Alternatives to Quality Control Platform

QRA’s tools streamline engineering artifact generation, evaluation, and prediction, refocusing engineers from tedious work to critical path development. Our solutions automate the creation of risk-free project artifacts for high-stakes engineering. Engineers often spend excessive time on the mundane task of refining requirements, with quality metrics varying across industries. QVscribe, QRA's flagship product, streamlines this by automatically consolidating these metrics and applying them to your documentation, identifying risks, errors, and ambiguities. This efficiency allows engineers to focus on more complex challenges. To further simplify requirement authoring, QRA introduced a pioneering five-point scoring system that instills confidence in engineers. A perfect score confirms accurate structure and phrasing, while lower scores prompt corrective guidance. This feature not only refines current requirements but also reduces common errors and enhances authoring skills over time.

ProShop is a web-based, paperless shop management, ERP, and MES system for manufacturing companies in regulated sectors. ProShop was built in a machine shop on the floor. It's unlike anything else you've ever seen. ProShop was designed to handle complex manufacturing environments better than any other product on the market. This system gives you unprecedented insight into every aspect of your manufacturing company. ProShop can be described as a Digital Manufacturing Ecosystem. It is 100% paperless and combines the features of ERP, MES and QMS with other software categories. This is for machine shops and fabricators, job shops and contract manufacturers, as well as others in regulated sectors who need tight control over their processes and need accurate and timely information to make the most profitable decisions.

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.

All-in-One LIMS, ELN, QMS, and DMS Platform Xybion LIMS is an all-inclusive Digital Laboratory system including LIMS, ELN, QMS, and DMS that creates optimized workflows for the unique business needs of all regulated laboratories including research, diagnostics, quality control, stability studies, and more. Xybion LIMS instills consistency, improves data quality, and supports regulatory compliance with a complete laboratory management solution that connects with your operating systems with powerful laboratory information management and analytics.

TLM QMS Software is a powerful and robust quality, risk and material management software (QMS) which is validated and 21 CFR Part 11 compliant. TLM is a cutting-edge, all-in-one quality management system that can be customized to integrate with online CRM software, QuickBooks or ERP databases. Total Lean Management (TLM) QMS Software is specifically intended to be a low cost, highly integrated, flexible and continuously improving landscape to which specialty systems can be added where needed to create the digital business landscape that enables work flows the way your company needs them to work.

Organizations need to standardize their business processes and automate them in order to bring new products to market quickly and comply with global regulations. QUMAS EQMS (formerly ProcessCompliance), a cloud-based solution that provides integrated regulatory, quality and compliance management capabilities within a validated QMS environment, is QUMAS EQMS. QUMAS's data-centric approach lets you manage quality content easily and access and re-use all data. This gives you a comprehensive view into Quality. Interactive quality dashboards from QUMAS provide QMS overviews across all business areas and quality initiatives. Export, email, and scheduling are all possible for reports. QUMAS allows QMS departments the ability to securely, efficiently, and compliantly exchange information in the cloud.

It can seem like a never-ending series of tradeoffs to bring breakthrough products to market within highly regulated industries. MasterControl's GxP software simplifies workflows, so you don't have to compromise quality for cost or innovation with regulation. Complete and connected meets flexible and fast. MasterControl Quality Excellence transforms quality data and processes to a competitive edge. Modern software is the first step in modernizing your manufacturing operations. MasterControl Manufacturing Excellence, from work orders to production records (EBR/eDHR), to logbooks and work instructions, is the easiest way to digitalize manufacturing.

digiQC empowers Site Engineers with a Construction Quality Management Software solution. A quality management system in construction can help you take control, increase visibility, and increase accountability and quality standards across your Quality Assurance team. You can keep an eye on your onsite projects without compromising the quality. Get insight and spot alarming issues before they exceed your budget or project deadlines. Your quality assurance team can record data digitally using a mobile app and a web platform. You can reduce the amount of paperwork and human error that goes into manually filling out data forms. You can create a process that ensures that quality checks are completed at each step. Your site engineers should be able to take and record real-time data during quality checks.

Initially pioneered in one of the most heavily regulated industries in Canada, Elevated Signals provides modern manufacturing software designed to automate and simplify operations via a unified source of truth. Since 2016, the technology has helped fast-growing manufacturing businesses to work smarter, not harder, so they can focus on driving growth. Tailored for ease of use, their GMP-validated platform removes time-consuming mundane tasks and breaks down data silos by unifying real-time information and ensuring complete traceability. This is achieved by connecting end-to-end batch production data, providing instant cloud reporting for one-click compliance, and allowing customization of workflows across inventory, quality, and finance. It also delivers precise inventory visibility and streamlined communication to enable easy access across departments from anywhere. Workers can quickly gain the insights needed to make better decisions, improve productivity, and cut waste.

AQF is a management tool for quality that was developed by experts in quality control. AQF is a complete solution that eliminates the need for paper and allows you to carry out all stages of quality assurance. We offer a modular service that allows companies to get the right product at a reasonable price. The installation of additional modules is not possible if the main module has not been installed. Our AQF module complements its own modules. The AQF module can be used in conjunction with the ERP or software you already use. Manage, share, and create your controls within your organization, as well as your supplier's audits and your procedures. Simplify the process between users and give specific rights to manage outgoing information. Automate the request of documentation to avoid any oversights. You can manage and control temperature and humidity using the Internet of Things (IoT).

QEdge QMS is Enterprise Quality Management Software (EQMS). It optimizes quality and ensures regulatory compliance. Enterprise Quality Management Software (EQMS), reduces the risk for quality process failures, lowers overall costs, and makes organizational processes more compliant. QEdge is an EQMS that allows companies to manage their Quality Management System in a disciplinary regulatory environment. It brings together all quality processes, such as Change Control and Deviation, Investigation and Market Complaints. OOS, OOT and Risk Assessment. Document Control activities, Training Records, and Document Control activities. QEdge, an intuitive and configurable software platform, allows for cross-functional communication and collaboration. It can interface with legacy systems and facilitates error-free, cross functional communication.

Arena's product-centric QMS software allows medical device manufacturers to quickly bring safe and compliant products to the market. Arena QMS connects quality and product processes to streamline new product development and introduction (NPDI). Arena QMS ensures compliance with quality standards and regulations, including FDA 21 CFR Part 820 Part 11 and ISO 13485. Arena QMS improves visibility and traceability by monitoring quality processes in context of bills of materials (BOMs), DMRs and SOPs, as well as specifications, drawings and training plans.

Virje complies to 21 CFR Part 11, 21 CFR Section 820, ISO 13485. Are you overwhelmed by the idea of Part 11 software validation Accessible wherever you are, whenever you work. Automated collaboration and automation can help you reduce paper, lower costs, and increase efficiency. This is the ideal solution for small- to medium-sized businesses. This system was designed specifically for quality control of medical devices. The system is flexible enough that it can adapt to your workflows without having to compromise. Modifiable change order approvals can be configured by employee role or by document type. Notifications to the responsible personnel at each stage of the change process. Ability to identify material dispositions for individual documents. Access to historical and released versions of documents is easy. Quick access to document history. Tracking of locations and distribution of hard copies. Notification of periodic document review.

A holistic approach to managing GMP-regulated manufacturing areas is essential. It involves identifying and monitoring the critical components, such as personnel, facility, and microbial control. By instantly recognizing compliance related anomalies and contamination threats, DeepEyes video-based AI error-recognition solutions close the gap that even the best training and supervision/monitoring leave open. Intelligent DeepEyes solutions automate surveillance by alerting deviations to good manufacturing processes (GMP), in real-time. They provide continuous quality control that goes parallel with the manufacturing process. Operator training is not enough to eliminate the possibility of leakage. Monitoring is essential to avoid product loss, waste disposal issues, downtime, and other safety hazards.

The AssurX platform is a powerful software platform for enterprise quality management (EQMS) and regulatory compliance to reliably communicate and coordinate information, documentation, and activities. AssurX allows regulated businesses to quickly identify and control quality issues and risk exposure to avoid quality or noncompliance problems while improving workflow. AssurX QMS software is uniquely configurable to fit any established or dynamic business requirements. The system creates an electronic workflow of tasks, alerts, escalations, and approvals that can be automated to the desired level, mapping precisely to real-world operations. No other system is easier to deploy, configure, and modify. AssurX solutions integrate seamlessly to create a connected quality system. Solutions include audit management, corrective actions, training management, compliant management, document management, change control, risk management, EHS incident management, and more.

Software for compliance management in the cannabis industry. Optimized Cannabis Compliance Software. The medical marijuana industry is highly regulated. Most states require that cultivators, distributors, and processors keep track of every ounce of cannabis, as well as any edibles they sell or throw away for quality issues. You must keep a record of all transactions, from cultivation to final sale, in order to be compliant with the law in the cannabis industry. The constant changes in the medical marijuana market, along with the need for compliance and risk reduction, cannot be managed using traditional software or manual templates. The Features You Need to Be Successful. Otter Systems Compliance Management Software is a central platform that tracks regulatory requirements, organizes compliance documentation, and manages compliance processes. Features include: Cannabis Document Control; Policy Management; Change Management; Supply Chain Control.

Secure Audit, Risk, Compliance, Quality Software. Available in both Cloud-based and On-Premise deployment options. Auditrunner provides granular encryption and role-based access controls for audit files and documents-at-rest. All data is protected. Our platform has automated over 3000 business processes for companies around the globe. These are just a few examples of the GRC platform modules. Cloud-based and On-Premise. Just deploy and begin using. The platform's seamless integration allows you to start enjoying the benefits within weeks of launch. The platform's low-code design allows for customization and compliance with any standard or regulation. You can operate in a fast-moving, constantly changing regulatory environment and comply instantly with a multitude of different legislation without assistance. Our ease of use is unmatched.

Quality is a continuous process. It is a conscious practice to stay ahead of the business world. Quality is a key ingredient in core industries such as pharmaceuticals. Acceptability, approvals and success are all dependent on it. Pharmaceuticals are a highly regulated sector. Stringent regulations make it more difficult to manage business processes. Integrative quality management systems are essential for ensuring continuous review and reinvention of activities as well as internal processes. GMPPro is a robust and meticulous quality management system from Motto Systems that can be used to address quality issues at all stages of drug development. GMPPro, a precision quality management system, can encompass the entire spectrum of production, quality assurance, engineering in systemic Integration and as independent solutions modules.

Redzone has taken the CPG, food and beverage manufacturing markets by storm thanks to its digital production system, which was specifically designed for continuous improvement and lean manufacturing. Customers report and sustain productivity increases of 30+% by empowering their frontline workers after their initial 90-day deployment. The Typical Outcomes - Rapid double-digit productivity increases - A system for collaborating with the workforce that reduces turnover - A culture that encourages continuous improvement and is driven by your employees, and maintained over the long-term You can connect all levels of your business with specific modules for production, quality, and maintenance. This will allow you to identify issues before they become problems and fix them!

Manual quality management processes can be costly and ineffective. Verint's Quality Bot automates quality programs to save money, improve quality and reduce compliance risks. Start today to see 5x ROI. Does your quality management program work? If you only screen a small number of calls, you may be able to hide non-compliant interactions, which could lead to fines, lost sales, or worse. Verint can help. Most contact centers review only 1 to 3% of their calls. This severely limits your capacity to identify risks, manage quality and comply with regulations. Verint Automated QM can automate your entire quality management process, helping you achieve better compliance. Evaluate calls, identify noncompliance, and assign coaching for 100% of voice and SMS interactions. This will give you a deeper understanding of your organization's service standards and compliance.

Organizations can eliminate information-caused incidents with AcceleratorKMS. Workforce development with mobile-ready content. Review and update information. Streamline authoring to save time and money. Find efficiencies and monitor work. Reduce time and money spent on onboarding. The Accelerator is a digital content ecosystem that integrates digital content in an intuitive package that makes complex tasks simple. Our goal is to make information more accessible for front-line workers and to make operations safer. Workers can access digital Standard Operating Procedures (SOP), policies and training content instantly from their mobile devices to reduce the risk of human error. Standardizing all operational content will reduce the risk of information-caused incidents. AI-assisted procedure authoring will make it easier to use. Standardization reduces administrative burden and management effort.

Online document management makes it easy to create and manage documents. This prevents lost printed copies and a lack of organization. All information can be gathered in one place, making it easy to track and address any nonconformities. To aid you in decision making, define, collect and analyze KPIs using comparative charts. You can plan and execute actions to address opportunities and risks in a controlled and simple way. Get rid of spreadsheets and printed copies. Access file control in a cloud database with 24/7 access from any device and location. Optimize document review, approval, and elaboration. Manage access permissions, and receive automatic notifications about document changes or expiration dates. Genebra always has the most current version of any file that is uploaded. Don't waste time looking through multiple spreadsheets and don't lose any revisions.

To optimize your shop floor, combine manufacturing, MES and supply chain software. Learn how DELMIAworks, formerly IQMS, can help you improve visibility into every aspect your manufacturing operation and solve the most difficult production problems. Reduce downtime and increase manufacturing efficiency, quality, profit margins, and quality. Real-time data access across the entire supply chain can improve decision making. All ERP, manufacturing, MES and supply chain requirements can be handled by one system. Automating your business can lower your investment and maintenance costs. Our simple-to-use solution will double your plant output, eliminate human error, and improve the efficiency of production planning. To eliminate unplanned downtime, increase throughput and reduce downtime, manage, track and monitor all aspects of the production process. OEE graphs and charts are dynamically updated with performance data and quality data in real time.

Caliber's Integrated Quality Management Platform - EPIQ stands apart from other generic quality offerings on the market. Caliber provides seamless quality management by integrating and functionalities across departments in a way that is unmatched. This platform also provides capabilities that go beyond the regular quality management requirements. It can be used to build foundations for quality metrics, performance analytics and CPV. Automation is a major investment for many companies. However, there are still inadequacies when it comes to information sharing between departments. Quality Assurance departments must see the effects of deviations across all departments. Many planned and unplanned changes must be reviewed and closed by more than one department. Interdepartmental transactions are a key part of risk mitigation.

In today's pharmaceutical manufacturing environment, it can be difficult to maintain consistent product quality and quality processes. To meet regulatory requirements, industries like the Pharmaceutical, Biotech and Life Sciences must maintain Good Manufacturing Practices (GMP). You must not only meet GMP requirements, but you must also be capable of proving it.

Enterprise Quality Management Software in cloud for life sciences. Technology plays a crucial role in ensuring that QA is aware of any issues as they arise in today's complex operational environment. You can gain insight into your quality management system's performance and the current state in your operation to be more proactive and reduce risk. Montrium's Enterprise Quality Management system (EQMS), was designed to help life science companies tackle the content management challenges they face head-on. Each module of the SharePoint QMS can be used separately or as part of a fully integrated quality management platform. These modules can be used on-premise or in a cloud environment. These modules are ideal for pharmaceutical companies, contract manufacturers, and medical device companies. Built to comply with GMP/GCP requirements.

icmInspector automates control, review, and audit processes. It includes a central component responsible for administration and management, and a mobile app for Android. Improvement of the quality of the organization through the use of modern inspection, control, and interial audit procedures that enable the detection of irregular or undesirable situations in a dispersed, real-time manner. By replacing paper versions with electronic versions, you can reduce operating costs and minimize time spent on material preparation and distribution. Tools that enable fast data collection, protect against omissions and offer the possibility of scheduling work can increase the efficiency of those who are responsible for audits and controls. Eliminate fraud, abuses, and errors in the control process by recording metadata about data collection and enforcing only logically permissible answers.

Reva QMS, a software-based Quality Management System, is available. Our solution helps organizations organize, manage, report, and track business-critical documents. It also aligns their business processes to conform to relevant industry standards, laws, regulations, and specifications. Reva QMS is specifically designed for highly regulated industries. It helps organizations automate their paper processes and ensure regulatory compliance. It offers a complete set of functions and capabilities that are specifically tailored for highly regulated industries. This allows them to achieve greater operational transparency and adhere to industry standards, best practices, rules, and regulations. It offers a simple browser interface that makes it easy to manage business processes.

Greenlight Guru is the only product development and quality management platform designed specifically for medical device companies. The Medical Device Success Platform helps companies get safer products to market faster, simplifies FDA and ISO regulatory compliance, and provides a single source of truth by connecting the management of all quality processes like CAPAs, risk, audits, document control, training, design control, and more. Device makers across the globe are replacing their outdated paper-based and general-purpose legacy quality systems with Greenlight Guru to push beyond baseline compliance and achieve True Quality.

Vault QMS ensures quality and compliance to GxP. Vault QMS integrates best practices and automates workflows to bring all parties - pharma, biotech companies, contract manufactures, and suppliers - into quality control processes for better visibility and control. You can easily bring departments, sites and suppliers, contract manufacturers, contract testing labs, or other partners into continuous quality improvement. Automated workflows and best practices will increase operational efficiency. Unified risk management can improve visibility across products and processes. A unified suite quality applications will improve speed, efficiency, compliance, and GxP. You can easily enable quality management processes by incorporating best practices for deviations, internal and external audits and complaints, as well as change control, CAPA and quality risk management.

TIPQA is a tool that companies use to make continuous and measurable improvements in customer service, productivity, profitability, and customer service. Our QMS software allows industry leaders and managers to monitor compliance and manage quality throughout their supply chains. TIPQA QMS Software will support best practices in quality management and help you create a comprehensive continuous improvement plan for your company. Numerous companies who require high-quality products and strict quality control have found success with the TIPQA quality management software. TIP Technologies is more experienced in complex business processes within regulated manufacturing environments than any other solution provider. TIPQA's quality management solution allows users to be flexible, adapting to changing markets and quality demands. TIP Technologies is constantly improving its quality management system.

Your supervisors, trainers and Quality Assurance teams can empower your agents to improve customer interactions. A user-friendly interface allows you to review recorded and live-monitored calls and sync voice and screen recordings. Automated analysis of interactions to provide actionable insights. A sophisticated call center quality management system will help you improve service quality, assess call-handling effectiveness, and ensure agents adhere to scripts and processes. Use an intuitive interface to manage your team's performance. You can listen, monitor, score, and evaluate agents. Then, you can provide effective coaching and eLearning. To coach agents and improve KPIs, provide e-Learning resources and packaged call content. Perform evaluations quickly, efficiently, and easily. Agents can excel with in-depth performance reporting.

Serious software is essential if you are serious about quality and safety management, inspections, and inspections. Multiply this number by the number of inspections that have been conducted over the life of thousands of serial-numbered tools and equipment, and you'll see why specialized software can help you save time and cut costs. FTQ360 understands the challenges of oil and gas inspections and testing, and the details that go into documenting them. This is especially important when millions of dollars, lives, and the environment are at stake. Every day, you must hold your operations to the highest standards. All of this must be done in a way that is compliant with regulators, customers, and litigants. This is not always easy. We can help if you are serious about a global compliance platform to streamline your quality and safety-critical inspections, and keep it all under control.

iCompliance, a comprehensive digital platform, is designed to streamline Quality, Health, Safety, and Environment management, Environmental, Social, and Governance initiatives, and Governance, Risk, and Compliance processes for organizations in various industries. Our software provides tools for incident reporting and management, audit management, corrective action, and more. These tools help ensure compliance with regulations, standards, and safety, promote environmental responsibility, track ESG performances, engage stakeholders, manage regulatory requirements, internal control, and risk mitigation strategies, and ensure regulatory compliance. iCompliance's customizable workflows, real time analytics, integration options and mobile accessibility, as well as multilingual support, empower organizations to achieve operational excellence and mitigate risks.

Seerene's Digital Engineering Platform uses software analytics and process mining technology to analyze and visualize your company's software development processes. It uncovers weaknesses and transforms your company into a well-oiled machine that delivers software efficiently, cost-effectively and quickly with the highest quality. Seerene gives decision-makers the information they need to drive their organization towards software excellence at 360deg. Reveal code that is often broken and kills developer productivity. Reveal features that are not executed by end-users or have a mismatch in developer time and created user value.

Smart software for recipe management. Stop using Excel or ERP as a band-aid solution. Eclarion makes recipe management easy with QUID, allergens and nutritional values. Today's customers have higher expectations and are more demanding. Eclarion can deliver product specifications quickly and easily. We are constantly improving and optimizing the recipe management process together with 150+ Quality Managers. This allows for a simple path from raw material to finished product. It is highly practical and efficient. Eclarion will do all the heavy lifting for your next audit or inspection. Integrating external datapools like PS in Foodservice or GS1 will give your ERP system a boost and maximize results. In minutes, you can create your first recipe. Eclarion is connected to the PS in Foodservice supplier database. Predefined ingredient information is available for frequently used ingredients. Avoid mistakes and unnecessary typing. Eclarion will save you a lot of time.

In just 30 days, you can triple your innovation speed and improve your continuous improvement. Unifize is a software platform that facilitates collaboration in innovation, quality, CI, and other areas. This allows manufacturing companies to bring better products to market faster. Unifize works in any environment, no matter if you use it for one function or all. Templates are customizable to your needs and allow you to connect all of your processes. Unifize is the only PLM platform that focuses on bringing together teams in a real-time collaborative environment. This allows them to solve problems and manage important innovation processes. Look no further if you are looking to upgrade to a complete Quality Suite. Unifize is an eQMS that makes quality processes collaborative and simple to follow. Don't just pay lip service to your APQP/PPAP process. Teams can come together for a dedicated conversation in real-time about each record.

SoftTech Health has the best quality management software tools in healthcare today. Because they integrate seamlessly, you can streamline all of your quality management tasks with one simple-to-use software package. Our Accreditation Manager will help you manage any upcoming inspections. It includes tools that allow you to compare and copy work from previous inspections. You can automatically track evidence of compliance and make sure nothing slips through the cracks. You want to make sure that all requirements are met. Reduce time and effort in coordinating, tracking, and reporting on audits. Streamline the tedious process of gathering supporting evidence. Accreditation Manager automates these processes, increasing compliance and the bottom line.

Quality Link 7 is a combination of people and technology. It builds on our proven platform to help organizations automate processes, save time, and comply with regulatory requirements. Quality Link's document management system improves efficiency and eliminates the need for manual paperwork. This module will store and manage every document you create. This module allows you to print "uncontrolled" copies and perform other document-related tasks. You'll see a reduction in clerical tasks for quality staff by up to 90% with the improved organization. Our software converts existing documents from your previous management system and requires no learning curve. You won't have to lose your favorite applications as they can be easily integrated. Quality Link makes manual document maintenance obsolete and eliminates the need for constant monitoring.

Solutions that are user-friendly for modern quality management and modern working environments. orgavision assists organizations in setting up a living system of management. Version management, signature lists and releases, as well as task distribution are all supported by orgavision. Manual or paper-based methods can be error-prone and require a lot more administration. They also have a limited ability to distribute precise information. You create the content, and automatisms do the rest. Reliable and safe. Our SaaS solution is easy to use - you can start right away, without the need for installation via your browser. You can instantly access the most recent version without having to worry about maintenance, updates, or backups. Technical support is also available at no cost. Our secure German data center hosts the orgavision cloud. You need to sign the receipt if you want to share important information with all production teams.

AirManual makes it easy to combine a checklist and guidance that explains what each step is. Ideal for training and recurring processes. AirManual allows teams to document their processes, training, and onboarding. AirManual combines a user-friendly tool with free consulting. We'll help you prioritize and address your most pressing issues. Our customers enjoy a better quality of life, faster growth, and longer vacations as a result. A home for documentation, processes, and training. Your team will find the documentation they need and be able to solve their own problems. AirManual is a tool that works for all teams. AirManual works for every team. Start in the most important area and then scale it up as you need it. Stale documentation is gone. It's easy for your team to review usage and get feedback. AirManual users who are new to the platform can receive free consulting. We will help you move faster and avoid common pitfalls.

AuditComply is a Belfast-headquartered Enterprise Risk Management Platform. Comprehensive solutions for Quality, Compliance, Risk, and EHS. SaaS-based solution that helps you spot hazards/issues and monitor risk. It also helps you to manage uncertainty and boost your performance. The company works in highly regulated sectors such as Automotive, Food & Beverage and Oil & Gas. Key clients are located throughout the UK, EU and US, Middle East, Asia Pacific, and Middle East regions. AuditComply combines the enterprise workflow with the speed and agility to deploy a mobile-first application. Our enterprise customers choose us because we deliver value from the first day. We adapt to change seamlessly to meet customers' daily needs, promote visibility and reduce costs, and drive operational efficiencies while anticipating and managing enterprise risks.

Without a proper Quality Assurance (QA), issues such as missed deadlines, incomplete dynamic fields, and overcommunication can all arise. It is becoming more important to ensure that privacy legislation is adhered to internationally as privacy laws evolve and sometimes transform. Munvo's CampaignQA(c), ensures compliance with all regulations. This technology can be used to complement your marketing automation system, and to improve overall marketing execution in a timely manner. Automate the validation of outbound and inbound marketing campaigns, and monitor the results using robust alerting features and reporting. Easy-to-use drag-and-drop interface allows you to manage contact frequency controls (no programming required). Allow rules-based validation for marketing data/marketing datamart quality.

ZipQuality, a software-enabled medical device service, helps companies bring new products to the market. Our collaboration platform allows agile teams to make rapid design changes while maintaining regulatory compliance. System (processes and tool) pre-configured; no need to change your quality system. The integrated system is able to handle rapid design iterations in product documentation. Your team will be guided by experienced consultants at every stage. Software tools that are fully featured, scalable, and built on the powerful ENOVIA platform. Our integrated system allows for rapid design changes, while keeping data and documentation in sync. All records are maintained in a audit-ready condition. Product requirements, Hardware requirements, Software requirements. We have a deep understanding of complex, software-intensive devices. ZipQuality is a structured documentation system that supports good systems engineering and efficient risk management. It also provides clear traceability.

OurRecords is a cloud-based credential management system that can be used by healthcare, mortgage, and food businesses. OurRecords allows companies to use a single platform for managing and storing verified credentials and records. Top features include supplier/vendor management, workforce prerequisite program, proactive alerts/notifications, document distribution, centralized documentation, and automated reports.

You can now focus on delivering safer and more effective products faster by eliminating repetitive, manual tasks. SmartSolve Postmarket Suveillance by IQVIA is a SaaS solution for postmarket surveillance. It provides best practices for centrally managing all postmarket surveillance activities. Fusion is a SmartSolve/RIM Smart user event. It provides in-depth education on timely and relevant quality topics and regulatory topics, as well as practical insights and tools that can be used within any Life Sciences organization. Fusion began as a live SmartSolve user event. It has expanded over the years to include both virtual and live events for SmartSolve and RIM Smart users. IQVIA SmartSolve™, Regulatory Connector, simplifies, automates, and integrates your compliance response times. Connected Intelligence, our innovative, interconnected approach to operational efficiency, is what we call Connected Intelligence.

Your business's lifeblood is quality services like programming content, live sports broadcasts and data backhaul. Satellites can also provide high-speed data access for customers. The current management tools do not allow you to optimize these services as they only show performance metrics for a single device, such modems, antenna control units (ACUs), high power amplifiers (HPAs) or other equipment in the teleport. They also don't identify which devices are supporting specific services to customers. Multiple, unconnected tool sets are required for different types technologies. These include Monitor & Control (M&C), management systems for VSAT networks, and Network Management Systems (NMS), for RF equipment. Carrier Monitoring Systems (CMS), to manage carriers. This allows for the identification and resolution of the root cause of an issue. difficu

Developers can track errors and monitor performance to see what is important, find faster solutions, and continuously learn about their applications, from the frontend to backend. Sentry's performance monitoring can help you trace performance issues down to slow database queries and poorly performing api calls. Sentry's application performance monitoring is enhanced by stack traces. Identify performance issues quickly before they cause downtime. To see the entire distributed trace from end to end, you can identify the API call that is not performing well and highlight any errors. Breadcrumbs help you make application development easier by showing you the events that led to the error.

A QMS that covers all stages of product life from Design Control to CAPA. We train your entire team, and provide support as needed. Enzyme Consulting, LLC. Enzyme Consulting, LLC. can assist you in customizing and implementing your Quality System. Enzyme's team can be reached for follow-up calls or to answer any questions after your onboarding. Enzyme's QMS was built by industry veterans who were frustrated by existing QMS systems. It was designed for all life sciences companies and we paid particular attention to the challenges of creating FDA-regulated software. With the support of our dedicated consultants, you can bring your product to market confidently. Our consultants have first-hand experience in the medical device industry, and an acute ability to accurately assess risk. They understand the challenges of product development.

EasyQA Software Development Kit can detect and fix crashes in Android or iOS mobile apps Save time You don't need to reproduce the crash in order to determine its cause. Just send it to the Crashes Page within your project and review all details with a log file Delete duplicated crashes If you are unable to debug your code or know of the crash and don't wish him to appear in your system, click on the Delete button Check log files on your phone If your application crashes, restart it. Click on the notification to confirm. You can instantly check the log file to determine the root cause.