Best CAPA Software of 2024

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.

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.

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.

ZEBSOFT GRC & ISO management platform is a holistic approach for managing Governance, Risk & compliance. ZEBSOFT's intuitive web interface makes it easy to manage ISO standards (9001, 14001 and 22301), 27001, 27001 and 45001 and many others. ZEBSOFT has powerful integrated modules for Risk, Quality, Environmental, InfoSec, Compliances, policies (templates included) & documents, equipment & asset management with maintenance/calibration/testing planning. Improve internal communication, assign ownership, plan, and conduct audits. To see the full potential of ZEBSOFT, book a demo today!

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.

You can quickly control your indicators and get better results. Our strategic management software will allow you to plan more efficiently, organize your routine better, and manage your team in a culture of results. Our software goes beyond just organizing your routine. Strategic management software can help you improve your business results and engage your team to achieve your goals. Performance indicator software can help you: Reduce the time it takes to collect, validate, and consolidate KPIs. Identify and plan for solving problems. All levels of the company should be able to see your results. Your entire team should be involved in a results-oriented culture. Your goals will be achieved. Allow everyone to have the conditions necessary to reach the goals and objectives. Facilitate the delivery of Strategic Projects by engaging people. Increase productivity of your team and make decisions faster and more confidently!

adWATCH – AE assists pharmaceutical companies to report adverse events that may occur during clinical trials. adWATCH – AE provides a quick and efficient way for a reporter at a clinic or hospital to generate and manage Adverse Event Reports (AERs), and report to regulatory agencies and government agencies. A negative or dangerous effect is one that a patient experiences due to the use of drugs or medical devices. Adverse event reporting involves the tracking of all medical complaint cases. This allows for the generation of MedWatch reports, CIOMS and additional reports for management. adWATCH – AE allows researchers, physician-investigators, Contract Research Organizations, clinical trial specialists, and other healthcare professionals to create and file AERs in FDA mandated MedWatch or CIOMS format.

These workflows will help you create everything you need for a 510(k), and create quality records for 21 CFR Part 820 when you are ready to sell your device. Built-in tools for creating policies, procedures, or work instructions. With customized quality management reports, you can track non-conformances, deviations and CAPAs. Keep your team trained as you improve and scale your policies, workflows, and procedures. Automate validation testing for devices, apps, web and custom-made software. Reduce the time and resources required for lengthy testing, reporting, approvals, and other tasks. All your policies, procedures, artifacts can be converted into traditional documents for audit review.

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.

All the information you need to test specifications, supplier communications and test failures, as well as lab notifications, corrective action, and performance metrics, is at your fingertips. LINK Services is a Product Compliance Testing program management software that focuses on product and material conformity. It provides tools for supply chain partners to communicate tasks and analytics related to product and material test programs and specifications, test orders, lab reports, corrective actions and bills of materials and related product quality management activity. LINK bridges the gap between brand/retailer enterprise system (e.g. PLM, ERP/SAP), vendors, and analytical testing labs (in-house and third-party). It harmonizes and centralizes data into a single, lab-agnostic, system.

iDoc is a document management system that is efficient. Automates and controls the documentation process, including distribution, organization policies and standard operating procedures. It is robust and secure in managing document management systems. It also provides real-time visibility. It streamlines all processes, including creation, review, approval, archival, and archival, and supports multiple files in controlled ways. Integration with training management system to assign training and to remove incorrect documents. This ensures accuracy for end-users and tracks compliance. Automated documentation, document retrieval with search/indexing capability, and document archive. You can easily set up labels, descriptions, and tags to help you organize information and keep track of documents. Keeps track of all documents and tracks any changes. This provides an audit trail that reports on documents and data fields.

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.

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.

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.

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.

Manufacturo, a SaaS-based platform, is designed to simplify manufacturing operations. It can be tailored to suit any industry but is most useful for hi-tech and innovative manufacturers whose productions are complex and non-conformances need to be identified and tracked back to prevent potential problems. Manufacturo is a collection of applications that helps in creating work instructions and collecting shop-floor information, controlling inventory, as well as managing non-conformance.