Alternatives to LINK Services

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.

Adaptive Compliance Engine® (ACE®) is a highly configurable, workflow based eQMS/eDMS and more that can adapt to any business process, allowing for real-time tracking, management, and reporting of all compliance, quality, and operational activities. With ACE®, you will minimize the administrative hassles and maximize ROI with productivity gains from day one – all while 21 CFR Part 11 compliant. Our one-stop software includes: -Office 365 Integration -Inspection Management -Document Management -Risk Management -Product Lifecycle Management -Learning Management -Audit Management -Quality Events -Paperless Validation -Electronic Signatures (21 CFR Part 11 Compliant) -Endless Workflow Configurations -And so much more! Empower all levels of your organization with intuitive user interfaces, easily search for all your documents and records, and transform your data into actionable intelligence with advanced analytics all on a single platform. ACE comes with everything you need, all included at one price. Every application is included, no more a la carte pricing. No more nickel and diming. One software, endless solutions.

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.

Certainty is an enterprise-level auditing and inspection software that can be trusted to help you manage and report on business risk, compliance, and performance metrics quickly and efficiently. Certainty Software is used by hundreds of thousands of professionals to complete millions of inspections and audits each year. It provides all the tools you need to collect, collate, and report consistent, accurate, and meaningful metrics across your business. Certainty provides all the tools you need to design, manage, and report on audit/inspection data, as well as help you manage and mitigate any risks, incidents, and issues that may be identified during the audit/inspection process.

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

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.

KPA is a leader in EHS Risk Management, Workforce Management and F&I solutions. KPA's innovative software platform, combined with recurring audit/loss control services, provides the visibility and actionable insights necessary for companies to prevent compliance-related, regulatory, and operational risks. KPA can help you achieve regulatory compliance, manage risk, protect assets, train, retain, and manage employees.

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

Companies today struggle to compile supply chain information for different products in today's fast-paced environment. This results in inconsistent data being scattered across multiple places, which can lead to inefficiencies in reporting supply-chain issues. Our digital solutions are designed to help you manage your business. UL's SmartSuite solution, PATH™, provides customized visibility into data reporting within one easy-to use platform. UL's SmartSuite (PATH™, SmartSuite) is a web-based platform that provides a single view of multiple tools and resources supporting Lifecycle Management and Information Management. These tools can help you save time, money, and reduce risk.

Failure Reporting Analysis and Corrective Action System is a closed feedback loop in which both the user and supplier work together to collect and record failures of hardware and software data. Corrective action (CAR) is greatest during design evolution. As a design becomes more solid, the implementation becomes more expensive and limited. The analysis will identify corrective actions to be implemented and checked in order to prevent failures from occurring again. FRACAS encourages reliability improvement during the entire life cycle of equipment. The method can be used during in-house (laboratory) tests, field (alpha or beta site) tests, and production/operations to determine where problems are concentrated within the design of the equipment.

Use accurate materials data from suppliers to generate compliance and sustainability reports. Be ready for changing global regulations. Full material disclosure improves product transparency. Manage your circular products for takeback and end of life. Transform supply chain complexity into customer-ready communications. Toxnot's supplier network can be used to search for or request data about your products. Integrate supply chain data easily to analyze your product portfolio. Respond quickly and efficiently to customer data requests. All your supply chain data can be easily integrated and managed across all products in your company. Reduce time spent managing product compliance. Visualize data and create any regulations that you need to manage your products. Toxnot allows you to connect all of your product compliance data across the supply chain.

Cloud software for the consumer goods industry and their supply chain. Solutions for material testing, collaboration, compliance, and material development. Texbase Testing reduces data entry time and costs. This helps to avoid costly delays in development. Texbase is one place for all your testing data. This includes your internal lab, all your suppliers, as well as independent testing labs. Power users can create new test methods and define data definitions themselves without the assistance of IT or consultants. You can either use the built-in protocols, or create your own. It produces consistent, accurate data quickly. It doesn't matter where it came from or what its purpose is. Integrated fiber, yarn and fabric libraries, as well as component libraries, provide the tools to create digital libraries and manage iterative development to speed innovation and decrease time to market.

A PDF report automatically generated from the data you provide. It covers product safety requirements, labeling and certification, as well as lab testing rules. A platform that helps manufacturers, importers, and brands find information about compliance requirements, book laboratory testing, create certificates, and label files. Third-party lab testing can be required when you import or manufacture products. It is usually necessary to prove that your product is safe. The lab test is used to verify that the product is compliant and safe. A lab test can be used to determine if a product contains harmful or restricted chemicals, such as phthalates. Lab testing can also be used to check for mechanical safety such as sharp edges and small parts.

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.

Clever Compliance (formerly CE Check) is a platform that offers a better way to manage global product compliance. Facilitate collaboration between departments and streamline compliance work in-house! CE Check was rebranded Clever Compliance in April 2020. It became a global product compliance platform. The CE marking software is no more available for subscription. Simply put, CE marking is a mandatory safety symbol that is placed on certain products sold in the EU/EEA. If this is your case, you will most likely be required to CE mark the product. To affix the marking to your product, you must pass the CE certification process. The service currently covers most of the CE marking directives as well as many of the main non CE directives. The service's scope continues to be expanded and new features, directives, and services are added.

Assent continuously maps complex manufacturing supply chains including aerospace, defense, electronics, industrial equipment, medical devices, and electronic components. We monitor suppliers, products, and parts to ensure your products are compliant and safe. Only Assent maps the entire manufacturing chain to unlock true sustainability. Your company will have unrivalled access to suppliers, parts, and products -- right down to the atomic level. This will allow you to lead, grow and win. Get an enterprise-wide view on sustainability, identify and prioritize key issues, keep up with changing regulations with automatic updates, plus much more. Assent helps you uncover the truth, validate what's good and eliminates any surprises. Assent assists the most sustainable manufacturers around the world by providing solutions that range from product compliance to ESG.

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.

We offer the most comprehensive and accurate coverage of key safety, environmental, and health regulations wherever you are. With solutions designed with the future of the world in mind, you can optimize your EHS compliance management. Compliance is more than just a concept. We can help you make compliance a reality by providing clear, actionable insights as well as expert guidance to ensure that you understand all aspects of EHS compliance and how to meet them. A more comprehensive compliance outlook can help you protect your business. To prepare for future policies, emerging issues, and other EHS trends around the world, look beyond legislation. Our in-house analysts are able to provide guidance and summaries that make it easy to understand the requirements, requirements, and insights. This will help you avoid costly fines and other setbacks. Increase collaboration, streamline screening, identify blind-spots across sites that share common ground in easy to navigate content - standardised across the globe and trusted and respected by the EHS community.

Relyence®, Failure Reporting Analysis and Corrective Action System, provides a complete framework for tracking and controlling all your concerns. Relyence FRACAS was designed and built for your specific needs, whether you are tracking customer complaints, field reports, test failures or safety concerns, or audit report findings. Relyence FRACAS reliability was built and designed with the understanding that no two corrective actions are the same. You need FRACAS software that is tailored to your specific needs and not vice versa. Relyence FRACAS offers a solution - you can use one of the built-in templates for 8D, DMAIC or PDCA, customize a template or create your own using our intuitive, easy to use customization features.

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.

Comply Express SmartCertTM, a revolutionary online product compliance management software tool, is designed to simplify and speed up product certification. The software tool is easy to use and can be configured to meet specific customer needs by entering product information from the relevant market sector. Comply Express was chosen for a reason. Our mission is to speed up new product certification processes in order to get new product designs to market as quickly as possible. Once products are on the market, we reduce the time and effort required to ensure compliance with legal requirements. SmartArt monitors product legislation to determine how your product portfolio relates to product safety standards. It will notify you if any products of yours may be affected by changes in the relevant standards.

Product Comply provides 360-degree monitoring of the evolving regulations and standards that impact your products. Our software can be customized to suit any compliance landscape, whether it's electronic products, medical devices, furniture, cosmetics, or any other product. Our product compliance software is able to navigate all global regulations related to any subject related to safety, health, and the environment. The regulations are then mapped to your product portfolio based on components, materials, or chemicals to ensure you stay ahead of any regulatory changes that could impact your business. Advanced software that monitors regulatory changes is essential to ensure your business is protected.

We are a technology and regulatory consulting company that assists businesses in implementing international standards, streamlining business processes, and accelerating global growth. Our in-house ISO consultants are available to provide expert guidance for your management system requirements. Our advisory services have been successful for many clients due to our international experience and our knowledge of companies that deal with software and hardware products in nature. No matter if you are a startup or an established company, you will find valuable features that can be tailored to your business, including setting up your QMS with all the necessary documents and maintaining it through proper document version control.

Screen formulations for product development and sourcing. To identify potential problems and find safer alternatives, use our 23 toxicological endpoints system. Know your company's chemical footprint. Automated management of compliance and certification requirements. A simple interface simplifies data collection, list screening, and chemical hazards assessments. The world's largest Safer Chemistry Knowledge Base contains more than 4,000 Verified chemical Hazard Assessments from Scivera toxicologists. You can create a plan that suits your budget and needs. You can submit or receive chemical reports with redacted information, regardless of whether you are a supplier or brand. This protects intellectual property and provides necessary chemical safety information.

What is QMS Audit Pro? QMS Audit Pro is an online platform for issue capture, auditing and corrective actions that is used over 15,000 times per month. QMS Audit Pro allows your team to collect consistent data, standardize operations and send reports. It also helps you identify problems and resolve them. It's also completely free. There are no contracts or commitments. You can cancel at any time. You can create Audit Plans, conduct Audits, monitor non-conformances, and track them all within one tool, achieving End-to-End traceability. Create company-wide audit and checklist templates that can be reused when performing audits. Make an audit report that includes pertinent information, such as audit summary, nonconformances and audit participants. This report can be customized to meet the needs of your company. You can quickly and confidently take action by linking data sources from various modules into powerful dashboards.

FavoWeb is the ultimate web-based FRACAS solution (Failure Analysis, Reporting, and Corrective Action). This comprehensive application allows unlimited user access through a single server or cloud-based SaaS. FavoWeb is easily configurable to match your workflow. It supports tailored data collection procedures and work processes. It also offers specific reports and statistical analysis. FavoWeb is the most advanced and leading software tool on the market for FRACAS. It will help you improve your failure analysis and corrective actions processes.

Corrective Action Workflow. Create actions. From any device, team leaders and internal auditors are able to create and assign corrective actions tasks. The new task is immediately notified to the team. Teams are kept informed by automatic notifications about changes in task stages and approval status. Teams can keep their leaders informed with dashboards, query filters, and costume searches. Teams can use permission-based approval-gates to ensure that tasks are properly investigated, corrected, and verified before closing the task. What is CorrectTrack? CorrectTrack is a workflow that allows you to control the entire corrective actions process. CorrectTrack allows you to: Assign corrective actions team members. To manage the process, create permission-based workflows. Team members and leaders can be informed about the status of tasks. To quickly see performance, create dashboards. Keep records and create reports about who did what and when.

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

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

Audit Manager is a software that supports quality management. It allows digital management of audits and quality controls in all phases: planning, compilation, and collection of evidence through checklists; verification and management for the entire nonconformity process; definition of corrective measures and data monitoring. You can access the calendar to schedule audits and add the relevant information (subject, checklists, lead auditor, coauditor or participants) for each one. Staff, both internal and outside, can be invited via email to consult the audit schedule prepared directly from the app. Once the inspection has been completed, you can generate the audit report as a PDF or Excel file and share it with the Company Management. You can add the archived minutes to the company's document repository.

A solid corrective action plan is essential to help your employees become the best they can. Organizations today are facing problems with inconsistencies, lack of oversight, and organizational disconnect when it is time to manage employee corrective actions. The PCA software solves these problems so that your Team can concentrate on improving culture, team building and efficiencies, as well as cost effectiveness. The PCA Solution can be customized to meet the needs of your organization. Super Users within your company will be able create flows and route. PCA integrates easily with your HR systems such as SAP, PeopleSoft and Workforce. The integration is a one way transmission of data that keeps your HR systems secure. PCA integrates company policies, procedures, and SOPs. In a central automated application that focuses on the issue and not the process.

Use the BOMcheck tools to keep up-to-date on new substance regulations and respond quickly to customer inquiries. A centralized blockchain database makes it easier for suppliers to keep current with all the latest substance regulations. Suppliers can securely manage their data in the database and download declarations in IPC 1752A XML or IPC 1752B XML. The Manufacturer Account is available for free if your company agrees that you pilot BOMcheck with a small number of suppliers. After the pilot is completed to your satisfaction, you can then request that your suppliers join BOMcheck at your discretion.

SansWrite, a cloud-based compliance monitoring platform, automates inspections. It also provides access to compliance data for trend analysis. SansWrite assists licensees in achieving and maintaining compliance and informs the community about the care of their loved ones. Visit www.sanswrite.com for more information.

MANUFACTURO is a dynamic, cloud-based software solution designed for the modern high-change manufacturing industry.

Customers, shareholders, NGO's, and market surveillance authorities are challenging companies involved in retail and trade about product issues. Every day, there are concerns about the safety of products. There are substances that are restricted and energy consumption that is not consistent with regulations. Products are becoming more complex as a result of the increasing number of technologies and regulatory agendas. This can hinder your growth and reduce your bottom-line. These are the aspects of businesses that management must control. ProductIP is a Compliance Tracking System, (CTS), that facilitates this. We transform complex regulatory information into a step by step approach that starts with something you will understand: a product. This will allow you to know what questions to ask suppliers and what documents they need to upload in a structured manner instead of sharing it in uncontrolled e-mails.

It is a constant challenge to maintain compliance standards for Substance of Very High Concern for chemical-containing products and companies that produce chemicals. Manual processes are becoming more complex and time-consuming due to growing requirements and an evolving supply chain. They can also be difficult to scale up. Manage peak loads during submissions or new product introductions. With constant follow-up from suppliers, managing large and complex supply chains. APA Engineering has over 19 years of experience in product chemical compliance. This web-based SaaS platform was built by APA Engineering to reduce costs and time, and provide comprehensive compliance reporting. Greencheck software automates the majority of the product chemical compliances. All it takes to get the chemical composition is a simple email Vendors can upload directly via excel. Comprehensive compliance reporting, one dashboard for all product chemical regulations.

In-app IMAP email, collaboration tools, and customer communication tools improve your communication with suppliers, customers, and team members. This simplifies coordination with all compliance stakeholders. Rumzerbot handles regulatory updates so that you can concentrate on your business. All plans include updates to regulations and declarable substances. Rumzer allows you to improve your supply chain communication and compliance process. Rumzer is not a middleman - we are your compliance software solution. All your compliance emails can be managed from one place. It's as simple as setting up an email account on your mobile device. Simply enter your email credentials, and you're done. You can add or remove users as many times as you like. To help you with compliance, you can add third-party service providers to your company.

Clearity.io, a security compliance management app, allows covered entities, business associates and their partners to measure their security program. They can conduct self-assessments and manage corrective actions plans. Our dashboard also displays real-time data. Do you have a lot of paper-based reports that provide information about your compliance and risk? How much time do your spend manually creating spreadsheets or combing through PDFs from third-party vendors? This is your organization. It's time for automation. Clearity allows you to feel in control over your security risks and know what needs to be done. Visually, your risks will decrease as you go along this path. You can create your own HIPAA, HIPAA (Vendors), CSC, NIST CSF, or NIST 800-53 Security Assessments. You can work on them at your own pace.

The Activator Approach is our three-stage methodology for delivering sustainable results. The Activator Approach is flexible enough to combine the right tools and expertise with a proven logic of change. The Analytics phase provides insight into business and sustainability issues, builds engagement and identifies risks and opportunities. Our methods include primary research, data collection, scenario modeling, big data analytics, and qualitative multi-stakeholder research. Global sustainability consultancy that drives performance across seven integrated service areas and creates value and positive change in all clients' lives.

iPoint places the needs of our customers at the forefront in all our actions and decisions. Our goal is to give you a competitive edge in today's dynamic and complex market. We have therefore consolidated our product portfolio into one suite, the iPoint Suite. The iPoint Suite provides solutions for all phases of the product life cycle, from design to production to use and recycling. We are the best partner to fully digitalize sustainable product life cycles and ensure compliance. Your data can be used to automate, streamline and digitalize your processes. Your supply chain resilience and social, economic, and environmental impact can be improved by knowing your data. Integrate the iPoint suite into your existing IT infrastructure to manage data across your entire company.

Our intuitive web-based interface allows you to search and find your requirements based on your Country, Wireless Technology, or Product. Data is organized in categories like Safety, EMC and Energy. So you can quickly find what your need. Read our News articles to stay informed about changes in requirements and how they could affect you. UL Go can provide you with examples of products such as laundry, kitchen, personal care, lighting, HVAC equipment, portable electronics and wireless technologies like WiFi, Bluetooth, 4G and other global markets. Contact us for a complete list. We review all requirements on a quarterly basis and update the requirements as soon we discover them. This ensures that the data is accurate and reliable.

Chemical Watch is the world's leading provider of independent intelligence and insights for chemical safety professionals. Chemical Watch is the most trusted partner to a global network of businesses, regulators, and other stakeholders. Join the Chemical Watch community today and empower your business. Comprehensive structured product compliance data solution that covers product regulations across all jurisdictions. This includes expert analysis and summaries. Participate in interactive question-and-answer sessions, 'ask an expert' themed networking tables, and informative presentations all from the comfort of home or work. You can network with conference speakers and fellow delegates in our virtual networking areas, just as you would at a live event.

Engage users from the front line to the C-suite with our configurable solutions--purpose-built with best-practice-based workflows and features--and embedded with AI, analytics, and mobile technology to quickly enhance performance at every stage of your digital transformation. Proven, flexible and powerful. Ready to deploy in three months or less. Organically built with, by, and for functional leader like you. Integrate with enterprise systems to deliver a superior user experience. Extend best-practice workflows, a versionless platform, and powerful pre-built configuration options with quick-to launch. Engage, communicate and drive key stakeholder performances via the industry's robust, integrated Mobile & Analytics platform.

Software solutions that make organizations more resilient and sustainable are what we create. Our innovative technology can make your organization more efficient, resilient, sustainable, and better for the world. Our software solutions enable companies to manage safety and environment performance, ensure compliance and minimize risks, improve profitability, and leverage some of the most advanced technologies in the world. Our H&S management software will ensure the safety and health of your employees, assets, and the community. Our solutions cover all aspects of worker safety and health as well as process safety management. They help you prevent and predict incidents, keeping your employees healthy and productive. Ensure your business operations are reliable and efficient, as well as maintaining the productivity of your employees. Recognize and mitigate potential risks to production and manufacturing targets.

To produce high-quality, profitable food products, the food manufacturing business needs buyers, technical, quality, and production staff to work together. 3iVerify, a cloud-based, affordable food safety management system, helps technical, quality, and compliance managers manage the tidal wave process, procedures, and paperwork they deal with every day. This is achieved by using a simple and logical approach to key processes such as supplier and material approvals management, supplier monitoring and document management and corrective actions management. We believe life is too short to be surrounded by spreadsheets and paperwork. We work closely with our customers to ensure that their system is tailored to their business model. We can only offer you the modules that you need so you don't have to spend money on things you won't use. Visit our website to learn more about the solutions we offer.

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.

We invented the market for compliance and quality digitization. We are constantly improving our solution with innovative business & artificial intelligence technologies. Our success is the success of our clients! Our team will work closely with you every step of the way to get you there. Pivot88, a cloud-based software that integrates all data, in real time, allows 360deg supply chain transparency, for brands, suppliers, factories, and retailers. Integration with all business systems (ERP and PLM) and data sources (lab tests, documents and eLearning materials, among others) is possible. Our system instantly captures data and transforms it into actionable, real time analytics. We also offer a variety of reporting tools that will help you make better and faster decisions. Our solution is the first to incorporate Applied Artificial Intelligence, which helps your teams to predict and manage future risk.

Food Safety Software allows for cost-effective transformation in food safety, NPD and customer complaints, as well as supply chain transparency. Our food safety software includes VACCP/TACCP and horizon scanning to help you save time and complete consistent, auditable risk assessment of suppliers and products. You will never be audited in non-conformance and you can be audit-ready 24 hours a day. Transform specification management for raw materials and finished products, and answer customer queries instantly. Automate supplier quality monitoring and internal non-conformance management using automated workflows. This will ensure that non-conformances are promptly closed. Our team will manage all complaints using market-leading software. This will save you time, money, and improve customer service. You can launch new products faster and better together, while still meeting all safety, legality, and profitability requirements.

The Intact Platform, a cloud-based and on-premise Enterprise Resource Planning solution (ERP), is the best for audits, assessments certification, accreditation, and other standards. It is more than any other audit collection tool on the market. It offers a complete solution that helps you manage communications and business goals as well as personnel. Intact Platform is unrivaled in functionality and features an end-to-end modular workflow that is easily scaleable. 34% efficiency increase on average (upto 60+%) Unmatched modularity, flexibility and scalability All standards and audit services Digital workflow - no need for paper Remote and on-site auditing Non-conformities and corrective actions Planning and risk-based auditing Communication with clients is easy Reporting and business intelligence (BI). Management and central data hub (incl. Audit trail complete Innovation never stops