QMS Alternatives

Interfacing’s Digital Twin Organization software provides transparency and Governance to improve Quality, Efficiency, and ensure Regulatory Compliance. Map, analyze, and automate processes, manage regulatory compliance, assess risks within a single platform! Interfacing’s digital twin solution (Enterprise Process Center - EPC) is an enterprise management system that helps companies digitalize processes to streamline operations, increase productivity, and continuously improve. Interfacing’s digital business platform – Rapid Application Development (RAD) Tools, with its Low-Code Development methodology will optimize usage of your technical resources and maximize transparency for ongoing improvement. Discover how our Low-Code Rapid Application Development module provides all the tools to create and deploy Custom, Scalable, Secure, and Mobile ready Applications in Days vs. Months!

QVscribe, QRA's flagship product, unifies stakeholders by ensuring clear, concise artifacts. It automatically evaluates requirements, identifies risks, and guides engineers to address them. QVscribe simplifies artifact management by eliminating errors and verifying compliance with quality and industry standards. QVscribe Feature Spotlights: Glossary Integration: QVscribe now adds a fourth dimension by ensuring consistency across teams using different authoring tools. Term definitions appear alongside Quality Alerts, Warnings, and EARS Conformance checks within the project context. Customizable Configurations: Tailor QVscribe to meet specific verification needs for requirements, including business and system documents. This flexibility helps identify issues early before estimates or development progress. Integrated Guidance: QVscribe offers real-time recommendations during the editing process, helping authors effortlessly correct problem requirements and improve their quality.

Dot Compliance provides the industry’s first off-the-shelf QMS solution – ready to deploy from day one, with little to no setup required, while also incorporating industry best practices and standards that address the latest global regulatory requirements. Powered by the Salesforce.com platform, our solutions enable life science organizations to quickly digitize their quality and compliance processes including Document Management, Training Management, Change Control, CAPA, Customer Complaints. Compliant with 21 CFR part 11, EU-Annex 11 and support ISO 9001, 13485, 14971, 27001 & MORE! Processes included: ▶ Document Management ▶ Training Management ▶ Quality Event Management ▶ CAPA Management ▶ Change Management ▶ Complaint Management ▶ Audit Management ▶ Supplier Quality Management ▶ Risk Management ▶ Design Control ▶ Deviations/Non-conformances ✔ Seamless Install ✔ Cost Effective ✔ One-Stop-Shop

Qualityze is a leading provider of enterprise quality management solutions, utilizing the Salesforce.com Technology Platform to build our EQMS Software solutions. Our team is 100% devoted to quality processes, compliance, and regulatory guidelines to address our customers' business environments. We do not distract ourselves with custom work or quality concerns. The idea of helping our customers create a culture of quality is not a new concept, but the way we developed our application, Quality Management Software, based on making it easy to use, intuitive, and inclusive. Therefore, the entire organization is involved in quality, not because they are told they should, but because it's easy, fun, and has a logical flow. We strive to optimize quality with excellence through our exclusive range of smarter quality management software solutions.

SQCpack by PQ Systems is a robust statistical process control (SPC) application that helps businesses analyze their data, understand and improve their processes, and communicate important quality information. SQCpack combines powerful SPC techniques, flexibility, and easy deployment and operation, which helps optimize process performance and productivity. SQCpack is easily scalable, whether for use on a single line or in a global multi-site operation. Organizations worldwide have selected SQCpack to harness the power of data analysis to increase customer satisfaction, improve audit success, and meet quality compliance requirements.

Intellect QMS is the latest version of Intellect's flagship product designed to help organizations and quality leaders meet FDA, ISO, and other global GxP regulatory compliance requirements. Intellect offers faster implementation time, robust out-of-the-box QMS capabilities, and extreme configurability to modify or build new apps. Empower your onsite and remote workforce with virtual auditing, online approvals, 21 CFR Part 11 electronic signatures, and ensure your team can access only approved and up-to-date quality documents, data, reports and analytics anytime, on any device. Intellect’s Environmental, health, safety and quality (EHSQ) software acts as a data management system for capturing, storing, and analyzing information related to occupational health and safety, waste management, and sustainability. It aims at reducing operational risk and improving health while attaining sustainability goals.

Managing a stability study is a complex process and mistakes can occur. Using a manual paper based system increases the risk of errors. The only solution is to implement a software based process that automates your stability studies and shelf-life analysis. Stability studies are highly scrutinized by regulatory agencies. Companies must be able to prove the validity of their data. Automated solutions provide the ability to produce the necessary documentation in real-time to satisfy auditors. Systems like Nova-Stability helps companies maintain regulatory compliance while reducing risk to the patient. Nova-Stability is a powerful process based feature-rich system that manages the entire stability testing process. This comprehensive solution is compliant with current regulatory guidelines on a global level. Nova- Stability accommodates all types of stability studies.

Arena’s product-centric quality management system (QMS) software enables medical device manufacturers to deliver safe and compliant products to market fast. Arena QMS streamlines new product development and introduction (NPDI) by connecting quality and product processes. Arena QMS ensures regulatory compliance to quality standards and regulations including FDA 21 CFR Part 820, Part 11 and ISO 13485. Arena QMS enhances visibility and traceability by controlling quality processes in context with bills of materials (BOMs), SOPs, DMRs, DHFs, specifications, drawings, and training plans.

Reva QMS is a software-based Quality Management System. Our solution is designed to help organizations collect, organize, manage, and report on their business-critical documents while aligning their business processes to comply with relevant industry standards, specifications, laws, and regulations. Specifically designed for highly regulated industries, Reva QMS helps organizations automate and streamline their paper processes for increased efficiency and regulatory compliance. It provides a comprehensive set of out-of-the-box functions and capabilities specifically designed for highly regulated industries to help them achieve greater operational transparency and comply with rules and regulations, policies, best practices, and industry standards. It provides an easy-to-use browser interface that allows users to manage critical business processes easily and in a simple manner.

QIMAone enables global brands, retailers and manufacturers in consumer good industries to digitize their quality and compliance operations, collaborate with key partners across their entire supply chain and collect reliable data to minimize disruption, increase visibility, and drive continuous improvement. Digitize your quality management, connect to your supply network and collaborate with suppliers to prevent defects. Onboard suppliers and inspectors, assign inspections and follow corrective actions collaboratively. Import, create custom workflows and checklists for inspections and audits. Consolidated actionable KPIs and benchmark to boost your supply chain. Visualise your supply chain and leverage risk-based strategies to drive proactive improvement programs. Reduce costs and save time to focus on value-added activities using standardized processes and automation. Empower your vendors and factories with actionable insights, e-learning content and collaborative tools.

Systematic Safety Management, Compliance Monitoring and Quality Management are not only a legal requirements for commercial air operators but also increase the efficiency of the organization, save money and thereby make the operation more profitable.If you still manage your safety, compliance and quality requirements using generic software tools and paper-based processes, you are missing out on significant efficiency savings that an electronic solution like Qperfect IAMS can realize.

To bring new products to market as quickly as possible in compliance with global regulations, organizations need to standardize and automate their business processes that manage the collection, tracking and analysis of information and the resolution of related issues. QUMAS EQMS (formerly ProcessCompliance) is a cloud-based solution for Enterprise Quality and Process Management that delivers comprehensive integrated regulatory, quality and compliance management capabilities in a validated QMS environment. QUMAS’s data-centric approach allows you to flexibly manage quality content and to access and re-use all quality data, providing comprehensive visibility into Quality. QUMAS’s interactive quality dashboards provide QMS overview across business areas and quality initiatives. Reports are available for export, email and scheduling. QUMAS allows QMS departments to exchange information securely, efficiently and compliantly in the cloud.

If you’re relying on multiple software and/or paper-based solutions to manage your compliance and manufacturing process needs, InstantGMP™ could be the key that unlocks the next level of success for your business potential. Seamlessly maximize production uptime, improve batch quality and meet all FDA compliance needs—and more—all with an affordable, paperless, all-in-one software solution. InstantGMP™ products work individually and together based on your business needs to deliver comprehensive, integrated software solutions that ensure end-to-end quality, consistency and GMP compliance. We’ll help you pick the right solution set for your business needs today, and tomorrow. Organize, manage and document batches electronically while reinforcing good manufacturing practices. Inventory Management Solution that meets Part 11 and GMP requirements. Complete quality system that comes with SOPs, templates and guided workflows - ideal for virtual biotech.

The transition to a paperless shop floor is seamless with TIPSFE Shop Floor Execution. Complete visibility into the inspection process and inspection documentation history allows manufacturing and quality teams to work together for greater control of the manufacturing process, and immediately identify potential for costly errors without slowing down production. This comprehensive approach gives companies the opportunity to save money by eliminating manual paper-based processes, reducing redundant data entry and improving efficiencies by sharing data across the enterprise. Having a software solution that provides the ability to identify and track issues on the shop floor is a significant competitive advantage that can greatly increase a company’s profitability and can deliver a significant return on investment year after year.

Plex Quality Management System (QMS) helps process and discrete manufacturers meet strict industry and customer compliance with a closed-loop digital system of record. Ensure predictable, repeatable quality delivery through in-line quality, clear reporting, and simple audit tracking. Meet industry compliance and customer regulations with quality documentation available in real-time, digitally, across the enterprise. Drive new and repeat business growth with on-time delivery performance, improved supplier management, and increased customer satisfaction. Making quality management inherent to your workflows and processes reduces quality loss and risk of warranty issues or recalls, improving your brand reputation and customer relationships. With Plex quality requirements and documentation are available and shared in real-time across the enterprise. Plex helps you generate process control plans with detailed inspection instructions and digital checksheets.

Compliance software that drives operations. Improve safety and increase accuracy with the top mobile audit and inspection platform for teams trusted by Walmart, Wendy’s, and Fannie Mae. Upgrade your paper, Excel, and digital processes to the #1 field management platform for teams. FORM OpX combines advanced data collection and configurable workflows with powerful operational insights to boost compliance in real-time. Configure audits, inspections, and workflows to ensure teams consistently follow procedures and meet regulatory obligations. Capture data instantly with digital forms that guide teams to the right action. Configure automated alerts and escalations to trigger corrective action as soon as issues arise. Save time and money with customizable workflows that improve processes and increase compliance — everywhere.

Is your quality management program working? Screening a small percentage of calls may leave non-compliant interactions hidden, and risk fines, lost business or worse. Verint can help. Most contact centers only review between 1 and 3% of calls. This severely limits your ability to identify risks and manage quality and compliance. Verint Automated Quality Management can automate the whole quality management process and help you achieve better compliance. Evaluate calls, identify non-compliance and assign coaching—for 100% of voice and text interactions. In this way, you will quickly gain a new level of insight into your organization’s standards of service and compliance. This helps you identify employees that need coaching to improve, and reveals any procedural steps that cause compliance and/or quality issues.

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

Replace paper with the next-generation visual inspection platform that shows workers exactly what to do, when they need to do it, keeping equipment operating and production quality high. Paper checklists are slowing down production, quality control, and equipment maintenance. ROO.AI replaces paper by combining a breakthrough visual interface with guided work instruction and Bots on standard mobile devices to increase frontline productivity and accuracy while helping companies onboard faster and upskill their workforce. Improve inspection processes, simplify process audits, speed up production lines, and ensure preventive maintenance. ROO.AI bridges the skills gap and drives continuous improvement in industries like manufacturing, energy, transportation, and more. Cut inspection times by up to 70% and automate data collection providing instant visibility to defects for quality checks and process audits.

qmsWrapper is an interconnected Quality Management Software for startups and small businesses. It helps all companies that want to increase productivity with ISO 9001:2015 and MedDev creators to easily achieve and manage ISO 13485:2016 and 21 CFR 820. At qmsWrapper, we cater to each industry’s unique quality management needs with tailored features: Compliance Made Easy: Adhere to standards like ISO 13485 and ISO 9001 effortlessly, maintaining a robust QMS. Risk Management: Simplify risk assessment with ISO 14971-compliant tools, effectively mitigating risks. Document Control: Intuitively manage documents for enhanced traceability and version control. Cloud-Based Accessibility: Access your QMS anytime, anywhere. Electronic QMS: Embrace efficiency with digitized QMS for faster approvals and real-time updates. Audit Management: Prepare for audits confidently with scheduling, tracking, and reporting tools.

The Secure Audit, Risk, Compliance & Quality Software. With On-Premise and Cloud-based deployment options. Auditrunner offers granular encryption and role-based access control for audit files and documents at-rest. All data transfers are protected. We have automated 3000+ business processes for enterprises around the world. Our GRC platform modules are just a few of them. Cloud-based or On-Premise, deploy and start using. Hassle-free integration process enables you to enjoy the benefits of the platform within weeks of kickoff . The low-code platform we are built upon is fully customizable and allows for compliance with any standard or regulation. Operate in a responsive manner in today’s fast-moving, ever-changing regulatory environment and comply with multitude of different legislation instantly without the need for assistance. The ease of use we offer is unmatched.

Inspired by people and technology, Quality Link 7 builds on our experience and proven platform for helping organizations automate processes, save money, and achieve regulatory compliance with an easy-to-use business operating solution. Quality Link delivers improved efficiency while eliminating manual paperwork with our document management. Every document you create will be stored and managed from within this module. You can print “uncontrolled” copies of your documentation from within this module, as well as perform many other document-related activities. With the enhanced organization, you’ll see clerical tasks by quality personnel reduced by up to 90 percent. Our software effortlessly converts existing documentation from your previous management system, and there’s no learning curve. But you won’t miss your favorite applications, as they can be easily integrated. With Quality Link, you can say good-bye to manual document maintenance, which requires constant monitoring.

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

Incomplete dynamic fields, overcommunication, and missed deadlines are just a few issues that can arise without an adequate Quality Assurance (QA) process in place. As privacy laws continue to develop and, at times, transform entirely, it becomes increasingly important to adhere to privacy legislation internationally. That’s why Munvo’s CampaignQA© ensures ongoing compliance to required regulations. This technology serves to complement your marketing automation system and improve overarching marketing execution processes in a timely fashion. Automate validation of inbound and outbound marketing campaigns and monitor the results with robust alerting and reporting features. Manage contact frequency controls with an easy-to-use, drag-and-drop interface (no coding required). Enable a rules-based validation approach for marketing data / marketing datamart quality.

The InterLink platform is the oil and gas industry’s leading web-based quality management software designed specifically for the administration of the API Spec Q1-9th Edition standard. The InterLink platform contains more than 64 integrated modules and built-in reports that enable users to control all aspects of the API Spec Q1 requirements from a single, secure, and easy-to-use oil and gas compliance tool. Organizations of any size can benefit from the increased productivity, efficiency, and security of adopting our InterLink oil and gas QMS software. Spreadsheet management solutions or manual templates result in cumbersome, isolated systems that fail to ensure the operational excellence of every product, facility or location. ​With the InterLink API Spec Q1 quality management software, you have the ability to host all your process quality records and compliance information on a single secure server, accessible from any web-enabled device or location.

Maintaining consistent product quality and quality processes can be challenging in today’s pharmaceutical manufacturing environments. Regulated industries such as the Pharmaceutical, Biotech and Life Sciences are required to maintain Good Manufacturing Practices (GMP) to meet regulatory requirements. Not only do you need to meet GMP requirements you must also be able to prove this. Using paper-based forms, disconnected systems, or manual processes to manage, track and report on quality issues and actions does not provide effective solutions for implementing harmonized, integrated quality management processes, which follow industry best practices.

QEdge QMS for Enterprise Quality Management Software (EQMS) system that optimizes the quality of various processes and ensures regulatory compliance. Enterprise Quality Management Software (EQMS) system reduces the risk of quality process failures; lowering overall costs and making the organizational processes more compliant. QEdge, as an EQMS accommodates companies in a disciplinary regulatory environment to make Quality Management System more robust and well managed by bringing all the quality processes such as Change Control, Deviation, Investigation, CAPA, Market Complaints, OOS, OOT, Risk Assessment, Document Control activities, Training Records and many more on a single platform. QEdge is an intuitive and highly configurable software platform to manage various regulatory, and nonregulatory business processes that facilitates error-free, cross-functional communication and collaboration with Quality management as a base and can interface with the legacy systems.

iCompliance is a comprehensive digital platform designed to streamline Quality, Health, Safety, and Environment (QHSE) management, Environmental, Social, and Governance (ESG) initiatives, and Governance, Risk, and Compliance (GRC) processes for organizations across various industries. Our software offers tools for incident reporting, risk assessments, audit management, corrective actions, and more to ensure compliance with regulations and standards, promote safety and environmental responsibility, track ESG performance, engage stakeholders, and manage regulatory requirements, internal controls, and risk mitigation strategies. With customizable workflows, real-time analytics, integration options, mobile accessibility, and multilingual support, iCompliance empowers organizations to achieve operational excellence, mitigate risks, and drive sustainable growth.

Compliance Management Software for the Cannabis Industry. Optimized Cannabis Compliance Software. ​The medical cannabis industry is highly regulated. Most states require cultivators, processors, and distributors to keep track of every seed, ounce of flower, and edible they sell or discard for quality issues. To stay on the right side of the law in the cannabis market, you need to have a paper trail for all transactions from the cultivation to the final sale. ​Constant shifts in an ever-evolving medical marijuana marketplace, coupled with the need to ensure compliance and reduce risk can no longer be managed with traditional software or manual templates alone. Features You Need to Succeed. ​Otter Systems Compliance Management Software provides a centralized platform for tracking regulatory requirements, organizing compliance documentation, and managing compliance processes, with features including: Cannabis Document Control, Policy Management, Change Management, Supply Chain Control.

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

Enabling a digital quality ecosystem to deliver the promise of proactive quality. TrackWise Digital is an industry-leading, cloud-based quality management system with integrated modules that work together to support quality, compliance and more efficient and effective decision making. With reporting and advanced analytics across all quality processes, users can leverage quality data to strengthen their culture of quality and impact company-wide performance. Based on Sparta’s 25+ years of experience, TrackWise Digital’s Quality Process Accelerators (QPAs) provide rapid value and streamline end-to-end digital quality. TrackWise Digital is the industry’s first QMS to leverage AI for enhancing quality related decision-making capabilities, providing a shift from reactive to proactive quality.

AURA is a web based QMS software that helps organizations to effectively monitor and manage your quality compliance activities. We bring you organization-specific quality management system and enable you to streamline your quality process for better risk management and assured compliance. With aura audit management software, you can maintain quality standards specific to different business areas within the enterprise.

OurRecords offers a secure, cloud-based credential and document management solution for businesses in the food, mortgage, and healthcare industries. With OurRecords, companies can take advantage of a centralized platform for storing, managing, and enabling access to verified credentials and records. Top features include supplier/vendor management, workforce prerequisite program, proactive alerts/notifications, document distribution, centralized documentation, and automated reports. Automate the distribution of required organizational and product compliance documents to your customers, auditors, and state regulators. Centralized Location for all your Standard Operating Procedures, Policies, Quality Programs, Certifications, Production Specifications, and other compliance documents. Automated alerts proactively notify suppliers, vendors, contractors, and staff of current and pending non-compliance issues that require attention.

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

Improve incoming parts quality and supplier quality performance,reduce the risk of production interruption, optimize the total cost of ownership, and manage supply chain risks. Monitor the in process quality performance and change of the trend through the whole flow of production, take preventive actions to reduce failure rate. Manage and control the quality of to-be-shipped out products, improve product competitiveness. Customer focus. Quick response to customer complaints, Improve the service and quality, improve customer satisfaction. Record and follow up corrective action and preventive actions.Realtime display of the task progress of each member.Enhance the capability of continuous improvement and improve corporate quality management system. Reduce the time on preparing audits, Improve the efficiency and effectiveness of audits. Mechanism in place to facilitate the audit as scheduled to be compliant with the requirements and regulations.

Digitize your processes. Security. Environment. Quality. Hygiene. Of Business. Centralize. Simplify. Automate. One tool to manage everything. For a sustainable performance of your organization. The performance and safety of an organization is based on automated processes. BlueKanGo is the digital EHSQ solution to manage them. Whether you are looking to address societal and environmental issues, minimize your risks, improve your operational excellence, rely on the solution approved by more than 3500 customers for more than 18 years. Digitize your Quality, EHS and more processes. Quality & audits management. Health and Safety of employees. Environment. CMMS & inspection. Certification, Standards. Corporate Social Responsibility (CSR). Regulatory Watch. Strategic Planning. 6 differences that are our key strength. With more than 18 years of existence, BlueKanGo is the SaaS platform that has no limits but your imagination. An innovative, scalable and all-inclusive solution

Defect-free business processes lead to defect-free products. And that is exactly why CASQ-it is designed to encompass all the steps in your quality assurance and quality management processes – starting with the development process, continuing through the material process – up to and including your support processes. The advantage of CASQ-it lies right here in this process-oriented mode of operation – functionality that enables your CAQ system to adapt flexibly to your processes – and not vice versa. CASQ-it supports your quality assurance processes on their journey into the future: Quality and reliability increase customer satisfaction whilst reducing the cost of quality. Each separate CASQ-it module functions independently – enabling you to optimize individual processes and workflows within your company right from day one. Our modules can be flexibly combined – or used to create a comprehensive quality assurance system.

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

SoftTech Health offers the most comprehensive suite of quality management software tools available in healthcare today. And since they integrate seamlessly, you’ll be able to streamline all your quality management tasks within one easy-to-use software package. Our Accreditation Manager helps you manage any upcoming inspections with tools to help you compare and copy over existing work from previous inspections. Automatically track proof of compliance and ensure nothing falls through the cracks. With every inspection, you want to: make sure that none of the requirements fall through the cracks; cut time to coordinate, track, and report on the audit; and streamline the time-consuming process of gathering your supporting evidence. The Accreditation Manager automates all these processes, improving both compliance and the bottom line at the same time.

Software & Services that keep the workplace safe, compliant, and your employees well trained. For more than two decades, SMG has been a trusted partner for process management, improving workplace safety, and ensuring OSHA and other regulatory compliance on local, state, and federal levels for businesses ranging from food service distribution centers and restaurants to LTL freight carriers. SMG’s software-driven expertise in health and safety management empowers your business to easily ensure compliance, reduce costly incidents, and improve operations and logistics. Replace generic policy documents and overlooked safety plans with action- driven software tools that seamlessly integrate with processes for training employees, conducting safety audits, reporting incidents, and taking corrective action.

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

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

Every organizational structure is unique, requiring a custom tailored approach when dealing with concerns related to international standards. More often than not, this is a time intensive process. To address these needs, ISMS Solutions offers Conformance Works, a proprietary platform that walks customers through an automated system assisting customers with becoming compliant with whatever ISO standard they need. Simply put, Conformance Works simplifies and customizes the standard certification approach for each organization. With a built in document management system, global change editor, compliance management system, and risk assessment module, company documentation becomes straight-forward and efficient. The software will be accessible via multiple digital methods. Allows faster implementation of ISO standards for certification. Provides a streamlined user experience to meeting or exceeding ISO standards.

Ultimately records of all risk management activities must be kept and they need to be readily available for inspection. Most healthcare leaders know that their accreditation both legally and morally compels them to implement risk management. Yet, most have not as this was loosely enforced. The Omni-Assistant is a sophisticated modular enterprise system. It is highly intuitive, fully integrated, streamlined and optimized to support best business practices with full quality compliance to regulatory bodies. The Omni-Assistant Core is the predominant module that bridges and successfully connects all the modules. Enabling seamless integration, the processes are activated from one module to another based on specific business rules. The robust workflow engine design efficiently initiates processes and formulates triggers and events based on your business needs.

We help our customers produce safer, more sustainable food through supply chain and farm management software that delivers insights, drives better decisions and enables collaboration across global supply chains. Modernize your quality management by capturing product quality, process, facility and safety checks into a cloud-based solution. Providing a secure and easily accessed location for all your due diligence and quality data capture. Digitize every step of your product quality journey from raw material to end product. Incorporate third-party data sets and overlay A. I principles to optimize and steer inspection resources, improving utilization. Ensure the accuracy of labels through automated template recognition eliminating product recalls. Identify key risks and highlight required action to improve customer satisfaction, improve shelf-life performance and drive out waste. Centrally build quality attributes you wish to measure.

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

Effivity is a cloud-based / on-premise QHSE/FSMS/ISMS software to implement a robust Quality - Occupational Health & Safety - Environment Management System & offers 100% conformity to ISO 9001, ISO 14001, ISO 45001, ISO 22000, HACCP standards. Effivity makes ISO compliance simple, easy, quick, value adding, cost-effective, collaborative and time-saving which results in enabling an organization to enhance efficiency and augment productivity as validated by users in more than 120 countries. Effivity offers a unique approach to optimize your management system with world-renowned QMS software, HSE software & FSMS-HACCP software. Simplicity, standardization and customer satisfaction delivered with no-code quality management system software, safe workplace enabled with 100% customizable occupational health & safety management system, sustainable environment possible with a user-friendly environment management system and safe food delivered with HACCP software that is ready to use.

Software to conduct and automatically score assessments. The ERS Data System provides the information and tools that you need to conduct and accurately score assessments. Whether your focus is providing technical assistance or conducting high-stakes assessments, the ERS Data System can save you time and improve the quality of your assessment process. The ERS Data System is integrated with the most current notes for clarification directly from the authors, supplemental materials such as USDA meal guidelines, playground safety standards, and best practice information (handwashing, sanitizing, diapering procedures). The assessor’s handwritten notes are captured in worksheets, collecting information that is necessary to properly score each item. Justification notes at the indicator level, handwritten during the assessment, are then converted into text for reporting. Reports can be created at the classroom, facility, and organization levels.

CSols AqcTools™ v2.6 allows users to dynamically display Analytical Quality Control (AQC) charts to monitor lab performance, provides paper-free, auditable investigations of control limit failures, includes comprehensive reports and reduces the time to assess and process your QC data. Customers in water, environmental, public health sector and industrial laboratories undertaking chemical, clinical and microbiological analysis will benefit from AqcTools. It provides a selection of ‘dynamic, interactive’ charts from the standard ‘individual plotted AQC points’ to charts that can use batch or daily means of data, for both current and historic data. In addition, users can plot charts for an individual analyst to support the labs on-going analyst competency checking. All of the information relating to each individual point such as date, batch number, analyst, instrument etc. is just one mouse click away.

We have developed simple and effective tools to manage your EDM but also the validation cycle of your documents. Track your workflow accurately through clear dashboards, personalized forms and real-time indicators. Manage efficiently your workflow with Qualios with two perfectly integrated tools to efficiently facilitate the management of your information system. Because guaranteeing up-to-date and easily trackable information is essential, our Qualios Doc solution allows you to control your documents and their evolution. Qualios Manager adapts to your own quality indicators! Generate clear and concise forms and dashboards to quickly manage your internal workflow. Your improvement process requires a rapid control of all your flows. Qualios has been designed to facilitate your quality commitment and enable you to comply with ISO 9001, ISO 14001 or 18001 standards. These improvement processes should not become tedious or time-consuming