Alternatives to SBS Quality Database

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

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

It is difficult to make data available and actionable when a manufacturing site has many processes. As operations grow, it is becoming more difficult to comply with safety, quality, and environmental regulations. Manufacturing is built on predictability and reliability. Manufacturing by nature is all in the execution of established processes. TenForce was built from the feedback of our clients to map the operational reality in a plant.

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

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.

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.

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

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

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

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

Unify quality processes with QT9's all-in-one cloud-based QMS Software Suite. QT9 QMS is a user-friendly quality management software that includes 25+ modules with unlimited scalability. Automate ISO & FDA Compliance with email alerts, To Do lists and FDA 21 CFR Part 11 Compliant Electronic Approvals. QT9 QMS enables Life Sciences, Biotechnology Companies, Medical Device Manufacturers and Pharmaceutical Companies to digitally transform operations. Get real-time status updates and visualize quality metrics up-to-the-minute. QT9 QMS comes with built-in document control, revision-level controls, corrective actions (CAPAs), Nonconforming products and more. Advance product releases with Deviation Management, Engineering Change Orders, FMEA, Inspection Management Modules Included. Go paperless & put time-consuming tasks on autopilot. QT9 QMS comes ready-to-use. Get a free product tour! Start a Free Trial. Visit QT9qms.com

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

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

Quality Planning Studio's FMEA software combines essential quality tools while guaranteeing compliance with key process flow stages. This all-in-one software solution facilitates the planning, documentation, and oversight of vital quality standards. For manufacturers around the globe, FMEA has become a crucial element of ongoing improvement initiatives. The interconnectedness of Process Flows, FMEA, control plans, and SPC is pivotal to fostering quality enhancement. Through the FMEA process, there is a continuous drive to refine products, processes, or detection methods. Engineers engaged in the FMEA process receive ongoing insights from SPC outcomes observed on the shop floor. The QPS database effectively centralizes all information, maintaining the traceability and integrity of your Process Flow, FMEA, and Control Plan data across various manufacturing locations. Additionally, QPS can integrate with our SPC software, DataMetrics, which streamlines operations by minimizing redundancy while enabling effective monitoring of characteristic capabilities derived from the Control Plan. This seamless integration ultimately enhances overall operational efficiency and quality assurance.

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.

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

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.

The Audit Manager software facilitates comprehensive quality management by enabling the digital oversight of audits, quality controls, and testing throughout all stages, including planning, checklist creation, evidence collection, field surveys, and the management of nonconformities. Users can easily access the calendar to schedule audits while attaching essential details such as the subject, checklist, lead auditor, co-auditor, and participants. Both internal and external personnel can receive timely email invitations and view the audit schedule directly through the application. After completing the inspection, users can generate audit reports in PDF or Excel formats and share them instantly with company management or relevant stakeholders via mobile. All minutes are neatly archived and accessible, ensuring that they can be seamlessly integrated into the document repositories utilized by the organization, enhancing overall efficiency and accountability in the audit process. This streamlined approach not only saves time but also improves communication among all parties involved.

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

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!

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

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.

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

SoftExpert FMEA is a comprehensive software solution designed for organizations to effectively oversee Failure Modes and Effects Analysis. By adopting a proactive stance, it allows businesses to forecast potential defects, thereby ensuring the quality of their outputs. This methodology can be utilized across various domains, including products, processes, departments, and assets, leading to a reduction in engineering workloads while simultaneously enhancing machine performance and resource availability through the evaluation and improvement of high-risk elements. The software consistently tracks failures identified during the FMEA process, providing users with detailed reports and visual representations that feature key metrics such as severity and risk priority, which pinpoint critical causes at any given time. Ultimately, this solution plays a vital role in bolstering product safety and dependability, which, in turn, fosters greater customer satisfaction and loyalty. Moreover, by streamlining the analysis process, it empowers teams to make informed decisions that contribute to continuous improvement.

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

Document Management Software facilitates the automation of various office tasks, enhances collaboration, streamlines document flow, and improves business processes. It also organizes quality control measures for both incoming and outgoing goods, which significantly reduces inspection times and minimizes costs. Furthermore, it offers comprehensive preventive maintenance management for equipment, ensuring optimal functionality. The tool allows for the meticulous documentation of meeting minutes and tracking of assigned tasks, while also supporting corrective actions, 8D methodologies, GAP Analysis, Kaizen proposals, FMEA, and Ishikawa diagrams. Additionally, it aids in the management of job descriptions, personnel records, announcements, suggestions, and complaints. Standardization of audit checklists and the documentation of conducted system audits, including 5S inspections, are also well-supported. Moreover, the software provides functionalities for the creation and management of Material Safety Data Sheets (MSDSs), ensuring compliance and safety across business operations. Ultimately, this comprehensive solution is designed to enhance efficiency and organization in all aspects of document management.

Monitoring quality risk effectively is challenging without a comprehensive knowledge management system. To tackle this, it is essential to establish processes that can proficiently identify, capture, manage, and disseminate vital documents and information. Sphera’s FMEA-Pro software provides a flexible framework that accommodates various FMEA methodologies, along with specialized features for managing risk data, ensuring that appropriate controls are implemented. This software connects essential quality information throughout design and manufacturing processes, facilitating the attainment of the expected quality standards set by your customers. Furthermore, Sphera’s FMEA-Pro software contributes to improving profitability by employing a uniform, standardized approach to thoroughly evaluate inherent risks. Additionally, Sphera's enterprise Advanced Risk Assessment empowers organizations to consistently pinpoint, evaluate, and mitigate the effects of operational risks effectively. By doing so, it enhances overall operational efficiency and resilience in the face of potential challenges.

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

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.

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

AutoDCP facilitates the linking of individual projects or specific operations into a unified composite project, which proves beneficial for integrating purchased components, various parts, or generic processes alongside part-specific details. This feature ensures that any changes in the foundational data automatically reflect in the composite projects. Furthermore, AutoDCP stands out as the quickest and most economical solution for sustaining an interconnected Process Flow Diagram, FMEA, and Control Plan. The inclusion of Risk Profiles streamlines the FMEA creation process, making it both efficient and rapid. Its user-friendly drag-and-drop interface simplifies the FMEA development experience, allowing users to navigate the system with ease. Additionally, AutoDCP is equipped with numerous features that significantly enhance productivity, demonstrating that the process of creating and updating FMEAs and Control Plans can be accomplished in a fraction of the time it would traditionally require. Ultimately, these advancements help teams focus more on analysis and less on administrative tasks.

We provide quality management software, offering comprehensive QM solutions tailored for all quality-related tasks, a tradition we've upheld for 25 years. As experts in the field, we have created a versatile quality management solution through our modular software, BabtecQ. Additionally, we present Babtec Qube, a cloud-based platform designed to facilitate collaboration with your suppliers and customers for effective management of your quality tasks. Our offerings empower you to visualize the complete spectrum of quality processes, both within your organization and with external partners, for a quality experience you will be eager to share. If you're interested in enhancing your understanding of quality management principles, you've found the perfect resource! Our knowledge pages offer insights into various topics, such as complaint management and the 8D report. Furthermore, the System FMEA, often referred to as system analysis, serves as a critical component of the FMEA (Failure Mode and Effects Analysis) process, focusing on the evaluation of an entire system to ensure that all individual components function together seamlessly. As you explore these resources, you will gain valuable insights into the intricacies of quality management, equipping you with the knowledge to implement effective practices in your organization.

Software that helps you comply with regulations. Fannie Mae, Wendy's and Walmart trust the best mobile inspection and audit platform. This will help you improve safety and accuracy. The #1 field management platform for teams, FORM OpX will transform your Excel, paper, and digital processes. FORM OpX combines advanced data gathering and configurable workflows with powerful operational insight to increase compliance in real time. To ensure compliance and team compliance, you can set up audits, inspections, or workflows. Digital forms allow you to capture data and guide teams to the right actions. Set up automated alerts and escalates to prompt corrective action when issues arise. You can save time and money by creating customizable workflows that improve processes, increase compliance, and reduce errors.

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

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

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

Transform your operations into a digital framework that prioritizes security, environmental responsibility, quality, and hygiene within your business. By centralizing, simplifying, and automating processes through a single tool, you can achieve sustainable performance for your organization. The effectiveness and safety of your enterprise hinge on streamlined automated processes, and BlueKanGo presents itself as the comprehensive digital EHSQ solution for managing these essential functions. If you're aiming to tackle societal and environmental challenges, mitigate risks, and enhance operational excellence, trust the platform that over 3,500 customers have relied on for more than 18 years. Embrace the digitization of your quality management, EHS initiatives, and much more, covering aspects like quality audits, employee health and safety, environmental compliance, CMMS, inspections, certifications, standards, corporate social responsibility, regulatory oversight, and strategic planning. Our six key differentiators highlight our strengths in the industry. With over 18 years in the market, BlueKanGo stands as a SaaS platform limited only by your creativity, offering an innovative, scalable, and comprehensive solution designed to adapt to your organization's evolving needs. The future of your business processes starts with a commitment to digital transformation and a partnership with BlueKanGo.

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

SoftTech Health provides an extensive array of quality management software solutions specifically designed for the healthcare sector today. By offering seamless integration, you can efficiently consolidate all your quality management activities into one user-friendly software platform. Our Accreditation Manager is designed to assist you in preparing for upcoming inspections, equipped with features that allow you to easily compare and transfer data from prior inspections. It automatically monitors compliance evidence, ensuring that crucial details are not overlooked. Each inspection requires careful attention to detail to guarantee that all requirements are met; it also aims to minimize the time spent on coordination, tracking, and reporting during audits, while simplifying the often tedious process of collecting supporting documentation. The Accreditation Manager not only streamlines these essential tasks but also enhances compliance and positively impacts your financial outcomes, demonstrating its value across multiple facets of healthcare management. Additionally, this software empowers organizations by providing insights that can lead to continuous improvement in quality management practices.

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.

Knowllence acts as a risk management integrator, providing software, training, and consulting services that ensure effective quality, safety, and environmental (QSE) risk management. Safeguard your employees by managing safety through comprehensive documentation, arduousness assessments, and chemical risk evaluations. Enhance your design process with robust methodologies like functional analyses, Failure Modes and Effects Analysis (FMEA), and Fault Tree Analysis (FTA). Ensure the reliability of your industrialization phase by utilizing tools such as AMDEC Process FMEA and establishing a meticulous monitoring plan. Align your risk control measures with ISO 14971 standards for the design and safety of your medical devices. Our team is adept at understanding your specific methodologies and can tailor the configuration of our software to align seamlessly with your existing standards and processes. We offer a comprehensive service designed to streamline your work sessions and risk assessments, empowering you to advance your projects while maintaining a sustainable system: you retain control over the study and the action plans within an efficient, user-friendly software environment. By partnering with us, you can enhance your organization's ability to manage risks effectively and ensure compliance with industry requirements.

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 SCIO™ software by PLATO has gained significant traction among professionals and facilitators alike. For those in the engineering sector, the web-based PLATO e1ns is highly recommended for its user-friendly design, making it accessible for all team members. This platform integrates the core functionalities of SCIO™ effectively. PLATO e1ns serves as a pivotal tool for enhancing the product development process (PDP), particularly during its initial phases where crucial decisions regarding cost and risk management are made. With e1ns, PLATO offers a solution that focuses on the foundational elements of PDP for optimal efficiency. The advanced database capabilities of SCIO™-FMEA meet the essential requirements for knowledge management, support multiple users, and cater to various languages. Furthermore, the SCIO™-Matrix provides a rapid approach to system analysis, enabling the transformation of customer needs into product features with effective execution. This comprehensive tool ensures meticulous planning and documentation of each process step, all of which are securely stored in the SCIO™ database, ready for future reference and use. In this way, PLATO empowers teams to streamline their workflows and enhance productivity throughout the development cycle.

With LINK Services, you have immediate access to test specifications, supplier communications, test failures, lab notifications, corrective actions, and performance metrics. This innovative application for managing Product Compliance Testing is designed specifically to streamline the processes involved in product and material testing and conformity. It offers supply chain partners a suite of tools to effectively organize and communicate about tasks and analytics related to testing programs, including test ordering, results, lab reporting, corrective actions, product certificates, bills of materials, and other crucial quality management activities. By connecting brand and retailer enterprise systems such as PLM and ERP/SAP with suppliers and testing laboratories—whether in-house or third-party—LINK simplifies and consolidates all relevant data into one cohesive, lab-agnostic platform. This ensures that all stakeholders can efficiently access and share critical information, ultimately enhancing collaboration and compliance across the entire supply chain.

You can now access your personal Quality Management Expert through an online platform designed for your convenience. With ready-to-use templates that can be seamlessly integrated into your organization, you can ensure efficient operations. Our offerings include comprehensive Quality Management Systems and digital solutions tailored for ISO 13485 related to Medical Devices, as well as ISO 9001 for General Quality Management, providing a robust framework for your quality assurance needs. Take advantage of our services to elevate your quality management practices to new heights.