Alternatives to MediaLab Intelligent Quality Engine (IQE)

14,000 laboratories. 125 countries 98% customer satisfaction! LabWare's range of laboratory automation solutions can help you increase productivity, throughput and efficiency, as well as data integrity and compliance. LabWare offers flexible deployment options. Laboratories that are looking to deploy in a matter of days can choose the fully-validated and cost-optimized SaaS LIMS with best practice workflows. Laboratories who require a fully customizable enterprise-level LIMS/ELN for their business can choose from either self-hosted or flexible cloud deployment options. LabWare users have access to world-class features like lot management, sample and stability management, instrument interfacing and workflows and dashboards, inventory and COA management, COAs, barcoding and many more.

isoTracker Quality Management is a popular cloud-based quality management software (QMS) system. It is used on a worldwide basis by businesses to manage their ISO 9001, ISO 13485, ISO 22000, ISO 17025, ISO 14001 systems...plus many others. It is a modular product which can be configured to meet an organization's specific requirements and is competatively priced with superg customer support. Any module combination of Document Control, Complaints, CAPA, Audits, Training, Non-Conformance and Risk can be subscribed to.

The SBS QMS Suite consists of 5 software modules that work together for efficient Quality compliance: 1) SBS Quality Database - CAPA / 8D corrective and preventive actions (CAR) with root cause analysis - Nonconformance management - Risk analysis including FMEA, SWOT, interested party risk register - Internal, customer, and third-party audit management - Environmental Health and Safety (EHS / HSE) management 2) SBS Ground Control - Employee training management (LMS) - Self-Paced training - Change control - Document control 3) SBS Asset Tracking Database - Calibrated equipment control - Preventive maintenance - Asset inventory management 4) SBS Inspection Database - Record incoming material, in process, and final product inspection data - Generate real time SPC charts - Inspection plans and Control Plans - Archive data for further statistical analysis 5) SBS Vendor Management - Maintain an approved vendor list or AVL - Develop vendor / supplier qualification plans - Maintain vendor / supplier qualification history Modules may be purchased separately or in any combination. On-premise and cloud-based options are available. Free demos are available for download or contact us for a cloud-based demo.

Dot Compliance offers the industry's first ready to use Quality Management Solution powered by the Salesforce.com platform. The Dot Compliance solution includes an extensive set of off-the-shelf ready eQMS and compliance pre-configured processes, enabling customers to deploy quickly and cost effectively. Dot Compliance ready to use solutions include full project validation services and product validation packages. Dot Compliance offers the industry’s most cost-effective quality and compliance management solution available, allowing users to quickly deploy flexible and scalable solutions. Automate core quality processes such as Document Management, Training Management, CAPA, Audits, Customer Complaints, Change Management, Supplier Quality, and more. Our solution is fully configurable and offers seamless integration abilities, with easy adaptation and implementation of customer’s specific requirements.

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.

Document Control is MediaLab’s document management system. Our online solution empowers lab directors and supervisors to manage their policies, procedures, forms, job aids, and worksheets using configurable review settings, custom approval workflows, automated employee sign-offs, and more! Reduce time spent chasing approval and review signatures while benefiting from email notifications and personalized to-do lists for employees. MediaLab's Document Control supports: • Digital records and version control of all documents, • Standardization across all documents from all sites, • Electronic signatures that meet 21 CFR Part 11 standards, • Customized approval workflows and processes, • Robust searching to easily locate specific documents, and more!

SimplerQMS offers a cloud-based Quality Management Software, specifically designed for the Life Science industry. SimplerQMS helps ensure compliance with various regulatory requirements, including FDA 21 CFR Part 11, EU Annex 11, GxP, cGMP, GAMP 5, GDPR, EU IVDR & EU MDR, ISO 13485:2016, 21 CFR Part 820, and ICH Q10, among others. The system is fully validated according to GAMP5. The system offers a range of Life Science QMS modules such as Document Control, Change Control, Training Management, Supplier Management, Complaints Management, Non-Conformance and Deviation Management, CAPA Management, Audit Management, Technical Documentation Management, Risk Management, Quality KPIs and more. SimplerQMS integrates with Microsoft Office and allows users to work with documents in applications such as Word, PowerPoint, and Excel. Overall, SimplerQMS delivers efficient, paperless workflows that align with the compliance requirements of the Life Science industry.

The Avalon Laboratory System, which is sophisticated and HIPAA compliant, was specifically designed to manage production and billing requirements for clinical, esoteric and toxicology labs. Computer Service & Support (CSS) developed this modular laboratory information system that offers a variety of features for reference laboratory automation. This solution also includes modules for microbiology and pain management, toxicology, scheduling, remote laboratory, SQL Access and electronic medical records. It also offers pharmacogenomics and revenue cycle management.

BPAQuality365, a QMS software, can be used in your secure Microsoft 365 cloud. It leverages tools used daily by collaborators and does not require you to change your user habits. It is modern, compatible with all devices, adaptable to your specific needs, and powered through innovative M365 technologies. The app includes powerful compliance document management, audit, non-conformance, CAPA action, process and process maps, incident, change, risk, FMEA, SWOT, equipment, health, safety, environment modules compliant with ISO 9001, FDA Part 11 and medical regulations. The QMS app integrates with Teams discussions and users can ask the QMS while chatting in Teams and share QMS card with their colleagues. You can go further to achieve your Quality 4.0 goals by combining powerful AI features with best-in-class workflow automation and business intelligence. BPA's Microsoft Preferred status allows you to customize your QMS to meet your needs, share knowledge with your power users, and learn about M365 technologies.

Artintech ERP is a comprehensive enterprise resource planning solution designed to optimize and streamline your business operations across various departments. Tailored for small to medium-sized enterprises (SMEs), Artintech ERP offers robust functionality with a user-friendly interface, allowing businesses to seamlessly manage their resources, inventory, human capital, finances, and customer relations all in one integrated platform. Why Choose Artintech ERP? * User-Friendly Interface: Designed for ease of use, Artintech ERP minimizes the learning curve, ensuring a smooth transition and quick adoption across your organization. * Cloud-Based Flexibility: Access your ERP system anytime, anywhere, with our secure cloud-based solution, which provides the flexibility to manage your business on the go. * Comprehensive Support: Our dedicated support team is available to assist you every step of the way, from initial implementation to ongoing maintenance and updates.

The [FP]-LIMS modules rely on a powerful SQL database solution. These modules allow for quick queries and data processing. We guarantee maximum user friendliness. Our job server is the central element of automation, which executes event- and time-controlled tasks. To monitor limit values and send an alarm message (email, message on monitor, etc.) automatically. When they are exceeded. Modern LIMS software, including modules such as inspection planning, workflow management, and analysis management, can help you design your quality management system in the most efficient way. This will make your production processes more efficient.

SolvoNext – NCR CAPA empowers small and medium-sized factories to replace outdated paper-based NCR and CAPA processes with a robust, digital-first solution. The platform guides teams through a structured workflow—starting with NCR initiation, moving through root cause analysis, recording financial data, and ending with secure approvals—all while maintaining a complete knowledge library. Interactive dashboards display key metrics like NCR status, departmental tracking, and monthly progress, helping leaders make quick, data-backed decisions. Its COPQ tracking feature calculates the financial toll of inefficiencies, waste, and defects, giving organizations a clearer view of quality performance. Built-in quality tools such as the 5 Whys and Fishbone diagrams make problem-solving systematic and collaborative. Users can assign role-based permissions, manage multi-level approvals, and receive automated alerts for faster communication. Optional AI integration enhances the platform with predictive analytics, advanced diagnostics, and automated reporting tailored to each plant’s needs. SolvoNext ultimately improves compliance, transparency, and operational efficiency across all manufacturing environments.

A web-based software suite for medical device companies that automates their processes and simplifies regulatory compliance. Modules include Audit Management, CAPA and Complaint Handling. Designed from the start for ISO 13485 compliance and 21 CFR Part 11 compliance.

Software designed for ISO and BRC compliance fulfills the criteria of various management standards, such as ISO 9001, 14001, ISO 45001, ISO 27001, and the BRC benchmarks. It features a robust and user-friendly CAPA system that effectively documents continuous improvement initiatives, non-conformities, root cause analyses, corrective and preventive actions, and key performance data on losses. The software also ensures efficient version and change control for system documentation and regulated forms. Additionally, it implements location-based controls to restrict user access to documents based on their specific roles. There is a compliance evaluation tool that details the necessary compliance obligations, assigns departmental responsibilities, and provides guidance on adhering to legal and other relevant standards, applicable to both single and multiple standards, including ISO 9001, ISO 14001, ISO 45001, ISO 27001, and others. Furthermore, it simplifies the qualification, ongoing evaluation, and performance improvement of suppliers, service providers, and contractors through tailored risk management workflows, assessments, scheduled re-assessments, and focused action logs. This comprehensive approach ensures that organizations not only meet compliance standards but also foster a culture of continuous improvement and accountability.

Compliance Manager is a SaaS platform designed to facilitate the oversight of various operational elements: Documents - Users can add, update, archive, and manage their Policies, Procedures, Forms, and Templates efficiently. Projects - The application streamlines project management and documentation, enabling team members to collaboratively share essential project details. Tasks - It allows for effective management of tasks, audits, nonconformities, corrective and preventive actions, complaints, and incidents. Alerts - The system includes email alert management to ensure timely completion of corrective and preventive actions. Incidents - Users can effectively manage incidents, conduct investigations, implement resolutions, and perform root cause analysis. Training - It offers tools for overseeing employee records, tracking training logs, and conducting appraisals. Suppliers - The platform assists in managing supplier records and evaluating their performance. Reports - Users can generate comprehensive reports on Audit Results, Root Cause Analysis, Training, and Supplier Performance, thus enhancing overall operational efficiency. With its robust features, Compliance Manager ultimately supports organizations in maintaining compliance and improving their overall performance.

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.

ExtraView serves as a comprehensive software solution designed for enterprises, focusing on business process management and global quality management systems, particularly in areas like CAPA, adverse event reporting, food safety, bug tracking, change management, and customer support. Users can choose between pre-built solutions or tailor their own specifications to meet unique needs. It can be deployed as a cloud service or installed on local servers, making it versatile for various operational environments. The platform is user-friendly, allowing for easy configuration while also supporting the implementation of fully validated systems for incident management, CAPA, adverse event reporting, root cause analysis, clinical trial data management, and food safety initiatives. Additionally, it facilitates the establishment of bug-tracking, customer support, requirements management, and other vital issue-tracking systems. A noteworthy aspect is that many users can benefit from a robust, free downloadable version of the software. Furthermore, financial organizations often utilize ExtraView to enhance their systems for auditing, ensuring corporate governance, and managing risks effectively. This adaptability makes it an essential tool for a wide range of industries looking to streamline their workflow processes.

Wavefront LIMS is an advanced browser-based application renowned for its versatility and user-friendly interface. Tailored to meet the specific needs, workflows, and personnel of your laboratory, Wavefront LIMS offers unparalleled flexibility. Accessible via any computer on the corporate intranet/extranet, it ensures seamless connectivity across your organization. Designed for simplicity, Wavefront LIMS minimizes the learning curve, accelerating the return on investment. Say goodbye to manual data entry and hello to heightened operational efficiency. Wavefront LIMS effortlessly generates electronic data deliverables and seamlessly integrates with laboratory instruments and ERP systems, facilitating comprehensive process automation. With full configurability, your laboratory can adapt to evolving requirements, minimizing time, costs, and reliance on external vendors.

Workflows are specifically developed to assist you in preparing all necessary components for a 510(k) submission, while also ensuring compliance with the quality record requirements set forth in 21 CFR Part 820 as you prepare to market your device. These workflows come equipped with tools to facilitate the drafting of essential policies, procedures, and work instructions. Furthermore, you can monitor non-conformances, deviations, and CAPAs through tailored quality management reports. As your processes evolve and enhance, you can ensure your team receives automatic training updates. The system also automates validation testing for devices, applications, websites, and custom software tailored to your business needs. This automation significantly reduces the time and resources that would otherwise be consumed by extensive testing, reporting, and approval processes. Additionally, you can compile all your policies, procedures, and artifacts into standard documents, making them readily available for audit evaluations. Overall, this solution streamlines the compliance and validation processes, thereby enhancing operational efficiency.

Automate the identification and resolution of problems in your organization and supply chain. This is one of the most trusted CAPA software applications. It has been trusted by thousands of users worldwide. CAPA Manager corrective actions software automates the assignment of corrective actions, notification, investigation and reporting. It prevents errors in the control of the entire CAPA process from initiation through investigation and closure. CAPA Manager meets all requirements of the most important quality management standards, including ISO 9001, AS9100 and TS 16949. It maintains records of root-cause and corrective actions, and provides pre-defined workflows with approval gates.

QualityKick is a cloud-based Quality Management System (QMS) tailored for the biological sciences sector, designed to enhance compliance and streamline various quality management processes. It offers a suite of modules, each addressing critical components such as document control, training, change management, incident tracking, CAPA (Corrective and Preventive Actions), risk evaluation, qualification, and supplier and equipment audits. Being a web-based platform, it ensures accessibility from any location and on any mobile device, including computers, smartphones, and tablets. New users benefit from an automated guided tour upon their initial login, facilitating a smoother onboarding experience. The system supports document editing with MS Word and enables a customizable review and approval workflow, enhancing collaboration and efficiency. Various event types, including deviations, nonconformities, and customer complaints, can be configured to suit organizational needs. Additionally, it allows users to establish CAPA plans, document necessary actions, and assess their effectiveness, making it a comprehensive solution for quality management in the pharmaceutical, biotechnology, and medical fields. With its user-friendly interface and robust features, QualityKick is poised to transform how organizations manage quality compliance.

Labor intensive processes in textile and apparel manufacturing labs are a tradition. LLMS improves efficiency by automating data collection and data analysis. LLMS quickly creates flexible final testing evaluation report. LLMS can also integrate data from other databases. LLMS can be fully managed by the user and offers flexible and comprehensive query capabilities for test, supplier, laboratory and other information. The system can be customized to suit non-standard testing procedures and methods. It also uses non-proprietary technology to maintain its code infrastructure and database. Lyons software systems are not "hard-coded" and all content is managed and secured by the appropriate manufacturer's personnel. Easy customization to meet your business needs. Fully user-friendly and administered. Requestors can easily request product testing before the product is sent to laboratory.

QualityPro is an advanced, cloud-based Quality Management Software (QMS) designed to assist organizations in enhancing product quality, minimizing operational risks, and ensuring adherence to regulatory standards. By consolidating essential functions such as Non-Conformance, CAPA, Complaint Handling, Calibration, Inspection, Audit, Document Control, Training, Risk, and Change Management, it provides a cohesive and scalable solution within a unified platform. This integration fosters streamlined operations and supports businesses in achieving their quality objectives more effectively.

CaliberLIMS is a robust laboratory information management tool that will help you make better decisions, work more efficiently, and securely store your data. CaliberLIMS was designed to ensure regulatory compliance. It adheres to the highest standards of integrity and helps you meet all regulatory requirements. The built-in ELN, 20 plug-and-play’ modules, and many other unique features ensure that you have a faster review and more accurate analysis. This will allow for greater productivity and quality. CaliberLIMS will be your laboratory's best friend, enabling digital transformation.

Document Control is a document management system that supports controlled processes and practices in creating, reviewing, correcting and issuing documents. The QMS QISS is an ISO-based QMS QISS Software System that automates corrective action processes in regulatory environments. Your own risk-based thinking. To reduce and mitigate your risk, centralize. Standardized workflows allow you to keep track of all changes within your organization. You will enjoy many additional benefits from a paperless document management system. Establish a culture of continuous improvement and make sure that each non-conformance is visible.

AlisQI offers a highly adaptable and cloud-based Quality Management platform that is simple to implement and integrate. Our solution empowers manufacturing firms to transform their Quality Management processes into data-driven, automated, and universally accessible systems. Currently, over 70 factories around the globe utilize our platform for Quality Control, Quality Assurance, and QESH management. We assist our clients in minimizing waste by as much as 15%, enhancing their quality standards, and achieving time savings of up to 20%. Serving a diverse clientele that spans all six continents—from startups to Fortune 500 companies—we take pride in our track record of retaining every customer. Our clientele extends across various manufacturing sectors, including Chemicals, Personal Hygiene, Food & Beverage, Automotive, and General Manufacturing. With such a wide-ranging impact, we continue to innovate and support the evolving needs of our customers.

SoftExpert EQM stands out as an all-encompassing enterprise quality management software (EQMS) that aids organizations in obtaining and upholding ISO 9001 certification by automating and enhancing quality processes specifically designed for their unique products, operations, and business practices. This modular and adaptable platform integrates all essential quality initiatives, including process mapping and the management of documented information such as standard operating procedures, work instructions, and records, along with non-conformance reports, corrective and preventive actions, and quality indicators. Furthermore, the software efficiently oversees supplier relationships, addresses customer complaints, conducts quality audits, manages training and competencies, and evaluates quality risks and controls, as well as quality inspections and statistical process control, all of which contribute to a more agile and resilient quality management system. By streamlining these diverse functions, SoftExpert EQM empowers organizations to enhance their overall quality performance and compliance.

Omda ProSang is a sophisticated Laboratory Information Management System (LIMS) designed for comprehensive management of blood, cells, and tissues, ensuring complete traceability from the donor to the recipient. This system is employed in various settings, including blood donation centers, immunohematology and clinical immunology laboratories, transplantation facilities, tissue establishments, and stem cell centers. With decades of reliable support for ISBT 128, Omda ProSang is a trusted solution for over 180 blood centers across five nations. It delivers a thoroughly documented process along with full traceability, which enhances oversight of the entire donor-to-recipient journey. The automation of processes significantly streamlines testing and analysis workflows while facilitating effective communication with donors. Additionally, the platform is equipped with robust safety mechanisms aimed at enhancing patient safety, and it features comprehensive statistics and analytical tools that empower healthcare providers to optimize their resource utilization. Overall, Omda ProSang stands out as an essential tool in modern transfusion medicine.

Element LIMS stands as a versatile commercial off-the-shelf (COTS) laboratory information management system designed for laboratories engaged in testing various substances, including water, soil, air, food, and cannabis. Enhance productivity and ensure adherence to regulations through user-friendly workflows, advanced analytical features, and robust data handling capabilities. By simplifying login processes, fortifying lab analyses, automating report generation, expediting instrument data uploads, and incorporating quality control measures, this system effectively meets diverse laboratory needs. Each day, numerous users across commercial, private, federal, state, and local government labs reap the benefits of Element LIMS's extensive functionality. Tailored specifically for environmental testing laboratories, the system offers features that cater to the unique demands of soil, water, air, cannabis, and food residue analysis. Furthermore, it optimizes project management by providing project templates and facilitating the automated transformation of bids, thereby enhancing efficiency. With automated bench sheets, seamless instrument integration, and the ability to process samples in batches, Element LIMS significantly simplifies sample management for laboratories. This comprehensive approach not only boosts overall operational efficiency but also empowers labs to focus more on their core testing objectives.

Benefits of Revol LIMS: Improved Productivity - Revol LIMS automates laboratory workflows, reducing manual errors and increasing productivity. Enhanced Data Management - The system provides a centralized platform for data management, ensuring data integrity and compliance with regulatory requirements. Increased Efficiency - Revol LIMS streamlines laboratory operations, reducing turnaround times and improving overall efficiency. Better Decision-Making - The system's advanced reporting and analytics capabilities enable laboratories to make data-driven decisions. Regulatory Compliance - Revol LIMS ensures compliance with regulatory requirements, reducing the risk of non-compliance and associated penalties.

Agilent SLIMS takes charge of every aspect of your laboratory, from initial sample receipt to the generation of automated reports. By integrating the functionalities of a laboratory information management system (LIMS) and an electronic laboratory notebook (ELN), SLIMS offers comprehensive solutions that help you effectively oversee the entirety of your lab's content and context. Regardless of the intricacies of your laboratory environment, SLIMS is designed to meet your specific requirements. Its user-friendly interface allows you to monitor assets efficiently, swiftly rectify issues, and optimize your workflows. Additionally, the system can be quickly set up, which minimizes the time and effort required for implementation. Our team of SLIMS engineers possesses extensive expertise in laboratory informatics and scientific processes. They are well-versed in your domain and are committed to supporting you through various project phases, including installation, validation, and customization of the software, ensuring that it is tailored to your unique operational needs. With their assistance, you can maximize the effectiveness and efficiency of your laboratory operations.

LabPortal is an advanced Veterinary Laboratory Information System (VLIS) that automates critical laboratory tasks for faster turnaround times and reduced errors. This cloud-based solution integrates seamlessly with a variety of analyzers, allowing veterinary laboratories to manage their operations more efficiently. LabPortal features electronic lab notebooks, automated sample tracking, and inventory management to streamline processes and ensure the accuracy of results. Additionally, the system supports invoice and billing management, allowing laboratories to improve both their operational efficiency and profitability. LabPortal is designed to reduce human errors, such as sample mix-ups and contamination, by automating repetitive tasks, enabling veterinary professionals to focus on precise decision-making and patient care.

Oasis Infotech, certified with ISO 9001:2015, stands out as a prominent application development firm, specializing in industry-specific offerings within the QC/QA domain, including LIMS (Laboratory Information Management System), QMS (Quality Management Systems), and Automation Solutions aimed at enhancing the productivity and efficiency of laboratories through integrated informatics, services, and solutions. Their diverse product range incorporates cutting-edge technology and consulting services designed to automate contemporary laboratories, playing a crucial role in the creation of a broad spectrum of applications that facilitate the digitalization of manufacturing facilities, analytical and research laboratories, and other related processes. By prioritizing prompt, consistent, reliable, and cost-effective service, Oasis is dedicated to supporting its global clientele across various sectors while upholding confidentiality and integrity to aid organizations in achieving regulatory compliance, ensuring they remain competitive in an ever-evolving market. This commitment not only fosters trust but also highlights the company’s expertise in navigating complex industry standards and regulations.

KareXpert LIMS (Laboratory Information Management System), is a software program that manages, stores, and analyzes data generated in a laboratory. It aids laboratory personnel in streamlining processes, increasing efficiency, and ensuring data accuracy. LIMS functions include sample collection and dispatch, sample acknowledge, sample acknowledge, outsourced sample management, sample processing, and sample acknowledgment. It can be used in conjunction with other laboratory equipment to automate data transfer and reduce potential errors. KareXpert LIMS provides secure access controls and data tracking to improve data security and regulatory compliance.

OpenFreezer is an open-source information management platform aimed at biological laboratories, designed to streamline reagent tracking and workflow management. This system meticulously records details about each reagent used in the lab, including unique properties like sequences and external identifiers, as well as information on their physical preparations, such as storage locations and characteristics. In addition to serving as a comprehensive repository for reagent data, OpenFreezer also features workflow tools that assist with tasks like primer design and automated feature mapping, making it an essential resource for bench scientists. It offers a suite of software tools tailored to meet the needs of wetlab scientists, enhancing their efficiency and productivity. At its foundation, OpenFreezer focuses on tracking various types of reagents, their specific properties, all isolates and preparations, and the precise storage arrangements within the laboratory for each reagent prep. This holistic approach to reagent management and workflow optimization positions OpenFreezer as a crucial asset for any biological research facility.

eZLabs: the ultimate Laboratory Information System (LIS) eZLabs stands out as a premier Laboratory Management System tailored for diagnostic centers, significantly boosting productivity through the integration of top-tier technology and adherence to industry best practices. This online LIS platform can be effortlessly adopted, resulting in a coherent workflow that connects your laboratory, doctors, and patients seamlessly. Transform the operations of your lab with eZLabs, allowing you to establish unprecedented connections with both your doctors and patients. The platform enables efficient communication utilizing popular tools like WhatsApp, Email, and SMS, all accessible directly from your eZLabs account. Automated messages via WhatsApp, SMS, and Email are dispatched at various points in your workflow, covering everything from Billing to Report Dispatch. With eZLabs, you can streamline Billing, Reporting, and Printing while conducting thorough Revenue Analysis, ultimately enhancing your lab's efficiency and service delivery. Now, you have the ability to focus on what truly matters—providing excellent patient care.

By utilizing Lenava LIMS software in your laboratory, every single aspect of your operations remains meticulously managed. It offers an all-encompassing and unified perspective on samples, tests, and workflows, ensuring nothing is overlooked. Furthermore, it allows for real-time monitoring of modifications throughout the sample's lifecycle and keeps an extensive log of every action taken on it. Key features include tracking sample locations, managing inventories of reagents and consumables, integrating instruments, and facilitating the development and enhancement of workflows. Its high configurability and modularity, paired with robust report generation capabilities, empower your laboratory to exceed customer expectations. With our solution, you can actively manage sample accessioning and data handling as fundamental components of your laboratory's software suite. Additionally, you can introduce automation and streamline your processes, transforming any scientific workflow into a series of manageable and trackable steps. This ensures that your laboratory operates efficiently and effectively, consistently delivering outstanding results.

StackWave offers a state-of-the-art Laboratory Information Management System (LIMS), Electronic Laboratory Notebook (ELN), and Scientific Data Management System (SDMS) designed to enhance the efficiency of laboratory operations. With StackWave’s assistance, you can streamline labor-intensive scientific tasks, allowing your team to concentrate on critical research activities. These laboratory software solutions are adaptable and suitable for organizations of various sizes and sectors. Our systems cater to an extensive array of processes, having successfully collaborated with startups in biotechnology, major pharmaceutical firms, and everything in between. By utilizing cutting-edge web, database, and software technologies, the StackWave LIMS stands out as the most advanced laboratory information management system currently on the market. Built upon StackWave’s established software framework, the LIMS guarantees the flexibility, dependability, and performance required to tackle your most challenging information management needs, ensuring your laboratory is well-equipped for future advancements. Thus, embracing StackWave’s solutions will not only enhance your laboratory's operations but also position it for long-term success in a competitive landscape.

A comprehensive Resource Management, Business Process, and Workflow Management System designed for laboratories specializing in testing food, air, water, wastewater, sludge, soil, and noise. This Laboratory Information Management System (LIMS) is ideal for environmental testing, research institutions, and quality control labs. KRITI LIMS offers a fully web-based and highly adaptable solution tailored for testing laboratories. It oversees the complete automation of business processes and workflows within these labs. This solution efficiently manages a range of testing activities, including sample booking, tracking, quality control, research and development, test report generation, billing, accounting, and business intelligence modules. Additionally, cloud-based options are available to accommodate multiple laboratories and institutions seamlessly. Say goodbye to tedious and prolonged implementation timelines; you can configure and start running your lab in just seven working days. With KRITI LIMS, efficiency and flexibility are at your fingertips, ensuring that your lab operates smoothly and effectively.

CloudLIMS.com has been certified by ISO 9001:2015. CloudLIMS.com, a cloud-based Laboratory Information Management System (LIMS), offers strong data security, complimentary support, instrument integration and hosting, as well as data backups. This allows biorepositories, diagnostic testing, and research laboratories to manage data and automate workflows. Our mission is to empower and digitally transform laboratories around the world to improve their quality of life. We created a digital tool called Laboratory Information Management Systems, (LIMS), that manages all information and data flow for clinical and analytical laboratories. We have helped hundreds of analytical testing laboratories to keep food, air and water safe for public consumption.

The LigoLab LIS & RCM Laboratory Operating Platform™, a comprehensive enterprise-grade platform, includes modules for AP and CP, MDx and RCM. It also supports Direct-to-Consumer. This allows laboratories to be more competitive in the marketplace, scale up their operations and become more profitable. The RCM module integrates with the LIS and automates ICD/CPT coding. The billing process begins at order inception and includes verification, eligibility and scrubbing components. This increases claim submissions and revenue and decreases claim denials. TestDirectly is a portal for patient engagement that allows labs and collection facilities scale collection, testing, reporting, and reporting workflows. This reduces friction and eliminates errors that can be caused by manual labor and paper forms.

FactoryQA is a quality management software that can be used by manufacturers. Software Features 1. Management of Non-Conformance/CAPA 2. Document Control 3. Instructions for Work 4. Inspection sheets 5. Audits 6. Analytics Services: 1. ISO Certification Consultants 2. Workshops for ISO Certification 3. Fractional Quality Management Services

A clinical information and data management system enables laboratories to achieve optimal performance and enhance patient care through standardized workflows and streamlined processes. This lab automation software oversees staff management, reporting, inventory control, and essential tasks, effectively handling the vast amounts of data generated by many laboratories. Despite the benefits, overseeing laboratory information can be difficult, leading to potential downtimes, errors, and even financial losses due to equipment failures. Fortunately, there are software solutions designed specifically to tackle these challenges. Such solutions come equipped with a variety of features that significantly enhance workflow efficiency and laboratory operations. As a prominent player in the life sciences sector, Medical Laboratory Software (SumLims) provides robust tools that help laboratories manage their data efficiently, ultimately saving time and increasing productivity. By utilizing these advanced functionalities, labs can focus more on their core objectives and improve overall service quality to patients.

Confience myLIMS is an advanced Laboratory Information Management System (LIMS) that simplifies lab operations across industries like water, food, manufacturing, and automotive. This all-in-one software helps labs manage samples, automate workflows, and ensure data accuracy while staying compliant with standards like FDA 21 CFR Part 11, ISO 17025, and GLP/GMP. By optimizing processes from sample collection to reporting, Confience myLIMS ensures labs meet regulations and deliver top-quality results. Key features of myLIMS include intuitive dashboards that provide real-time insights into laboratory operations, enabling users to monitor performance metrics and make informed decisions. The software also offers seamless integrations with existing laboratory instruments and systems, allowing for a cohesive workflow that minimizes manual data entry and reduces the risk of errors. Confience myLIMS stands out by automating routine tasks and offering a central platform for data management, allowing labs to enhance analytical capabilities and improve turnaround times. Additionally, myLIMS includes powerful reporting tools that enable laboratories to generate comprehensive reports effortlessly, supporting data analysis and compliance documentation. One of the standout benefits of myLIMS is its ability to drive continuous improvement within laboratory environments. By automating routine tasks and providing a centralized platform for data management, laboratories can focus on enhancing their analytical capabilities and improving turnaround times. This not only leads to faster results but also fosters a culture of quality and accountability, which is essential in today’s competitive landscape.

Clarity LIMS serves as a sophisticated laboratory information management system specifically tailored for genomics laboratories to effectively monitor samples and streamline workflows for enhanced laboratory efficiency. Beyond mere sample tracking, Clarity LIMS acts as a vital digital infrastructure for laboratory operations, encompassing every aspect from data and sample management to the oversight of personnel, equipment, and supplies. By standardizing and automating workflows, it significantly reduces the time required for processes and minimizes the likelihood of human error. This platform is designed to grow with your laboratory's needs, easily integrating new technologies and methodologies. Clarity LIMS also facilitates quicker laboratory operations through its easy-to-use implementation, offering preconfigured workflows for Illumina sample and library preparation kits, alongside quality control mechanisms that identify subpar samples. In addition, it aids in maintaining compliance with features such as electronic signatures, audit trails, reagent tracking, and robust privacy and security measures. Lastly, Clarity LIMS enhances precision through automation, incorporating built-in business logic and error-checking systems to ensure reliable results.