Top ARMATURE Fabric Alternatives

Dot Compliance has introduced the first ready-to-use Quality Management Solution integrated with the Salesforce.com platform. This innovative solution encompasses a comprehensive array of pre-configured eQMS and compliance processes, allowing clients to implement it swiftly and affordably. Included in the Dot Compliance offerings are complete project validation services alongside product validation packages. Their solution stands out as the most economical option for quality and compliance management in the industry, empowering users to deploy adaptable and scalable solutions without delay. Key quality processes such as Document Management, Training Management, CAPA, Audits, Customer Complaints, Change Management, and Supplier Quality can be automated effortlessly. Furthermore, the solution is designed to be fully configurable and supports seamless integration, which makes it easy for customers to tailor the system to meet their unique specifications. By prioritizing user needs, Dot Compliance ensures a smooth transition and effective management of quality across various operations.

TLM QMS Software is an advanced and reliable platform for quality, risk, and material management that meets validation and 21 CFR Part 11 compliance standards. This innovative, comprehensive quality management system is designed for customization, allowing seamless integration with online CRM solutions, QuickBooks, or ERP systems. Total Lean Management (TLM) QMS Software aims to provide an economical and highly cohesive environment that is adaptable and continuously evolving, enabling the incorporation of specialized systems as necessary to develop a digital business ecosystem tailored to your organization’s workflow requirements. This flexibility ensures that the software can grow alongside your business, responding effectively to changing needs over time.

Streamline your quality processes with QT9's comprehensive cloud-based Quality Management System (QMS) Software Suite. Designed for ease of use, QT9 QMS features over 25 modules that offer unlimited scalability to meet your needs. Enhance your ISO and FDA compliance efforts with automated email alerts, task lists, and FDA 21 CFR Part 11 compliant electronic approvals. QT9 QMS empowers organizations in the Life Sciences, Biotechnology, Medical Device Manufacturing, and Pharmaceutical sectors to achieve digital transformation in their operations. Stay informed with real-time status updates and instantly visualize your quality metrics. The software includes essential features such as document control, revision management, corrective actions (CAPAs), and nonconformance tracking, among others. Additionally, it facilitates streamlined product releases with modules for Deviation Management, Engineering Change Orders, Failure Mode and Effects Analysis (FMEA), and Inspection Management. Transition to a paperless environment and automate your labor-intensive tasks effortlessly. QT9 QMS is ready for immediate use, allowing you to get started quickly. Experience it firsthand by signing up for a free product tour or beginning your free trial today at QT9qms.com. Embrace the future of quality management and elevate your organization's efficiency.

SimplerQMS provides a cloud-centric Quality Management Software tailored specifically for the Life Science sector. This innovative platform ensures adherence to an array of regulatory standards, 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, and is fully validated under GAMP5 guidelines. The software encompasses a comprehensive suite of Life Science QMS modules, including Document Control, Change Control, Training Management, Supplier Management, Complaints Management, Non-Conformance and Deviation Management, CAPA Management, Audit Management, Technical Documentation Management, Risk Management, and Quality KPIs, among additional functionalities. Moreover, SimplerQMS seamlessly integrates with Microsoft Office, enabling users to manage documents within familiar applications like Word, PowerPoint, and Excel. In summary, SimplerQMS not only streamlines operations through efficient, paperless workflows but also ensures that organizations can meet the stringent compliance mandates essential in the Life Science industry. Furthermore, its user-friendly interface and robust capabilities make it an indispensable tool for companies looking to enhance their quality management processes.

Qualtrax is an advanced software solution designed for quality and compliance that facilitates the management and control of documentation, automates essential business processes, optimizes training management, oversees both internal and external audits, and guarantees adherence to vital industry regulations in real-time. This software proves to be an essential tool for organizations operating within tightly regulated sectors that must comply with standards like ISO 17025, 17020, 13485, 9001, TNI, GFSI, FDA, and FQS. By integrating these functionalities, Qualtrax not only enhances operational efficiency but also helps organizations mitigate risks associated with non-compliance.

Virtual Atlantic's Jetpack Accreditation Management is an innovative tool crafted by accreditation experts specifically for those in the accreditation field. This unique solution offers complete customization to fit any accreditation procedure, making it unparalleled in its adaptability. Jetpack not only simplifies but also optimizes the entire accreditation journey, employing a centralized platform to automate critical tasks such as self-study submissions, annual reporting, site visit coordination, data visualization, benchmarking, and document archiving. This solution is versatile enough to conform to various accreditation protocols. Among its standout features are collaboration capabilities, compliance oversight, and user access controls. Additionally, it includes tools for self-assessment, management of substantive changes, and administration of site visits and calendars. Other important functionalities encompass document management, archiving and retention policies, survey integration, workflow automation, and management of certifications. The comprehensive design of Jetpack grants users exceptional command over any accreditation process, ensuring efficiency and effectiveness throughout. With Jetpack, organizations can expect a transformative approach to managing their accreditation needs.

Qualio serves as a comprehensive platform for managing quality and compliance needs, making it particularly suitable for expanding businesses in the healthcare and life sciences sectors. Not only is Qualio dependable and cost-effective, but it also boasts a user-friendly interface. This innovative tool enables companies to accelerate the development of life-saving products while ensuring full compliance with ISO, GxP, and FDA standards. By centralizing functions such as document control, training, non-conformance reports (NCRs), audits, supplier management, and handling complaints, Qualio simplifies the operational processes for its users. This integrated approach allows organizations to focus on their core mission of improving health outcomes.

Intellect's Quality Management System (QMS) software is demonstrated to enhance quality processes and decrease total quality expenses by as much as 40%. Crafted by certified quality experts, our applications are easily customizable thanks to a user-friendly no-code platform and drag-and-drop features. This contemporary and straightforward solution offers remote access for your team, mobile applications, dynamic workflows, analytics, and comprehensive reporting capabilities. The suite of applications encompasses Document Control, Employee Training, Audit Management, Corrective and Preventive Actions (CAPA), Nonconformance management, along with a range of other beneficial functionalities. With such a versatile toolset, organizations can streamline their quality management efforts and drive significant improvements across various operational areas.

SoftTech Health offers a broad spectrum of quality management software solutions tailored specifically for the healthcare industry. With its seamless integration capabilities, users can effectively unify all quality management functions within a single, intuitive software interface. The Accreditation Manager is particularly helpful in preparing for future inspections, featuring tools that facilitate the easy comparison and transfer of data from previous evaluations. It continuously tracks compliance evidence, ensuring no vital information is missed. Each inspection demands meticulous attention to detail to ensure all criteria are satisfied, while also aiming to reduce the time invested in coordination, tracking, and reporting during audits. This software simplifies the often laborious task of gathering necessary documentation. Beyond just streamlining these critical processes, the Accreditation Manager enhances compliance and positively affects financial results, showcasing its value in various aspects of healthcare management. Furthermore, by equipping organizations with valuable insights, this software fosters a culture of ongoing improvement in quality management practices, ultimately benefiting both staff and patients alike.

Introducing LearningBuilder, your dependable and scalable solution for managing certifications. LearningBuilder has been crafted to facilitate certification, licensing, and accreditation initiatives. Our expert team is equipped to address the distinct challenges faced in the credentialing industry. Over the last two decades, we've gained invaluable insights from our customers. As your technology partner, we are dedicated to maximizing the value of your software investment: - We will transform intricate requirements into a streamlined application process for candidates. - Our continuing education management solutions will make your recertification procedures more efficient. - We will enhance engagement with constituents through automated communications and timely reminders. In addition, we provide comprehensive reporting tools that make your program data both accessible and actionable. Are you prepared to experience a system packed with advanced features? With LearningBuilder's certification management software, you can finally eliminate the need for cumbersome manual workarounds, allowing you to focus on what truly matters in your certification journey.

SoftExpert EQM is a comprehensive enterprise quality management software (EQMS) that supports organizations in achieving and maintaining ISO 9001 certification by automating and improving quality processes tailored to their specific products, operations, and business methodologies. This flexible and modular platform consolidates all vital quality initiatives, which encompass process mapping and the management of documented information, such as standard operating procedures, work instructions, and records, in addition to handling non-conformance reports, corrective and preventive actions, and quality metrics. Moreover, the software adeptly manages supplier relationships, resolves customer complaints, conducts quality audits, oversees training and competencies, and assesses quality risks and controls, including quality inspections and statistical process control, thus fostering a more agile and robust quality management system. By optimizing these various functions, SoftExpert EQM enables organizations to significantly elevate their overall quality performance and regulatory compliance, ultimately leading to enhanced customer satisfaction and operational efficiency. This powerful tool not only streamlines processes but also provides valuable insights that help drive continuous improvement initiatives within the organization.

Transform your operations into a digital format by focusing on security, environmental concerns, qualitative measures, and hygiene standards within your business framework. Streamline and centralize your processes while automating tasks to enhance efficiency. With a single tool, you can effectively oversee your organization’s sustainability and overall performance. Automated workflows serve as the backbone of safety and productivity in any enterprise. BlueKanGo stands out as the comprehensive digital EHSQ platform designed for efficient management of these processes. For nearly two decades, BlueKanGo has gained the trust of over 3,500 customers, proving its reliability and effectiveness. This platform allows for the digitization of various aspects such as quality control, audits, employee health and safety, environmental management, CMMS inspections, certification compliance, corporate social responsibility (CSR), regulatory monitoring, and strategic planning. Six key differentiators highlight what sets BlueKanGo apart from its competitors. With a robust history of 18 years, BlueKanGo is a boundaryless SaaS platform offering an innovative, scalable, and all-encompassing solution for modern businesses. By choosing BlueKanGo, you are investing in a future-ready system that adapts to your evolving needs.

Software designed for regulatory compliance is essential for organizations like Fannie Mae, Wendy's, and Walmart, who rely on a top-tier mobile inspection and audit platform. By utilizing such tools, you can significantly enhance both safety and accuracy within your operations. FORM OpX stands out as the leading field management platform, revolutionizing the way teams interact with Excel, paper, and digital processes. It integrates sophisticated data collection alongside customizable workflows, offering vital operational insights that boost real-time compliance. To promote adherence to regulations, you have the option to implement audits, inspections, or tailored workflows. With digital forms, data can be captured effectively while steering teams toward appropriate actions. Automated alerts can be configured to escalate issues, ensuring timely corrective measures are taken when necessary. Through the creation of personalized workflows, you can streamline processes, enhance compliance, and minimize errors, ultimately saving both time and resources. This approach not only fosters a culture of accountability but also empowers teams to operate with greater efficiency.

Certdox is food safety management software designed for the everyday work of FSQA teams. Built by people who have worked in food manufacturing, it gives teams a clear, reliable way to manage compliance without the clutter of spreadsheets, binders, or disconnected systems. Certdox brings all your core food safety functions into one place. That includes document control, audit management, training records, sanitation tracking, supplier approvals, and task scheduling. Everything stays organized and accessible, whether your team is reviewing logs from a QA office or verifying forms on the floor. Unlike generic tools or bloated systems that try to do everything, Certdox focuses on what FSQA teams need most. It’s structured around the real tasks that keep operations audit-ready, from maintaining HACCP plans and preparing for certifications like SQF or BRCGS to managing supplier documents and staying ahead of corrective actions. Every Certdox plan includes all modules, with flat-rate pricing based on the number of facilities. There are no user limits and no surprise fees. This makes it easy to scale across locations, onboard new staff, and keep everyone working from a single source of truth. Certdox is cloud-based and runs in any modern browser. It requires no IT setup and can be implemented quickly with built-in templates and support. Whether your team is preparing for a third-party audit, updating SOPs, or managing day-to-day records, Certdox helps you stay compliant without slowing down your operation. It’s software built for food safety from the ground up. Practical, reliable, and built to help teams feel audit ready, every day.

ZenQMS enhances the quality compliance standards for life sciences organizations by utilizing a cloud-based platform specifically designed for this purpose. This platform streamlines processes such as document collaboration, control, training, issue management, audits, and change management. The team behind ZenQMS consists of experts in technology and quality who are united in their mission to elevate quality management to a fundamental aspect of business operations. Their innovative approach ensures that companies can maintain high standards while adapting to an ever-evolving regulatory landscape.

1factory's Manufacturing Quality is a flexible quality control software tailored for manufacturing enterprises, accessible in both cloud-based and on-premises formats. This powerful, reliable, and secure platform encompasses a multitude of features, such as first article inspections, factory oversight, quality control strategies, and a variety of inspection types, including in-process, final, and incoming inspections, in addition to thorough inspection management and corrective actions for any non-conformities. Furthermore, users can conduct metrics calculations for Process Performance (Pp, Ppk) and Process Capability (Cp, Cpk), effectively manage variation and SPC control, assess defect risks, and carry out numerous other vital quality management functions. The software's extensive range of functionalities not only streamlines quality assurance processes but also empowers manufacturing companies to continuously improve their performance and compliance standards. Consequently, its comprehensive capabilities position it as an excellent option for organizations aiming to bolster their quality management efforts.

uniPoint provides a versatile modular quality management software that functions on-site. This solution integrates effortlessly with multiple ERP systems, enhancing its adaptability. It serves manufacturers from various sectors and production techniques. Users can effectively manage processes such as document control, equipment management, non-conformance tracking, and the administration of corrective and preventive actions, ensuring thorough quality oversight. Moreover, the software's flexibility significantly boosts operational efficiency and ensures compliance across a wide range of manufacturing settings. Its robust features empower businesses to maintain high standards while adapting to ever-changing industry demands.

qmsWrapper is a comprehensive Quality Management Software designed specifically for small businesses and startups. This tool is ideal for organizations aiming to boost efficiency by adhering to ISO 9001:2015 standards, as well as for MedDev creators seeking to seamlessly navigate the requirements of ISO 13485:2016 and 21 CFR 820. It is particularly beneficial for businesses that require assistance in establishing and utilizing an effective, validated Quality Management System. Additionally, it serves companies looking to streamline their quality management processes by transitioning from traditional paper-based methods to automated solutions.

HQMS offers a diverse range of applications that can be deployed on-premise or accessed through hosting, encompassing features such as Document Control, Audits, Corrective Actions, Calibration, Training, Material Nonconformance, PPAP, Project Management, Risk Management, and the HQMS Supplier Portal. The platform boasts a strong technical foundation, with capabilities for configuration, personalization, and customization, along with flexible security options, compatibility with any HTML5 browser, and support for Single Sign-On, enhancing user accessibility. Additionally, it seamlessly integrates with ERP systems and other applications, making it versatile for various operational needs. The reach of HQMS extends across multiple sectors, including manufacturing industries such as Aerospace and Defense, Automotive, Consumer Products, Medical Devices, Food, and Energy, as well as healthcare, retail, non-profit organizations, and government entities. With a strong emphasis on security, the applications ensure that critical functions like Document Control, Audits, and Training are managed effectively, while also allowing for personalization and integration with existing systems. This comprehensive approach not only streamlines processes but also enhances overall organizational efficiency and compliance.

Simplifying document control is now possible, allowing you to create, review, approve, revise, and retire documents seamlessly. Every transaction is meticulously recorded with e-signatures and timestamps, all stored within the Audit Trail for complete transparency. The SOLABS QM10 Audit APP facilitates a comprehensive tracking system for your audits, encompassing everything from initial planning to final closure. Additionally, the SOLABS QM Essentials package enhances your reporting capabilities with its user-friendly and sophisticated tools. Monitoring trends and tracking progress are essential elements of an effective quality management system. The dashboards and reports are designed for ease of use, customizable to fit your needs, and can be conveniently shared in popular formats, including Excel, PowerPoint, and PDF. Reports and dashboards can be distributed across your organization with remarkable speed. Training management is also streamlined, enabling you to create, schedule, monitor, and assign training tasks within seconds. Online assessments are available to ensure your team's learning is validated effectively. With the SOLABS QM Training section, you can oversee every facet of training, making it an integral part of your quality management approach. Furthermore, this system supports continuous improvement by enabling feedback loops and ongoing evaluation of training effectiveness.

QEdge by Sarjen Systems is a robust and highly specialized Enterprise Quality Management System (EQMS) specifically engineered for the nuanced requirements of pharmaceutical manufacturing and the broader life sciences industries. This comprehensive solution is designed to meticulously address diverse quality challenges while ensuring unwavering compliance with stringent global regulatory standards such as FDA, EU-GMP, and ICH guidelines. QEdge significantly streamlines and automates a wide array of critical quality processes, including Change Control, Deviation management, Corrective and Preventive Actions (CAPA), efficient Document Management, and structured Training programs. It incorporates key features like robust SOP lifecycle management and SCORM-based eLearning capabilities, enhancing user experience and effectiveness. The system's design ensures audit-ready compliance tracking, contributing profoundly to operational excellence, impeccable data integrity, and regulatory readiness within demanding GxP environments. By facilitating superior process control, automating essential tasks like PQR/APQR, and simplifying vendor qualification, QEdge ultimately drives greater efficiency, mitigates risks, and elevates overall quality management throughout an organization's operations.

Paradigm 3 is an all-encompassing platform that caters to both web and desktop users, specifically designed to support businesses in managing compliance with a strong emphasis on Document Control, CAPA Compliance, and Competency Tracking and Training. The software boasts a plethora of features, such as an event manager to oversee incident investigations and customer complaints, notifications for tasks delivered via email, and audit preparation tools, among various others. Various sectors, including Healthcare, Manufacturing, Test Labs, and Service Industries, find significant advantages in utilizing the capabilities offered by Paradigm 3. This cutting-edge solution allows organizations to reduce reliance on multiple additional modules necessary for meeting compliance standards. The platform comprises four main modules that include more than 50 standard forms aimed at covering all facets of Quality, Safety, and Environmental management. Additionally, the form designer functionality grants users the ability to craft personalized forms or alter existing ones, ensuring that every unique requirement is met with precision. This adaptability in form customization not only elevates the platform's effectiveness but also establishes it as an essential resource for businesses committed to achieving compliance excellence. Ultimately, Paradigm 3 serves as a vital tool in navigating the complexities of compliance management.

ZipQuality delivers a software-centric service aimed at assisting medical device manufacturers in the successful launch of pioneering products. Our collaborative platform skillfully handles rapid design changes for agile teams while ensuring compliance with regulatory requirements. Featuring a pre-configured system that integrates essential processes and tools, there's no need for alterations to your established quality system. The unified platform effectively supports quick design revisions for product documentation, maintaining consistency throughout. Our experienced consultants provide guidance to your team at every stage of the journey. Built upon the powerful ENOVIA platform, our extensive and scalable software solutions are customized to cater to your specific needs. This integrated approach enables swift design modifications while guaranteeing that product documentation and data are kept in sync, ensuring that all records are audit-ready. We address critical aspects such as product specifications, hardware, and software requirements, with a deep understanding of the challenges posed by software-intensive medical devices. The ZipQuality framework is designed around a methodical documentation strategy that strengthens systems engineering, fosters robust risk management, and guarantees clear traceability, thus becoming an essential tool for any medical device enterprise. Furthermore, our dedication to continuous enhancement ensures that we consistently refine our service offerings to stay in line with the latest developments in the industry, providing added value to our clients. In this ever-evolving landscape, having a partner like ZipQuality is crucial for maintaining a competitive edge.

By integrating your Quality, Health, Safety, and Environmental Management systems into a Cloud-based platform and a Mobile App, you can significantly boost the efficiency of your organization. Clients from a wide array of sectors and geographical locations, such as the United Kingdom, Australia, New Zealand, and South Africa, rely on Mango for their QHSE compliance. Our commitment to quality management and information security is reinforced by our ISO 9001 and ISO 27001 certifications, which offer peace of mind to our clients. Utilizing Mango allows your consulting firm to tap into new recurring revenue opportunities while delivering exceptional value to your clients, effectively distinguishing you from your competitors. The Cloud-based framework of Mango signifies its role as a pioneer in the future of compliance management within the industry. With Mango, you can provide your clients with a more efficient and cost-effective method for meeting their compliance needs, while also simplifying their operational processes. As a leading Compliance Management solution developed by Mango Limited, it continuously adapts to satisfy the evolving needs of diverse organizations, thereby ensuring its relevance in a rapidly changing landscape. This adaptability not only enhances user experience but also fosters long-term partnerships built on trust and reliability.

To accelerate the launch of new products while ensuring compliance with international standards, businesses need to optimize and automate their processes for collecting, monitoring, analyzing data, and tackling associated issues. QUMAS EQMS, formerly known as ProcessCompliance, is a cloud-based solution crafted for Enterprise Quality and Process Management, providing comprehensive integrated tools for managing regulatory, quality, and compliance aspects within a validated Quality Management System (QMS) framework. Utilizing QUMAS’s data-driven approach, organizations can proficiently handle quality-related information and easily access valuable quality data, which guarantees a clear view into their quality environment. In addition, QUMAS offers interactive quality dashboards that summarize QMS performance across different business sectors and quality initiatives, enabling users to visualize progress effectively. The platform allows for the generation of reports that can be exported, shared through email, or scheduled for regular updates, making it a versatile tool for communication. Moreover, it supports secure, efficient, and compliant information sharing among departments involved in QMS, thus fostering collaboration and improving operational efficiency. Ultimately, QUMAS equips organizations to achieve their quality goals while adeptly managing the intricacies of regulatory compliance, positioning them for success in a competitive landscape.

We Are the core competencies that propel your operations forward! You can effectively oversee your crucial skills and allocate your teams in a strategic manner. eLamp is designed as a holistic solution that encompasses various industries. Be it for business divisions, human resources, or IT management, eLamp's uniqueness is rooted in its commitment to improving HR functions and operational effectiveness through adept skill management. This platform is specifically crafted to address the distinct challenges encountered by different business units, subsidiaries, or sectors, guaranteeing that we serve their particular needs with a focused approach. In addition to this, our platform simplifies the upkeep of necessary regulatory skills, making certification and compliance more manageable. Handling certifying and regulatory competencies can be complex, but our Skill Master interface allows you to tailor all related regulations, which include personalized skill lists for employees, diverse timelines for skill obsolescence, various protocols for loss and discount, cascading competence loss management, assigned training responsibilities, and specific evaluation tasks. Moreover, it supports the creation of official documents and forms, helping to ensure that your operations stay compliant and effective. By utilizing eLamp, your organization can elevate its skill management capabilities to not only fulfill regulatory requirements but also boost overall efficiency and productivity, setting a new standard in operational excellence. This comprehensive approach not only enhances compliance but also empowers your teams to perform at their best.

Elevate your team's comprehension of policies and procedures, along with the motivations that drive them, through the engaging and informative eLearning platform offered by VigiTrust. This platform encompasses vulnerability scanning, assessment, and reporting, utilizing questionnaires, surveys, and check-sheets to generate thorough, interactive reports and visual data representations. By employing a cohesive program and platform, organizations can maintain consistent compliance with various regulations and standards, including GDPR, PCI DSS, and ISO27001. VigiTrust is recognized as an award-winning provider of Integrated Risk Management (IRM) Software as a Service (SaaS) solutions, catering to clients in 120 countries across diverse sectors such as hospitality, retail, transportation, higher education, government, healthcare, and eCommerce. Their innovative solutions empower both clients and partners to effectively prepare for and ensure adherence to legal requirements and industry standards related to data privacy and information governance. In addition to fulfilling compliance obligations, leveraging VigiTrust's extensive tools allows organizations to cultivate a robust culture of security awareness and proactive risk management among their workforce. By doing so, they enhance not only their security posture but also their overall operational effectiveness.

Cloud-based Enterprise Quality Management Software designed specifically for the life sciences industry is crucial for successfully navigating the complexities of today's operational environment. By placing technology at the center of operations, it enables quality assurance teams to be swiftly alerted to emerging issues, which cultivates a proactive management culture. Organizations that achieve a comprehensive understanding of their quality management system's performance in relation to operational conditions can effectively mitigate risks and sidestep costly delays. Montrium has developed its Enterprise Quality Management System (EQMS) with the specific aim of assisting life science companies in tackling their unique quality management hurdles, especially in the area of content management. Our SharePoint QMS modules are crafted with adaptability in mind; they can operate autonomously or integrate seamlessly into a unified quality management system. Accessible via our Montrium Connect Platform, these modules can be deployed either on-premises or through cloud-based solutions, making them particularly suitable for pharmaceutical companies, contract manufacturing organizations, and medical device manufacturers. Each module is carefully constructed to ensure adherence to Good Manufacturing Practices (GMP) and Good Clinical Practices (GCP), thus helping organizations uphold the highest standards of quality. This all-encompassing approach not only boosts operational efficiency but also fortifies the integrity of the quality management process, reinforcing the commitment to excellence within the life sciences sector. As a result, companies can better navigate regulatory landscapes while achieving their business objectives.

The Intact Platform is a comprehensive Enterprise Resource Planning (ERP) solution available both in the cloud and on-premise, making it the ideal choice for audits, assessments, certifications, accreditations, and various standards. Unlike other audit collection tools, it provides an all-encompassing approach that facilitates the management of communications, business objectives, and personnel. With its unmatched capabilities, the Intact Platform features a fully integrated modular workflow that can be easily scaled to meet diverse needs. Users can expect an average efficiency increase of 34%, with potential gains exceeding 60%. Its exceptional modularity, flexibility, and scalability set it apart from competitors, while supporting all standards and audit services. Additionally, the platform operates through a digital workflow, eliminating the need for paper and enhancing both remote and on-site auditing experiences. It effectively manages non-conformities and corrective actions, while also enabling risk-based audit planning. Communication with clients is seamless, and the platform excels in reporting and business intelligence (BI). Centralized data management, including a comprehensive audit trail, ensures that all information is readily accessible, allowing for continuous innovation and improvement in auditing processes. As a result, the Intact Platform stands out as a vital tool for organizations striving for excellence in compliance and operational efficiency.

Our digital eAccreditation platform boasts an all-encompassing workflow system, secure functionalities based on user roles, and communication tools designed to optimize business operations and improve teamwork. Liaison offers substantial support and training, in addition to providing online resources for best practices and customized consulting services to address your specific needs, which ultimately reduces administrative burdens and enhances outcome quality. With all essential documentation accessible online in real-time, participants are empowered to monitor progress effectively and tackle issues promptly as they arise. The eAccreditation system can be tailored to fit the distinct processes of each agency, featuring practical tools such as checklists, alerts, reminders, and notes that facilitate collaboration and boost efficiency. Agencies can swiftly integrate the system by creating the required modules throughout the accreditation journey, allowing for a personalized approach that accommodates the unique workflow of each organization. This adaptability not only allows agencies to choose the modules that best enhance their operational effectiveness but also ensures a more efficient and seamless accreditation process overall. By streamlining these functions, the platform significantly contributes to elevating the overall standard of accreditation practices.