Alternatives to Qualios

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

Founded in 2004, Sunday Business Systems (SBS) specializes in providing quality management software and consulting services that help businesses comply with a range of ISO certifications like ISO 9001:2015 and ISO 13485. SBS’s product suite includes tools for document control, asset tracking, corrective actions, and preventive maintenance. Their cloud-based solutions are designed to simplify and automate key business processes, while their consulting services offer expert guidance for businesses aiming for ISO certification or requiring customized software for manufacturing or compliance needs.

QRA’s tools streamline engineering artifact generation, evaluation, and prediction, refocusing engineers from tedious work to critical path development. Our solutions automate the creation of risk-free project artifacts for high-stakes engineering. Engineers often spend excessive time on the mundane task of refining requirements, with quality metrics varying across industries. QVscribe, QRA's flagship product, streamlines this by automatically consolidating these metrics and applying them to your documentation, identifying risks, errors, and ambiguities. This efficiency allows engineers to focus on more complex challenges. To further simplify requirement authoring, QRA introduced a pioneering five-point scoring system that instills confidence in engineers. A perfect score confirms accurate structure and phrasing, while lower scores prompt corrective guidance. This feature not only refines current requirements but also reduces common errors and enhances authoring skills over time.

ARMATURE Fabric™ provides a comprehensive solution for overseeing your accreditation, certification, credentialing, audit, quality, and compliance processes all within one cohesive platform. By utilizing our software, you can enhance efficiency, improve security, and deliver superior service to your stakeholder communities. No matter if you are working with institutional, programmatic, or specialized accreditation programs, certifying various individuals or organizations, conducting thorough audits, or addressing non-conformances, ARMATURE Fabric streamlines these activities for both you and your stakeholders, ensuring a more productive experience. Our cloud-based software ensures data collection through a variety of methods, including online applications, assessments, audits, inspections, surveys, and self-evaluations. Additionally, it allows you to handle workflows related to accreditation, certification, audits, and compliance while efficiently managing documents and identifying issues. With features that enable reporting and trend analysis, ARMATURE Fabric empowers organizations to proactively adapt and improve their practices.

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

All-in-One LIMS, ELN, QMS, and DMS Platform Xybion LIMS is an all-inclusive Digital Laboratory system including LIMS, ELN, QMS, and DMS that creates optimized workflows for the unique business needs of all regulated laboratories including research, diagnostics, quality control, stability studies, and more. Xybion LIMS 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.

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. This technology ensures that everyone can work as efficiently and effectively as possible. You won't miss any issues. Qooling allows each member of your team to easily create a report on nonconformity by simply taking a photo with their smartphone. You can stop worrying about outdated procedures and work-instructions. Qooling takes care of all aspects of version control, making sure that everyone has the correct version. Qooling has many cool features.

Intellect's QMS software has been proven to improve quality operations and reduce overall quality cost by up to 40%. Our apps were designed by certified quality professionals and can be easily customized with our no-code platform or drag-and-drop technology. Remote access for your team, mobile apps, dynamic workflows, analytics, reporting, and remote access are all possible with this modern and simple solution. Apps include Document Control and Employee Training, Audit Management CAPA, Nonconformance, as well as other useful features.

Qualtrax is a quality and compliance software program that can manage and control documentation, automate key business processes, streamline training management, manage external and internal audits, and ensure that critical industry regulations are met in real time. Qualtrax is a valuable resource in highly-regulated industries where compliance with standards such as ISO 17025 and 17020, 13485 and 9001, TNI and GFSI, FDA and FQS are required.

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.

Qualio is a one-stop solution for quality and compliance management. It's ideal for growing companies in healthcare and life sciences. Qualio is reliable, affordable and easy to use. It helps companies build life-saving products faster and achieve 100% ISO, GxP and FDA compliance. Qualio makes it easy for companies to manage document control, training and NCRs, audits as well as suppliers, complaints, and other tasks in one platform.

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

QSE SMART is a specialized software application for quality, safety, environmental, and risk management, tailored for small to mid-sized businesses and projects accommodating between 5 to 500 users. This application offers a robust framework that aligns with essential ISO standards such as ISO9001, ISO45001, and ISO14001, thereby streamlining the daily operations of your integrated QSE management system. By making ISO standards relevant to your business, QSE SMART enhances understanding and implementation. Built on a risk-based methodology in line with ISO 31000, it empowers organizations to gather and utilize critical data and metrics that align with their goals regarding quality, safety, environment, and risk management. This includes tracking objectives and targets, conducting management reviews, identifying risks and opportunities, managing non-conformities and improvements, performing audits and inspections, and addressing accidents, incidents, and hazards. Additionally, it covers corrective actions, equipment calibration, and the control of documented information, ensuring comprehensive oversight and continuous improvement in your organization's processes.

With a platform which puts you on cruise control, you can drive exceptional quality and process performances. E-Data Now® Audit & Quality Inspection Platform is a powerful tool that allows you to improve customer satisfaction, reduce safety concerns, and eliminate redundant processes. It includes all the tools needed to connect team performance, simplify checks, identify root causes of non-conformance and improve processes. E-Data Now! E-Data Now! is a cloud-based, no-code platform that provides insights into mobile data and automates workflows. Clearing out your paperwork will help you to reduce the amount of clutter in your audit process and identify any audit redundancies. The simple solution - a platform for creating custom forms and mobile data collection with digital tools designed for tradesmen: to train, record and capture, react, correct and schedule, comply, and build better processes.

TRACKMEDIUM is a cloud-based Quality Management System (QMS) software tailored for small to medium enterprises (SMEs), operating on a subscription model that offers a variety of modules such as Audit Management, CAPA, Document Control, Management of Change, Nonconformance Management (NCM), and Training Management. This platform empowers organizations to enhance product quality and safety, boost operational efficiency, and ensure adherence to industry regulations like ISO 9001, 14001, and OSHA, all while minimizing costs and mitigating risks. The Audit Management module of TRACKMEDIUM simplifies the audit process by allowing users to create standardized templates for audits and checklists, formulate comprehensive audit plans, carry out audits, pinpoint nonconformances and recommendations, manage CAPAs until resolution, and effectively report on findings. Additionally, TRACKMEDIUM's user-friendly interface and comprehensive support make it an ideal choice for businesses looking to integrate quality management seamlessly into their operations.

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.

The Plex Quality Management System (QMS) enables both process and discrete manufacturers to adhere to stringent industry standards and customer requirements through an integrated digital record-keeping system. By facilitating consistent and reliable quality assurance via in-line quality measures, transparent reporting, and straightforward audit tracking, it ensures that manufacturers can maintain compliance effortlessly. With real-time access to quality documentation available digitally throughout the organization, businesses can effectively meet regulatory demands while fostering operational efficiency. Enhanced delivery performance, improved supplier relationships, and greater customer satisfaction contribute to sustained growth in both new and repeat business. By embedding quality management into everyday workflows and processes, the risk of quality-related losses, warranty claims, or product recalls is significantly minimized, ultimately enhancing brand image and customer loyalty. Furthermore, Plex enables the creation of detailed process control plans that include specific inspection protocols and digital checklists, streamlining quality oversight across various operational areas. This comprehensive approach to quality management not only safeguards compliance but also drives continuous improvement and innovation within the manufacturing sector.

myQualityTM serves as an online portal for ISO 9001 quality management systems tailored for both quality professionals and consultants. It offers a thorough collection of necessary documented information that is ready for assessment, design, implementation, certification, and continuous support. Gaining a basic understanding of the platform is straightforward, but fully leveraging its robust capabilities will require additional time and will be integral to your ongoing improvement efforts. Merely purchasing the software and completing the training is akin to acquiring a computer solely for web browsing; true value emerges when you learn to optimize it as a genuine investment. Fortunately, we offer an extensive range of 'How To' resources alongside our Tech Support to assist with all other inquiries. The platform is equipped with the essential documented information requirements through user-friendly, interconnected databases, registers, templates, forms, procedures, and a plethora of other resources. A one-time setup fee grants you a dedicated company domain, five managerial accounts, and unlimited user access, ensuring your team can fully engage with the system. This setup not only streamlines your quality management processes but also positions your organization for sustained growth and compliance in the future.

Starting now, you can effortlessly obtain all the essential documents without sacrificing your valuable work hours and at an attractive price! The subscription process is straightforward; just a few clicks will bring you to the purchase screen. There, you can input your company’s details, including the organization name, logo, and information regarding the procedures approver. Simply complete the forms and implement them according to the ISO 9001 standards presented on your screen. You can easily access controlled reports and forms featuring your organization's name and logo, ensuring you’re well-prepared for the external audit. You can also handle the preparation on your own time, eliminating the need for external assistance. The system is available all year round, allowing you to enter data whenever it suits you. Don’t leave things to the last minute! Everything you need for a robust quality management system is included, along with the ability to create controlled forms emblazoned with your company logo. This all-in-one solution ensures you have everything necessary for the external audit and your ISO quality management system conveniently at your fingertips. By streamlining the process, you can focus on what truly matters—growing your business.

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

Quarta EVO is an online Quality Management software designed for Quality Assurance and Compliance, leveraging a robust workflow engine. This platform enables the digitization of quality systems and allows users to monitor processes seamlessly from any location, utilizing an integrated internal dashboard and key performance indicators (KPIs). It serves as an effective QMS solution to enhance and oversee the performance of Quality and Safety Management Systems within organizations. Built on a powerful workflow engine, it merges extensive functionality with modern web-based architectures and technologies, all aimed at facilitating collaboration across different plants and evaluating process performance. The Quarta suite stands out for its user-friendly, fluid, and intuitive interface, capable of gathering real-time data, performing analysis, organizing information, and automatically generating a series of indicators to maintain comprehensive oversight of the entire Quality System. As a result, organizations can expect improved efficiency and enhanced compliance through the use of this innovative software solution.

Trevally from ManualMaster is a comprehensive QHSE platform designed to cover the entire PDCA loop in a single web or on-premises solution. It provides controlled document and version management with audit trails, process mapping, risk and standard controls, as well as quality assurance registrations and smart web forms. Additional modules manage incidents, complaints, audits, deviations, tasks, and actions, all displayed in role-based dashboards with real-time KPIs, reports, and graphs. With ISO-27001 hosting, backups, single sign-on, two-factor authentication, and granular user permissions, Trevally ensures data security while supporting multi-language interfaces, digital signatures, and mobile access for enhanced user adoption.

Crafted and verified by our team of SPC and Six Sigma experts, this software stands out as one of the most adaptable and cost-effective solutions for the analysis of statistical process control (SPC) data. Additionally, it is capable of calculating six sigma process metrics and forecasting the process average for Engineering Process Control (EPC). This tool is essential for organizations and students aiming to excel in Six Sigma methodologies. Our management consultants bring extensive experience in the successful implementation of a range of management systems including ISO9001:2015, ISO14001:2015, ISO17025:2017, ISO22000:2018, ISO27001:2013, ISO45001:2018, ISO50001:2018, and SA8000:2014 across various client organizations globally. Drawing from their extensive background, our consultants have developed comprehensive, step-by-step guidelines for system implementation, offering precise instructions for managers and representatives tasked with planning and executing these systems. Adhering to these guidelines can significantly reduce both the cost and timeline of your projects, making processes more efficient and effective. Organizations that leverage this software alongside our experts’ insights can enhance their operational excellence.

Managing Quality, Safety, and Environmental Management Systems may appear daunting and challenging to sustain. However, we are here to assist you, as we possess an in-depth understanding of the standards and have developed Toolbox to streamline your systems, ensure compliance, and enhance your business performance in the process. We firmly maintain that with the right approach, QHSE management systems can be straightforward and manageable; since they are grounded in robust business principles, implementing them leads to overall business improvement as well. This system serves as an organized workflow to manage, share, and oversee an organization’s files and documents effectively. By controlling your documents, you can save time, reduce effort and frustration, and minimize the risk to business continuity. The Toolkit features a workflow that accommodates both a version of a document that is still in development and a finalized version available for public access. Additionally, it retains previous versions and maintains a comprehensive audit log to track all changes. Team members have the ability to subscribe for updates, ensuring they stay informed about all modifications. Furthermore, this proactive approach not only simplifies document management but also fosters collaboration and transparency within the organization.

The AssurX platform is a powerful software platform for enterprise quality management (EQMS) and regulatory compliance to reliably communicate and coordinate information, documentation, and activities. AssurX allows regulated businesses to quickly identify and control quality issues and risk exposure to avoid quality or noncompliance problems while improving workflow. AssurX QMS software is uniquely 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. No other system is easier to deploy, configure, and modify. AssurX solutions integrate seamlessly to create a connected quality system. Solutions include audit management, corrective actions, training management, compliant management, document management, change control, risk management, EHS incident management, and more.

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

SoftExpert EQM stands out as an all-encompassing enterprise quality management software (EQMS) that aids organizations in obtaining and upholding ISO 9001 certification by automating and enhancing quality processes specifically designed for their unique products, operations, and business practices. This modular and adaptable platform integrates all essential quality initiatives, including process mapping and the management of documented information such as standard operating procedures, work instructions, and records, along with non-conformance reports, corrective and preventive actions, and quality indicators. Furthermore, the software efficiently oversees supplier relationships, addresses customer complaints, conducts quality audits, manages training and competencies, and evaluates quality risks and controls, as well as quality inspections and statistical process control, all of which contribute to a more agile and resilient quality management system. By streamlining these diverse functions, SoftExpert EQM empowers organizations to enhance their overall quality performance and compliance.

QwizPRO revolutionizes quality management for compliance with ISO 9001 and AS9100, making audits effortless and efficient. By utilizing its intuitive automation, the platform reduces errors, conserves time, and enhances the compliance journey. In the fiercely competitive landscape of modern business, QwizPRO is crucial for achieving quality excellence without complications. It enables consistent monitoring and assessment of suppliers, ensuring they meet your rigorous quality standards. Featuring real-time analytics and customizable reporting options, the software provides insightful visibility into supplier performance, showcasing strengths while pinpointing potential vulnerabilities. Equip your team with tailored QMS training that progresses from a basic grasp of industry standards to a comprehensive understanding of intricate procedures. QwizPRO facilitates automatic training deployment, tracks learning advancements, and uncovers areas needing improvement. Additionally, the software ensures immediate access to essential documents necessary for daily operations, further optimizing productivity and efficiency. With such capabilities, QwizPRO stands out as an indispensable tool for organizations striving for continuous quality enhancement.

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.

Enhance your quality management by simplifying workflows, consolidating data, maintaining compliance, and attaining operational excellence through our comprehensive QMS solution. With user-friendly graphical dashboards, you can gain real-time insights that empower informed decision-making and enable effortless performance tracking. Our QMS platform supports efficient data gathering, continuous monitoring, and insightful analysis to promote proactive quality management. It allows you to easily identify trends, encourage collaboration, and ensure compliance, thus optimizing your processes with minimal effort. Furthermore, our quality management platform is equipped with unique features tailored to refine and elevate your quality management practices, ensuring more efficient operations and improved outcomes. By leveraging this solution, you position your organization for sustained success and growth in a competitive landscape.

Automate the identification and resolution of problems in your organization and supply chain. This is one of the most trusted CAPA software applications. It has been trusted by thousands of users worldwide. CAPA Manager corrective actions software automates the assignment of corrective actions, notification, investigation and reporting. It prevents errors in the control of the entire CAPA process from initiation through investigation and closure. CAPA Manager meets all requirements of the most important quality management standards, including ISO 9001, AS9100 and TS 16949. It maintains records of root-cause and corrective actions, and provides pre-defined workflows with approval gates.

Insight Works' Quality Inspector is a comprehensive app for quality control. It allows companies to improve product quality, reduce costs and maintain compliance. It integrates seamlessly into Microsoft Dynamics 365 Business Central, with customizable entry forms and different inspection types. Quality Inspector automates and simplifies processes. It provides real-time visibility of quality issues. Benefits • Streamlined inspection processes • Quality Control Enhanced • Improved Data Management • Improved compliance and process control • Better Decision Making & Reporting The following are some examples of • Inspection Execution : Take advantage of a mobile-friendly interface, automated test creation and support for different test result types. • Data Management and Integration: Centralize inspection information, store detailed test data, and add supporting documentation. • Process Control & Compliance : Use retest features and enforce inspections prior to specific activities.

Virje meets the standards set forth by 21 CFR Part 11, 21 CFR Part 820, and ISO 13485. If you're feeling daunted by the complexities of Part 11 software validation, rest assured that help is just a click away, no matter where you are or when you need it. By eliminating paperwork, cutting costs, and enhancing productivity through automation and unified collaboration, it becomes an ideal solution for small to medium-sized enterprises. Designed specifically for medical device quality management, this system is constructed to be adaptable to your unique workflows and processes, ensuring you don’t have to make any sacrifices. It features configurable change order approvals that can be tailored by employee role and document type, along with timely notifications sent to accountable team members throughout every phase of the change process. Users can assign material dispositions for specific documents, gain easy access to both released and archived versions, and quickly view the history of document changes. Additionally, it tracks where-used locations and the distribution of hard copies, while also providing reminders for periodic document reviews to ensure compliance and efficiency remain top priorities. This comprehensive approach not only streamlines quality management but also empowers organizations to maintain rigorous standards effortlessly.

The division of all document versions or registration folders into distinct modules based on their status (such as draft, approved, valid, and historic) throughout their lifecycle provides a distinctive perspective on the document management system. The process of creating registration forms with the integrated HTML editor, along with registration fields and workflows, is straightforward; additionally, the registration capabilities in Visual Quality are significantly more advanced than those offered by our competitors. Registrations are handled—whether created or approved/rejected—through Visual Quality Web Access. With the support of the vibrant Visual Quality community contributing to the product's development, Visual Quality is rapidly progressing. Our development timeline is notably ambitious, and we are dedicated to providing you with top-tier software to establish and uphold your quality management system. This commitment to innovation ensures that our users always have access to the latest features and improvements in the industry.

QUALIPRO is a comprehensive management software designed for quality, environmental, occupational health and safety, and food safety management. It offers assistance, research, and consulting services in quality, environmental issues, workplace health and safety, and HACCP standards. The software also provides training and awareness programs related to quality, environment, health and safety at work, food safety, and auditing techniques. Its customizable nature and specialized modules allow QUALIPRO to meet the specific needs of the Pharmaceutical and medical device industries effectively. QUALIPRO adheres to the principles of “Good Manufacturing Practices (GMP)” and complies with ISO13485 standards. Additionally, it aligns with key international standards such as ISO 9001, EN 9100, ISO IATF 16949, ISO 14001, ISO 17025, ISO 15189, ISO 22000, IFS, ISO 27001, and ISO 45001. As a state-of-the-art and modular software solution, QUALIPRO serves as a powerful tool for managing Quality, QSE, SHEQ, and SHE systems. Its versatility makes it an essential resource for organizations striving for excellence in quality and safety management.

Document Control is a document management system that supports controlled processes and practices in creating, reviewing, correcting and issuing documents. The QMS QISS is an ISO-based QMS QISS Software System that automates corrective action processes in regulatory environments. Your own risk-based thinking. To reduce and mitigate your risk, centralize. Standardized workflows allow you to keep track of all changes within your organization. You will enjoy many additional benefits from a paperless document management system. Establish a culture of continuous improvement and make sure that each non-conformance is visible.

CWA SmartProcess is a comprehensive software solution designed for effective business process management (BPM), focusing on workflow, process, and quality management. This online platform allows users to easily model, enhance, and share processes and documents from one centralized location. Additionally, CWA SmartProcess offers optional modules that cater to various needs, including measures, tasks, claims, complaints, and audits. By utilizing CWA SmartProcess, businesses can effortlessly convert their processes into automated workflows, fostering ongoing improvements and efficiency within their operations. Ultimately, this tool empowers organizations to streamline their processes and enhance overall productivity.

Transform your Life Sciences operations by significantly enhancing the control, efficiency, and quality of your products and processes. Maintain inspection readiness consistently with our fully compliant platform, which has undergone pre-validation in line with GAMP5 standards. Gain complete oversight of your processes and documentation, allowing for perfectly customized workflows and maximized automation wherever feasible. Experience smooth operations and comprehensive traceability through our seamlessly connected modules. Our committed team is available to address any inquiries you may have at any moment. Only the finest Scilife experience meets our high standards! The Scilife platform not only streamlines but also automates and organizes every aspect of your industry, whether in Medical Devices, Pharma & Biotech, or ATMP. Click below to explore the specific Scilife modules that cater to the distinct lifecycle stages within your industry. Our software is not just equipped with all the essential quality tools you would anticipate; it also comes with numerous additional features that surpass expectations, ensuring your operations thrive. We're excited to partner with you on this transformative journey!

OpenText ALM Quality Center is a single-pane-of-glass for software quality management. It helps you implement rigorous and auditable lifecycle process and govern application lifecycle activities. Use the reusability and traceability of ALM tools, as well as their automation, to improve efficiency when developing, testing and maintaining applications. Automate the collection of results and gain real-time insight into application quality by eliminating time-consuming, error-prone manual processes. Standardize processes with templates and workflows built into ALM. Ensure compliance through detailed change tracking, a risk-based strategy and detailed change tracking. Integrate and use APIs to create a vendor-neutral, automated ecosystem for data consolidation throughout your application lifecycle. Choose the deployment option that best meets your needs for scalability and security.

Organizations utilize TIPQA to foster ongoing and quantifiable enhancements while enhancing customer service, productivity, and profitability. Our Quality Management System (QMS) software empowers industry leaders to maintain compliance and manage quality efficiently within their supply chain. The TIPQA QMS Software champions best practices in quality management and aids in crafting a thorough continuous improvement strategy tailored for your organization. The implementation of the TIPQA quality management solution has led to tangible, documented successes for numerous companies that prioritize the delivery of highly regulated and quality-assured products. TIP Technologies has unparalleled expertise in navigating intricate quality business processes within regulated manufacturing environments when compared to any other solution provider. With the TIPQA quality management solution, users can stay agile, adapting seamlessly to fluctuating market dynamics and evolving quality standards. Additionally, TIP Technologies is committed to the ongoing enhancement of its quality management system, ensuring it evolves to meet the demands of its users. This dedication positions TIPQA as a forward-thinking solution in the realm of quality management.

Paradigm 3 is a comprehensive platform available for both web and desktop use, tailored to assist businesses with compliance management focusing on Document Control, CAPA Compliance, and Competency Tracking and Training. This software provides a variety of features, including an event manager for handling incident investigations and customer complaints, email-delivered task notifications, and tools for preparing audits, among others. Industries such as Healthcare, Manufacturing, Test Labs, and Service Industries greatly benefit from the functionalities of Paradigm 3. With this innovative solution, organizations can eliminate the need for multiple additional modules to fulfill their compliance requirements. The system consists of four primary modules equipped with over 50 standard forms designed to address all aspects of Quality, Safety, and Environmental management. Furthermore, our form designer empowers users to create customized forms or modify existing ones, ensuring that every specific need is met seamlessly. This flexibility in form design enhances the platform's utility, making it an indispensable tool for businesses striving for compliance excellence.

The eInfotree™ Quality Management System offers a cohesive strategy for Enterprise Information Management by seamlessly integrating data and business workflows in an intuitive way. This integration fosters an efficient and productive work environment where enhanced information flow promotes positive developments in organizational synergy, operational effectiveness, and overall profitability. Our solutions cater to all levels of the organization, from the factory floor to executive management, providing a comprehensive system for enterprise document and data management that fosters business agility. By leveraging eInfotree, your organization can more effectively capture, process, and oversee information, resulting in reduced costs, heightened service quality, and quicker project and customer response times, all while ensuring a strong return on investment. The browser-based platform is further enhanced by various modules designed to add value in critical application areas, supporting continuous improvement across the organization. Ultimately, eInfotree empowers companies to adapt swiftly to changing market demands while maintaining high standards of operational excellence.

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.

InstantGMP™, which replaces multiple software and/or paper-based solutions for managing your manufacturing and compliance needs, could be the key to unlocking your business's full potential. With a single, affordable software solution, you can easily increase production uptime, improve batch quality, and meet all FDA compliance requirements. InstantGMP™, which can be used individually or together depending on your business needs, delivers comprehensive, integrated software solutions that ensure quality, consistency, and GMP compliance. We will help you choose the right solution for your business today and tomorrow. You can organize, manage, and document batches electronically while promoting good manufacturing practices. Inventory Management Software that meets Part 11 requirements and GMP requirements. A complete quality system with templates, SOPs and guided workflows that is ideal for virtual biotech.

Workflows are specifically developed to assist you in preparing all necessary components for a 510(k) submission, while also ensuring compliance with the quality record requirements set forth in 21 CFR Part 820 as you prepare to market your device. These workflows come equipped with tools to facilitate the drafting of essential policies, procedures, and work instructions. Furthermore, you can monitor non-conformances, deviations, and CAPAs through tailored quality management reports. As your processes evolve and enhance, you can ensure your team receives automatic training updates. The system also automates validation testing for devices, applications, websites, and custom software tailored to your business needs. This automation significantly reduces the time and resources that would otherwise be consumed by extensive testing, reporting, and approval processes. Additionally, you can compile all your policies, procedures, and artifacts into standard documents, making them readily available for audit evaluations. Overall, this solution streamlines the compliance and validation processes, thereby enhancing operational efficiency.