all changes.

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.

NiftyISO 9001 Audit software streamlines quality management, ensuring compliance, efficiency, and consistency across your organization. Accessible on the web, mobile, and tablets, it empowers you to improve quality from anywhere, enhancing operations whether in-office or remote.

SoftExpert EQM is the most comprehensive enterprise quality management software (EQMS). It helps companies to achieve and maintain ISO 9001 certification through automated, highly interactive quality processes tailored to an organization’s specific products, operations and business practices. As a modular and scalable solution platform, SoftExpert Quality Management Software seamlessly integrates all key quality initiatives, including process mapping, documented information (SOP – standard operating procedures, work instructions and records), non-conformance reports (NCR/NCMR), corrective/preventive actions (CAPA), quality indicators (KPIs). The solution also manages supplier relations, customer complaints, quality audits, competence and training, quality risks and controls, quality inspection and statistical process control, increasing QMS agility and robustness.

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.

Automate the identification, containment, investigation, and resolution of problems within your organization and supply chain. Trusted by thousands of users globally, this is one of the best CAPA software applications available. CAPA Manager corrective action software automates the assignment, notification, investigation, reporting, and approval of corrective actions. It error-proofs the control of the entire CAPA process, from initiation to investigation and all the way through to closure. CAPA Manager meets the requirements of all important quality management standards: 21 CFR part 11, ISO 9001, AS9100, TS 16949, and more. It keeps records of root-cause and corrective action while providing pre-defined workflows and approval gates.

Focus BIS provides a range of extensive cloud-based management systems to meet the requirements of quality, safety and the environment. Based on the framework requirements of International Standards 9001, 45001 and 14001- so you get great value. Focusbis specializes in Integrated Management Systems (IMS) – usually this means ISO9001 Quality Management Systems, ISO45001 Occupational Health and Safety Management Systems and ISO14001 Environmental Management Systems. In addition to this FocusBIS also has experience in industry-specialized accreditation schemes such as the Accreditted Service Provider Level 1 scheme for electrical organizations providing distribution network electrical services and mining and quarry operations. Many organizations are experiencing increased regulatory requirements, especially when pursuing diversification. Integration of operational and management systems is often key to effectively and efficiently managing accreditation and regulatory requirements.

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.

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.

IMSXpress is a cutting-edge document control and quality management system (QMS) software solution. Easy to install and intuitive, IMSXpress Quality Management improve the overall business efficiency while maintaining compliance. The solution offers a plethora of modules, such as document distribution, document control, internal audit, training, management review, Corrective/Preventive Action (CAPA), customer companies, risk management, preventative maintenance, measuring equipment, supplier control, and more.

Ensure quality and GxP compliance with Vault QMS. With built-in best practices and automated workflows, Vault QMS brings all parties – pharma and biotech companies, contract manufacturers, and suppliers – into quality processes for better control and visibility. Easily bring departments, sites, suppliers, contract manufacturers, contract test labs, and other partners into continuous quality improvement processes. Increase operational efficiency with automated workflows and built-in best practices. Improve risk visibility across products and processes with a unified approach to risk management. Improve speed, efficiency, and GxP compliance with a unified suite of quality applications. Readily enable quality management processes with built-in best practices for deviation, internal and external audits, complaints, lab investigations, change control, CAPA, and quality risk management.

Ennov Quality Suite. A comprehensive QMS to improve efficiency and ensure compliance. Ennov Quality Suite Ennov’s Quality suite combines the power and flexibility of Ennov Doc, Ennov QMS, Ennov Report and Ennov Training to create a quality management solution that not only improves operational efficiency but also ensures compliance with industry standards such as 21 CFR Part 11, GxP and ISO. Ennov Quality provides a predefined inventory of quality documentation, processes and workflows that are based on accepted industry standards and best demonstrated practices. This allows Ennov Quality customers to get their system into production quickly and start realizing their return on investment. Ennov Quality, like all Ennov solutions is very easy to configure and requires no IT skills. An intuitive and unified content and information management platform to support and enrich the entire Life Sciences product life cycle. Our comprehensive QMS improves operational efficiency

AuditComply is a Belfast-headquartered Enterprise Risk Management Platform. Developing & providing comprehensive solutions for Risk, Quality, Compliance & EHS. A SaaS-based solution to spot hazards/issues, monitor risk, tackle uncertainty and boost performance. The company operates in highly regulated industries such as Automotive, Food & Beverage, Oil & Gas, Aviation and Manufacturing. With key clients situated throughout the UK, EU, US, Middle East and Asia Pacific regions. AuditComply has combined the comprehensive enterprise workflow with the speed and ability to deploy a mobile-first app. Enterprise customers select us because we deliver value on day one. We embrace change seamlessly to meet their daily needs, promote visibility, reduce costs and drive operational efficiencies whilst anticipating and managing enterprise risk. Deliver engaging reports with dynamic risk scoring, summaries, control matrices & more.

CWA SmartProcess is a robust business process management (BPM) software Software for workflow management, process management, and quality management. This web-based solution enables simple modeling, optimization, and publication of processes and documents using a single platform. CWA SmartProcess provides optional modules for measures, tasks, claims, complaints, and audits. With CWA Smart Process, you can seamlessly automate processes as workflows and achieve continuous improvements in your business.

Quality Inspector by Insight Works is a comprehensive quality control app. It empowers companies to enhance product quality, reduce costs, and maintain compliance. It integrates seamlessly with Microsoft Dynamics 365 Business Central with customizable entry forms and various inspection types. Quality Inspector simplifies data collection and automates processes. It offers real-time visibility into quality issues. Benefits * Streamlined Inspection Processes * Enhanced Quality Control * Improved Data Management * Increased Compliance and Process Control * Better Decision Making and Reporting Features * Inspection Execution: Benefit from a mobile-friendly user interface, automated test creation, and support for various test result types. * Data Management & Integration: Centralize inspection data, store detailed test information, and add supporting documents. * Process Control & Compliance: Utilize retest features, and enforce inspections before specific activities.

The fact that all versions of a document or registration folder are separated out into different modules depending on their state (draft, approved, valid and historic) in the lifecycle gives a unique overview of the document management system. Creating registration forms (using the built-in HTML editor), registration fields and registration workflows are very easy and at the same time registrations in Visual Quality are much more feature rich that what our competitors have to offer. All registrations are processed (created or approved/rejected) in Visual Quality Web Access. Thanks to the great Visual Quality community who help shaping the product, Visual Quality is evolving quickly. Our development schedule is very aggressive and we are committed to equip you with the leading software for building and maintaining your quality management system.

ZipQuality is a software-enabled service that assists medical device companies in bringing new products to market. Our collaboration platform manages rapid design changes for agile teams while ensuring regulatory compliance. Pre-configured system(processes and tools); no need to alter your quality system. The integrated system easily handles rapid design iterations for product documentation. Experienced consultants guide your team at every step. Fully-featured, scalable software tools built on the proven, powerful ENOVIA platform. Our integrated system enables rapid design changes while keeping product documentation and data in sync and maintaining all the records in an audit-ready state. Product requirements, hardware requirements, software requirements. We understand complex, software-intensive medical devices. The ZipQuality system is based on a structured documentation framework that supports good systems engineering, efficient risk management, and clear traceability.

Document Control is a document management service whose purpose is to support controlled processes and practices for creating, reviewing, correcting, issuance, and distributing of documents. ISO standard-based QMS QISS Offers CAPA Management Software System for Automating Corrective Action Processes in Regulatory Environments. Adopt your own risk-based thinking. Centralize to prevent and mitigate your risks. Standardized workflow helps you stay in control of changes in your organization. Build a paperless document management system with numerous additional benefits. Develop a culture of continuous improvement with the visibility of each non-conformance.

Let camLine create with LineWorks MES a powerful Manufacturing Execution System (MES) which is perfectly tailored to the individual needs of your production. With the flexibly combinable modules of the LineWorks Suite, the most essential functionalities are already available. The path to an MES tailored to your needs is based on established and continuously improved software products that have been in use for many years. Individual requirements can be flexibly supplemented in the form of use cases. They reflect the best practices for increasing efficiency, quality, and reliability that have been repeatedly optimized over many years as they have established themselves over the last decades in the sense of a cultural footprint in manufacturing. You get an agile solution that can be constantly adapted to the future requirements of your production. You decide on an infrastructure solution whose components have proven themselves on the market for many years due to their high robustness.

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.

Companies use TIPQA to achieve continuous and measurable improvements while advancing customer service, productivity and profitability. Our QMS software allows industry leaders to control compliance and effectively manage quality within their supply chain. TIPQA QMS Software supports best practices in quality and will help you build a comprehensive continuous improvement strategy for your organization. Use of the TIPQA quality management solution has resulted in proven, documented success by countless companies that demand delivery of highly regulated, quality products. TIP Technologies has more expertise in understanding complex quality business processes in a regulated manufacturing environment than any other solution pro­vider. The TIPQA quality management solution allows its users to remain agile, allowing them to adapt to ever-changing markets and quality requirements. TIP Technologies continuously develops its quality management system.