LINK Services Alternatives

Intelex is an integrated software solution for managing Environmental, Health, Safety and Quality (EHSQ) programs. Intelex’s scalable platform is designed to store, manage and analyze EHS and Quality data in one place. The solution works on any device to meet the realities of your workplace. With Intelex, your organization can: - Drive better results in your EHSQ program by monitoring workflows to achieve top performance and gain control. - Identify trends and tendencies by setting goals to gain greater insight into your EHSQ program to enhance judgement. - Reduce incidents and administrative work by easily monitoring, managing, optimizing and drawing insights from your safety data with our user-friendly safety software solution. - Streamline air, water and waste emissions management and reporting, and track and manage environmental outputs to achieve sustainability goals. - Drive continuous quality improvement activities across multiple departments, sites or locations.

ReliaSoft software provides a powerful range of reliability software solutions to facilitate a comprehensive set of reliability engineering modeling and analysis techniques. We are the leading reliability solution provider for product test, design, maintenance strategy and optimization. Our products support a wide range of reliability and maintainability analysis techniques, such as life data analysis, accelerated life testing, system modelling and RAM analysis, reliability growth, FRACAS, FMEA and RCM analysis to meet and improve reliability of your products, processes and optimize maintenance planning.

isoTracker Quality Management is a popular cloud-based quality management software (QMS) that is used by small to medium sized businesses on a worldwide basis. It helps to manage ISO 9001, ISO 13485, ISO 22000, ISO/IEC 17025, ISO 14001, ISO 45001, ISO/TS 16949, ISO 14971 systems...plus many other systems. It also conforms to the requirements of 21 CFR Part 11. It is a flexible and modular product with modules in document control, audit management, non-conformance management, customer complaints management, risk management, training management and CAPA management. It can be configured to meet an organization's specific needs and provides free training and free support. It has been independently judged to provide the best customer support in its category.

ACE is a quality management software solution for companies of any size, in any stage, in any highly regulated industry. ACE is fully configurable allowing your company to adapt ACE to fit into your exact quality needs. 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. 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! 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. Artintech ERP includes a wide range of modules designed to optimize business operations. Key modules include Procurement, Warehousing, CRM, Distribution, Quality Management (QMS), Workplace Safety, Document Control, Non-Conformance and Corrective and Preventive Actions (CAPA), Inspection, and Computerized Maintenance Management System (CMMS).

Improve Performance and Sustainability with Certainty! Certainty is an enterprise-level software solution to easily collect and report inspection data and manage issues identified. Used by hundreds of thousands of professionals to complete millions of audits and inspections annually, Certainty helps companies around the globe ensure compliance, reduce risk, and improve performance with easy-to-use forms, real-time reports, and complete action management. Collect, track, and report accurate and powerful data to provide detailed business insights that will empower your team to improve performance and business sustainability. Certainty is used worldwide for: Safety inspections Quality assurance and control audits Supplier and supply chain compliance audits ESG assessments And much more . . .

SimplerQMS offers a cloud-based Quality Management Software that is fully validated according to GAMP5 and specifically designed for the Life Science industry. This comprehensive QMS platform 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, ICH Q10, and others. The software offers a wide range of Life Science QMS modules, such as Document Control, Change Management, Training Management, Supplier Management, Complaints Management, Non-Conformance and Deviation Management, CAPA Management, Audit Management, Technical Documentation Management, Risk Management, Quality KPIs, among others, ensuring a seamless experience. SimplerQMS enhances document handling by allowing users to work directly in Microsoft Office applications like Word, PowerPoint, and Excel.

QT9's comprehensive cloud-based quality management software platform enables you to access real-time analytics in one unified suite. QT9 QMS makes it easy to automate ISO & FDA Compliance with 21 CFR Part 11 Electronic Approvals. Optimize processes for Document Control, CAPA's, Audits & More in one unified platform. Centralize records across multiple sites with ease. Never miss a deadline with automated email alerts/reminders. QT9 QMS makes quality management easy. Digitally transform Life Sciences, Biotechnology, Medical Device Manufacturers, Pharma, Aerospace and Food companies with user-friendly web portals for unlimited scalability. Get a free product tour! Start a Free Trial. Visit QT9qms.com

Qualio is an all-in-one quality and compliance management platform built for small and growing businesses in life sciences and healthcare. Reliable, affordable, and easy to use, Qualio helps companies building life saving products get to market faster by reaching 100% ISO, GxP, and FDA compliance. With Qualio, companies can conveniently manage document control, training, CAPAs, NCRs, audits, suppliers, complaints, and more in one platform.

KPA is a leading provider of EHS Risk Management, Workforce Management, and F&I solutions. KPA’s innovative software platform combined with recurring on-site audit/loss control services delivers the visibility and actionable insight necessary for companies to proactively mitigate operational, regulatory, and compliance-related risks. KPA helps you achieve regulatory compliance, control risk, protect assets, and effectively train, retain, and manage people. Introducing an EHS software platform tailored to the needs of your business. Manage your safety program in an all-in-one system designed to engage your employees, instill a culture of safety, and enable regulatory compliance. KPA EHS helps you develop a comprehensive EHS program that harnesses technology, best practices, and the concerted efforts of your workforce to maintain a safe and productive workplace. Use KPA’s mobile technology to access the tools and information you need, where you need it.

Failure Reporting, Analysis, and Corrective Action System (FRACAS) is a closed-loop feedback path in which the user and the supplier work together to collect, record, and analyze failures of both hardware and software data sets. Corrective action (CAR) is greatest during design evolution. It becomes more limited and expensive to implement as a design becomes firm. The resulting analysis identifies corrective actions that should be implemented and verified to prevent failures from recurring. FRACAS promotes reliability improvement throughout the life cycle of the 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.

In today’s fast-paced world, companies struggle to collect and compile supply chain data in one place for various products. This leads to inconsistent data being scattered across multiple locations causing inefficiencies in reporting supply chain issues. Our comprehensive suite of digital solutions is designed around managing your business. UL’s PATH™ SmartSuite solution provides customized visibility into data reporting in one easy-to-use platform. UL’s PATH™ SmartSuite is a web-based platform providing a single unified view of various tools and resources supporting Lifecycle Management, Information Management, Business Intelligence, Corrective Action, and Technical Questions. These tools can save you time, money and risk.

Cloud software for the consumer products industry and their supply chains. Solutions for material development, testing, color, compliance and collaboration. Texbase Testing reduces data entry costs, improves accuracy and timeliness of information preventing costly development delays. Texbase provides one location for all your testing data and documents. This includes your internal lab (if you have one), all your suppliers, and independent testing labs. Power users can easily create new test methods and define their data definitions without the help of Texbase, IT or consultants. Use the built-in protocols or define your own. The result is consistent and accurate data, fast. Regardless of where it's coming from or its purpose. Integrated fiber, yarn, fabric, and component libraries provide the tools you need to build digital libraries and manage the iterative development process to accelerate innovation while decreasing time to market.

Generate compliance & sustainability reports using accurate materials data maintained by suppliers. Be prepared for unpredictable evolving global regulations. Improve product transparency with full material disclosure. Manage your circular products for end of life & takeback. Turn supply chain complexity into customer ready communications. Leverage Toxnot's supplier ecosystem to find or request data of your products. Easily integrate supply chain data to analyze your product portfolio. Quickly and efficiently respond to customer data requests. Easily integrate & manage all your supply chain data across every product in your company. Save time spent on managing your product compliance. Visualize data and configure any regulations you need when managing your products. With Toxnot you're able to unify all your product compliance data across your supply chain on one platform.

Empower your business with actionable and measurable results and gain a comprehensive view of ESG performance and risk in real time. For generations, companies found it near-impossible to generate a holistic view of their risk profiles. Today, they have SpheraCloud®, an integrated ESG performance and risk management software platform. SpheraCloud is a key part of Sphera’s approach to addressing safety and sustainability issues before they even occur. It allows users to not only get the right information to the right people at the right time, but also empowers them to make better business decisions with its predictive and prescriptive capabilities. Many companies struggle to connect disparate data throughout their organizations and their value chains, and to communicate that risk efficiently and effectively. It’s hard to complete such an enormous task—without SpheraCloud. The innovative SaaS platform empowers your company to gain a comprehensive view of ESG performance and risk.

Create an automatically generated PDF report covering product safety requirements, labeling, certification, and lab testing rules for a wide range of products in the EU and the United States. An online platform helping brands, importers and manufacturers find information about compliance requirements, book lab testing, create certificate, and label files. Third-party lab testing is often mandatory when importing or manufacturing products – or at least necessary for the sake of demonstrating that your product is safe and compliant. The purpose of the lab test is to determine if the product is safe and compliant. For example, a lab test can determine if a certain product contains harmful and restricted chemicals – such as phthalates. Lab testing can also cover mechanical safety, such as sharp points and small parts.

The Assent platform continuously deep-maps complex manufacturing supply chains, including aerospace & defense, automotive, electronics, industrial equipment, and medical devices. From product compliance to ESG, we monitor suppliers, products and parts so you know your products are safe, compliant, and sustainable. Only Assent works to map the entire manufacturing genome to unlock true supply chain sustainability. Unmatched access to suppliers, products, and parts — down to the atomic level — puts your company in a position to lead, grow, and win. Unlock an enterprise-wide view of sustainability, identify and prioritize critical issues, stay ahead of changing regulations with automatic updates, and so much more. Assent reveals what’s hidden, validates what’s good, and helps eliminate unwanted surprises. With solutions from product compliance to ESG, Assent helps the world’s most sustainable manufacturers win.

IQE is MediaLab’s non-conforming event management system that allows clinical laboratory teams to track, assess, and prevent non-conforming events (NCE). With the capability to import or create event forms and data logs, IQE enables laboratory teams to eliminate deficiencies, correct common NCEs, and, most importantly, focus on improving healthcare. With a MediaLab institutional subscription, administrators can easily document each phase of the event management lifecycle, from initial event description to risk analysis, investigation, and root cause analysis, corrective and preventive actions plans, and overall CAPA effectiveness evaluations. IQE supports: • Customizable, pre-built event forms and workflow • Monitoring and evaluating change control events, failed PT events, customer complaints / feedback, safety / injury events, supplier / vendor issues, and more • Tracking periodic data entries • Robust reporting and dashboards to identify common NCEs and CAPA effectiveness

A web-based quality system software suite that helps medical device companies automate their processes and simplify regulatory compliance. Modules include: Audit Management, CAPA, Complaint Handling, Design Control, Document Control, Equipment Management, Nonconforming Materials Reporting, Supplier Management and Training Management. Designed from the beginning for ISO 13485 and 21 CFR Part 11 compliance. Audit results are recorded for each requirement in the audit. Requirements are marked as conforming, nonconforming, or not applicable. Each result may be detailed with one or more findings. Findings that may be recorded include observations, major nonconformances, and/or minor nonconformances. Findings may result in Corrective and Preventive Actions (CAPA) and/or may be documents with audit actions already completed.

CE Check is now Clever Compliance, offering you a new, improved platform for global product compliance management. Streamline in-house compliance work and facilitate collaboration between departments! In April 2020, CE Check transformed itself into a global product compliance platform and rebranded as Clever Compliance. Thereby, the CE marking software is no longer available for subscribing. Simply, CE marking is a mandatory safety symbol placed on certain products being sold in the EU/EEA. If that’s your case, then you are most likely required to CE mark your product. However, to affix the marking on your product, you need to pass the CE certification process successfully. At the moment, the service covers the majority of CE marking directives and many of the main non-CE directives. The service’s scope is constantly being upgraded and new directives, features, and services added.

We provide the most complete and precise coverage of key environmental, health, and safety regulations wherever you operate. Optimize your EHS compliance management with solutions built with our world and its future in mind. Compliance is more than a concept. We help you make it reality with clear, actionable insights and expert guidance for a full understanding of EHS compliance requirements and how to achieve them. Protect your business with a more expansive compliance outlook. See beyond legislation to prepare for upcoming policies, arising issues, and other EHS trends worldwide. Avoid costly fines and damaging setbacks with easy-to-understand summaries, requirements, insights, and guidance from our knowledgeable in-house analysts. Increase collaboration, streamline screening, and identify blind-spots across sites with common ground in easy-to-navigate content – standardized across the globe and trusted by the EHS community.

Relyence® Failure Reporting, Analysis, and Corrective Action System software provides a complete tracking and control framework for the proper handling of all your issues of concern. Whether you want to track customer complaints, field failure reports, test failures, safety issues, compliance concerns, audit report findings, or any other type of incident, Relyence FRACAS is designed and built to meet your needs. Relyence FRACAS reliability software was designed and built with the knowledge that no two corrective action processes are the same. When looking for FRACAS software, you need a tool that can be tailored to your needs, and not vice-versa. Relyence FRACAS is the solution – use one of our built-in 8D, DMAIC, or PDCA templates, customize a template, or create your own with our intuitive, easy-to-use customization features.

Explore FavoWeb, the ultimate web-based FRACAS (Failure Reporting, Analysis, and Corrective Action) solution. This comprehensive application ensures unlimited user access via a single server installation or cloud-based SaaS solution. Easily configurable to align with your specific workflow, FavoWeb supports tailored data collection procedures, work processes, business rules, and offers specific reports and statistical analyses. Elevate your failure analysis and corrective action processes with FavoWeb – the market's leading and most advanced software tool for FRACAS.

QMS Audit Pro is an audit, issue capture and corrective action platform that's used over 15,000 times a month. QMS Audit Pro lets your team collect consistent data, standardize operations, send reports, identify failed areas and get problems resolved with this easy-to-use checklist audit platform. Best of all it's free. No contracts or commitment required. Cancel anytime. Create Audit Plans, conduct Audits, and monitor non-conformances within one tool and achieve End-to-End Traceability. Define company-wide audit and checklist templates which can be re-used when creating and performing audits. Create an audit report with pertinent audit information such as; audit summary, non-conformances, and audit participants. This report can be customized based on company's requirements. Take action quickly and confidently by linking data sources from different modules into powerful dashboards.

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.

Product Comply offers comprehensive 360-degree monitoring of evolving regulations and standards impacting your company’s products. Whether it’s medical device products, electronics, furniture, cosmetics or any other product – our software is customized around any compliance landscape. Our product compliance software successfully navigates all global regulations; related to any specific subject related to health, safety, and environment. Regulations are then mapped to your product portfolio according to components, materials, and chemicals to keep you ahead of any possible change in the regulatory scenario impacting your business. With consistently global evolving EHS (Environment, Health & Safety) regulations, laws, and compliance perimeters, it’s imperative to rely on advanced software that monitors regulatory changes to reduce monitoring efforts and to enable your team to focus on strategic decisions to protect your business.

Comply Express SmartCertTM is a game-changing new product compliance management online software tool designed to speed up and simplify the product certification process. The easy-to-use software tool is automatically configured to specific customer’s needs by entering product information for the relevant industry sector and target markets. We chose the company name Comply Express for a reason – our mission is to speed up the new product certification process in order to help get new product designs to market in the shortest possible time – and once on the market, reduce the time and minimize the effort required to keep products in compliance with legal requirements. SmartArt monitors product legislation and knows how product safety standards and other standards relate to your product portfolio. It will warn you if any of your products may be affected by up-coming changes in relevant standards.

Screen formulations for sourcing and product development. Use our 23 toxicological endpoint system to proactively identify potential issues and find safer alternatives. Understand your company’s chemical footprint. Manage compliance and certification requirements automatically. Simplify data gathering, list-screening, and chemical hazard assessments with an easy-to-understand interface. Benefit from the world’s largest Safer Chemistry Knowledge Base with more than 4,000 Verified Chemical Hazard Assessments from Scivera’s board-certified toxicologists. Build a configurable plan to fit your needs and budget. Whether you’re a supplier or a brand, feel confident submitting or receiving chemical reports with redacted information that protects intellectual property while providing necessary chemical safety information.

We are a regulatory consultancy and technology company that helps businesses implement international standards, streamline business processes across the organization, and accelerate global growth. Our team of in-house ISO consultants can provide trusted guidance towards your management systems requirements. Given our international expertise, besides experience with companies handling hardware and software products in nature, our advisory services have proven successful for a wide variety of clients. From setting up your QMS with a complete set of documents to maintaining your QMS through proper document version control and automated workflow processes, you will find valuable features tailored to your organization, regardless of whether you are a start-up or an established organization.

Corrective Action Workflow. Create Actions. Team leaders and internal auditors can create and assign corrective action tasks from any device. Team members are notified immediately of the new task. Teams stay informed with automated notifications of changes in task stage and approval status. Dashboards, query filters and costume searches helps teams keep leadership informed. Permission based approval-gates help teams ensure tasks are investigated, corrected and the corrective action is verified before the task is closed. What does CorrectTrack do? CorrectTrack is a workflow that gives control over the entire corrective action process. With CorrectTrack you can: Assign corrective actions to team members. Create permission-based workflows to control the process. Communicate task status to team members and leadership. Create dashboards to quickly view performance. Retain evidence and produce reports of who did what and when to investigate.

Audit Manager is the software supporting quality management that allows digital management of audits, quality controls and tests in all their phases: planning and compilation through checklists, collection of evidence and field surveys, verification and management of the entire nonconformity flow, definition of corrective actions and data monitoring. Access the calendar and schedule the audits by associating the relevant information with each one (subject, checklist, lead auditor, co-auditor, participants, etc.). The staff involved, both internal and external, can receive an invitation via email and consult the prepared audit schedule directly from the app. Once the inspection is completed, generate the audit report in PDF or Excel and share it directly from mobile with the company management or managers. The archive of all minutes is always available and organized and you can add it to the document repositories used by the company.

FactoryQA is an all-in-one Quality Management software for Manufacturers. Software Features: 1. Non-Conformance/CAPA Management 2. Document Control 3. Work Instructions 4. Inspection Sheets 5. Audits 6. Analytics Services: 1. ISO Certification Consultants 2. ISO Certification Workshops 3. Fractional Quality Management Services

Helping your employees be the best they can be requires a solid corrective action process to improve performance before things go wrong. Organizations are struggling today with inconsistent processes, lack of oversight and organizational disconnect when it comes to managing employee corrective actions. The PCA software solves all of these challenges so your Team can focus on advancing culture, team building, efficiencies and cost effectiveness. The PCA Solution is customizable for the organization's specific process flows and needs. Super Users within your organization will be able to define flows and routing. PCA easily integrates with your HR systems like SAP, PeopleSoft, Workforce, etc. The integration is a one-way transmission of data which keeps your HR systems secure. PCA integrates your company policies, procedures and SOPs. in a centralized automated application which returns the focus to the issue instead of the process.

MANUFACTURO is a dynamic, cloud-based software solution designed for the modern high-change manufacturing industry. By consolidating disparate systems into one cohesive platform, your organization is effortlessly streamlining operations, improving data accuracy, and enhancing operational efficiencies. Our key differentiators are your new competitive advantage. Traceability and nonconformance management are just two examples of industry-leading capabilities that showcase Manufacturo’s unique value. Cutting-edge traceability, powered by advanced monitoring technology, provides you with a holistic view of your manufacturing operations. From inspection of materials arriving at your facility to customer shipment, you’ll realize enhanced safety, compliance, and operational efficiency, driven by real-time situational awareness that’s available at your fingertips. Our built-in nonconformance management solution seamlessly integrates with your organization’s production, inventory

SansWrite is a cloud-based compliance monitoring platform that automates inspections and corrections, and provides access to compliance data for trend analysis and government transparency. In other words, SansWrite helps inspectors increase productivity, assists licensees with achieving and maintaining compliance, and informs communities about the care of loved ones. For more information, please visit www.sanswrite.com today.

Clearity.io is a security compliance management application that provides covered entities, business associates, and their partners the ability to measure their security program by conducting self-assessments, managing corrective action plans, and working towards industry-driven compliance while viewing real-time data on our dashboard. Does your risk and compliance intelligence come from pages and pages of paper-based reports? How much time do you spend manually creating or combing through spreadsheets and PDFs from 3rd party vendors? If this is your organization, it’s time to automate that process. Clearity gives you the ability to feel in control of your security risks and to know what work needs to be completed. As you head down that road, visually see your risks diminish over time. Create your own HIPAA, HIPAA (Vendors), CSC, NIST CSF, or NIST 800-53 Security Assessments. Work on them on your own time.

Cognidox is an online document management system for high-tech, medical device and life sciences product development sectors. Available in the cloud or as an on-premise solution, Cognidox promotes better product lifecycle management and knowledge transfer from developers to clients, partners, and customers. Secure and reliable, Cognidox provides plug-ins for various programs such as Microsoft Office, and we also offer a robust API so that you can integrate almost any process with Cognidox In addition to the core function as a DMS, an add-on for Cognidox also offers a way of allowing licensing and distribution of documents to third parties via fully sandboxed site so you have the power to publish specific documents whilst keeping your main storage secure. Another popular add-on is the gBMS - graphical Business Management System, Use Visio to easily capture your business processes, a good BMS should give you clear oversight of your entire operation.

Keep up-to-date with new substance regulations and respond to customer requests by using the BOMcheck tools to generate Regulatory Compliance Declarations (RCD) and/or Full Materials Declarations (FMD). Centralized blockchain database saves time and cost for suppliers to keep up-to-date with new substance regulations around the world. Suppliers can manage their data securely in the database and download declarations in industry standard IPC 1752A XML, IPC 1752B XML, PDF or Excel Formats. The Manufacturer Account is free-of-charge provided that your company agrees to pilot BOMcheck with a limited number of suppliers and, on successful completion of the pilot to your satisfaction, then request your suppliers to join BOMcheck, at your discretion.

Maintaining compliance standards for Substance of Very High Concern (SVHC) for companies producing chemicals or chemical-containing products is an ongoing challenge. Manual processes are fast becoming tedious, complex with growing requirements and evolving supply chain and not easy to scale up. Scale-up & manage peak loads during submissions and new product introductions. Managing complex and large supply chains with relentless follow-up with suppliers. APA Engineering with over 19+ experience in ‘product chemical compliance and a global client base has built this web-based SaaS platform to reduce costs & time and achieve comprehensive compliance reporting. Greencheck software automates most of the critical product chemical compliances. One-click email to get the chemical composition. Vendors can upload directly even via excel. Comprehensive compliance reporting, a single dashboard for all product chemical regulations.

Companies involved in retail and trade are increasingly being challenged by customers, shareholders, NGO's and market surveillance authorities about issues with products. Every day there are issues with the safety of products, with substances that are restricted, with energy consumption that is not in line with regulations. The regulatory agenda is becoming more and more complex and, because of adding more and more technologies, so are products. Not being able to cope with this is potentially hampering your growth and reducing bottom-line results. These are aspects of businesses that management needs to control. ProductIP is a Compliance Tracking System (CTS) that facilitates that. We convert complex regulatory information into a step-by-step approach that starts with what you will understand: a product. You will then know what questions to ask your suppliers, what documents they need to upload directly in a structured way instead of sharing this in an uncontrolled way via e-mails.

In-app IMAP email and collaboration tools improve your communication with customers, suppliers, and team members - simplifying coordination with all compliance stakeholders. Rumzerbot manages regulatory updates so you can focus on your business. All plans include updates to declarable substances and regulations. Rumzer enables you to better control your compliance process and supply chain communication. We're not a middle man - we're your compliance software solution. Manage compliance emails in one spot. Set-up is as easy as setting up email on your mobile device. Just enter your email credentials and go. You can add and remove users as you wish. You can even add 3rd party service providers to your organization to help with your compliance work.

We at iPoint put our customers’ requirements at the forefront of all our actions and decisions. Our goal is to provide you with a competitive advantage in today’s complex and dynamic market. Therefore, we have consolidated our product portfolio into a single suite – the iPoint Suite. The iPoint Suite offers you solutions for the entire product life cycle – from design to production and use to recycling and reuse. As the best partner for fully digitalized life cycles of compliant and truly sustainable products, we support you on your journey from compliance to sustainability – wherever you are. Automize, streamline, and digitalize your processes leveraging your data. Know your social, environmental, and economic impact and strengthen the resilience of your supply chain. Manage data across your entire organization by integrating the iPoint Suite into your existing IT landscape.

The Activator Approach is our three stage methodology for delivering sustainable performance. Whether corporate strategy or specific operational problem solving, the Activator Approach flexibly combines the right expertise and tools for the job, across a proven, end-to-end logic of change. The Analytics phase develops insightful diagnostics of business and sustainability issues, builds engagement, and identifies opportunities and risks. Our methods combine primary research and data collection, big data analytics, scenario modelling and multi-stakeholder qualitative research. Global sustainability consultancy, driving performance across seven integrated service areas, creating value and positive change for all clients.

Chemical Watch is the leading global provider of independent intelligence and insight for product safety professionals managing chemicals. Chemical Watch is the world’s most valued chemical safety and regulatory intelligence network and trusted partner to a global community of businesses, regulators and other stakeholders. Join the Chemical Watch community today to empower your business. Comprehensive structured product compliance data solution providing coverage of product regulations across all jurisdictions, including legal documentation, expert analysis and summaries. Attend our virtual conferences to take part in interactive question and answer sessions, ‘ask the expert’ themed networking tables and informative presentations, all from the comfort of your home or office. Network with fellow delegates and conference speakers in our dedicated virtual networking areas – just like you would at a live event.

Use our intuitive web-based interface to search and find requirements based on your Product, Wireless Technology, or Country. Data is organized into categories such as, Safety, EMC, Energy, etc. so you can quickly find what you need. Read News articles written by our experts to keep you up-to-date on changing requirements and how it could impact you. Examples of the type of products you can find in UL Go include: laundry, kitchen, and personal care appliances, lighting products, HVAC equipment, portable electronics, and wireless technologies such as WiFi, Bluetooth, and 4G, for markets all over the world. For a full detailed list, contact us to see how we can meet your specific needs. We update the requirements as soon as we find out and review all other requirements on a quarterly basis so you know the data is reliable and accurate.

We create software solutions that make organizations more sustainable. Create a better world by making your organization more efficient, resilient, and sustainable through our innovative technology. Our software solutions help companies manage safety and environmental performance, ensure compliance, minimize risks and improve profitability by leveraging some of the world’s most advanced technologies. Ensure the health and safety of your workers, assets and the wider community with our H&S management software. Covering all aspects of process safety management and worker safety and health, our solutions help you predict and prevent incidents – keeping your employees safe and fit for work, and making your workforce more productive. Ensure that business operations are reliable, efficient and maintain the productivity of your workforce. Identify and mitigate risks that can threaten production and manufacturing targets.

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 3 months or less. Organically built by, with, and for functional leaders like you. Realize superior user experience from the only seamlessly unified digital platform for EHS, Sustainability & ESG Reporting and allied functions; and integrate with enterprise systems. Extend out-of-the-box, best-practice workflows and a version-less platform with quick-to-launch, powerful pre-built configuration features and options for custom extensions. Engage, communicate & drive key stakeholder performance via the industry’s most robust, integrated Mobile and Analytics platform.

In a food manufacturing business, buyers, production, technical and quality staff all need to work as a TEAM to produce profitable, safe, and high quality food products. 3iVerify is an affordable, secure, cloud-based food safety management system that helps technical, quality and compliance managers tame the tidal wave of processes, procedures and paperwork that they deal with every day. We achieve this by having a simple, logical approach to key processes like supplier and material approvals management, supplier monitoring, document management and corrective action management. We believe that life is too short for spreadsheets and paperwork. We always work with our customers to ensure their system is bespoke and tailored to their specific business model. We can offer you only the modules you need, so you don't need to waste money on stuff you wont use. For further information please visit our website for a comprehensive introduction to the solution we offer.

Food Safety Software enabling cost-effective transformation of food safety, NPD, customer complaints and supply chain transparency. Save time and complete consistent, auditable risk assessments of products & suppliers; our food safety software includes horizon scanning and VACCP/TACCP. Be audit-ready 24/7 and never receive an audit non-conformance, guaranteed. Transform specification management for raw materials, and finished products and answer product queries instantly. Automate supplier quality monitoring or internal non-conformance management with automated workflows to ensure prompt closure of non-conformances. Let our team manage the entire complaints process using market-leading software to save time, money and improve customer service. Deliver new product launches faster, better, together while ensuring that all safety, quality, legality and profitability requirements are met.

We created the market of quality & compliance digitization and are continuously enhancing our solution through innovative business & artificial intelligence technologies. Our clients' success is our success! Our team is dedicated to working closely with you each step of the way to help get you there. Pivot88 is a cloud-based solution that integrates all data in one place, in real-time, enabling 360° supply chain transparency for brands, retailers, suppliers & factories. We provide full integration with all business systems (ERP, PLM) & data sources (lab tests, documents, eLearning material, and more). Our system instantly captures and translates data into actionable, real-time analytics with a variety of reporting tools to help you make smarter and faster decisions. We are the first to introduce Applied Artificial Intelligence to our solution, helping your teams predict and manage future risks.