Alternatives to Nova-QMS

A cloud LIMS that tracks samples, tests results, and manages inventory for life science research, industrial QC labs, and biotech/NGS. Includes regulatory support for CLIA and HIPAA, Part 11 and ISO 17025. The quality, security, traceability, and traceability for samples is crucial to a lab's success. Laboratory professionals can use the Lockbox LIMS system to manage their samples. They have full visibility of every step of the sample's journey from accession to long-term storage. LIMS analysis is more than just tracking results. Lockbox's multilayered sample storage and location management functionality lets you define your lab's storage structure using a variety location options: rooms and storage units, shelves and racks, boxes and boxes.

QBench allows you to keep track of all your samples and where they are located in the workflow using a single system. QBench eliminates the need for spreadsheets, shared folders in the network, and paper-based tracking systems. You can view hundreds of PDF reports/COAs before publishing or emailing. You can generate barcodes and create labels that you can customize for your samples. Compatible with standard printers and scanners. QBench's billing module allows you to create and send invoices right from the system. You can see counts and latencies for different data types in QBench. This includes metrics like turnaround time, sample counts per test, sample delay, and many others. QBench makes it easy for you to gather the data your lab needs for the assays you perform.

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.

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.

Unify quality processes with QT9's all-in-one cloud-based QMS Software Suite. QT9 QMS is a user-friendly quality management software that includes 25+ modules with unlimited scalability. Automate ISO & FDA Compliance with email alerts, To Do lists and FDA 21 CFR Part 11 Compliant Electronic Approvals. QT9 QMS enables Life Sciences, Biotechnology Companies, Medical Device Manufacturers and Pharmaceutical Companies to digitally transform operations. Get real-time status updates and visualize quality metrics up-to-the-minute. QT9 QMS comes with built-in document control, revision-level controls, corrective actions (CAPAs), Nonconforming products and more. Advance product releases with Deviation Management, Engineering Change Orders, FMEA, Inspection Management Modules Included. Go paperless & put time-consuming tasks on autopilot. QT9 QMS comes ready-to-use. Get a free product tour! Start a Free Trial. Visit QT9qms.com

Qualityze EQMS Suite is a next-generation Enterprise Quality Management Software. It is specifically designed for businesses to efficiently manage their quality processes, customer expectations and compliance requirements. It helps them address operational challenges so they can achieve excellence in terms of quality, safety and reliability. It comes with pre-defined templates for controlled documents, audit checklists, regulatory forms, material compliance reports and many more. Qualityze EQMS Suite is a set of 14 integrated modules that help create a closed-loop system to manage end-to-end quality from anywhere. Our range of smarter quality solutions is built on the Salesforce.com technology platform. These modules are Nonconformance Management, CAPA Management, Document Management, Change Management, Audit Management, Training Management, Supplier Quality Management, Inspection Management, Customer Complaints Management, Material Compliance Management, Forms Management, Permit Management, Calibration Management, and Maintenance Management, Forms Management and Field Safety Management. Our Quality Management solutions help create a culture of quality and continuous improvements by proactively mitigating quality issues.

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.

Natively built and operated on the Salesforce platform, QHSE is the fastest growing Enterprise Quality, Health and Safety Management System. Unified QHSE solutions combine EQMS with EHS to help customers of all sizes deliver high quality products and services in a safe and sustainable manner. They reduce risk, inefficiencies, and inefficiencies, while protecting their customers, employees, and brand.

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

Intellect's QMS software has been proven to improve quality operations and reduce overall quality cost by up to 40%. Our apps were designed by certified quality professionals and can be easily customized with our no-code platform or drag-and-drop technology. Remote access for your team, mobile apps, dynamic workflows, analytics, reporting, and remote access are all possible with this modern and simple solution. Apps include Document Control and Employee Training, Audit Management CAPA, Nonconformance, as well as other useful features.

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.

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.

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.

Revolutionize your Life Sciences processes. You can dramatically improve the quality, control, and efficiency of your products and processes. Our fully compliant platform is pre-validated according GAMP5. This ensures inspection readiness at all time. You have complete control over all documents and processes. You can also customize workflows and automate when possible. You can enjoy uninterrupted workflows and full traceability with seamlessly connected and integrated modules. Our dedicated team is available to answer any questions you may have. Only the best Scilife experience is possible! Our Scilife platform automates, automates and organizes all processes in your industry space, no matter if you're in Medical Devices or Pharma & Biotech or ATMP. Click below to see which Scilife modules are available for your industry's unique lifecycle stages.

Loftware Prisym 360 offers innovative content management features that incorporate industry best practices. It is specifically designed to meet the complex regulatory requirements for clinical supplies labeling. Many clinical labeling teams use English MLT/CLT variants for defining the content of booklets and labels for clinical trials. The number of countries in each study increases and each country has specific regulatory content, phrases, and language requirements. Therefore, the manual process of designing booklets and printing them takes longer and is more risky. Prisym 360's CLT/MLT solution prompts users to provide study information. Then, it automatically generates MLT, CLT, and booklet designs based on its knowledge about content and design requirements. This reduces the time it takes to create a clinical label or booklet, reduces errors and ensures compliance with regulatory requirements.

Pharmaceutical and Biotech companies face challenges in meeting control documentation requirements in their day-to-day operations. Document management and control are essential components of any quality and compliance solution. Global Regulatory agencies expect all regulated companies to follow industry best practices during the manufacturing process. Phama Soft Sol created Document Management System software to help manage and distribute SOP's, STP's, and other regulated documents. Document management software systems can not only lower compliance costs but also improve product quality and process efficiency. Document Management System (softDMS) allows you to quickly retrieve the information you need, at the exact time you need it. This reduces the risk of miscommunications and errors which in turn minimizes risks, manhours, and other documentation errors.

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.

Ennov Quality Suite. A comprehensive QMS to increase efficiency and ensure compliance. Ennov Quality Suite Ennov Quality Suite combines the power of Ennov Doc and Ennov QMS with Ennov Report and Ennov Training to create an integrated quality management solution that improves operational efficiency and ensures compliance to industry standards like 21 CFR Part 11, GxP, and ISO. Ennov Quality offers a predefined inventory that includes quality documentation, processes, and workflows. These are based on industry standards and best practices. Ennov Quality customers can quickly get their system in production and begin to realize their return on investment. Ennov Quality, as all Ennov solutions, is easy to set up and requires no IT skills. A unified and intuitive content and information management platform that supports and enriches the entire Life Sciences product cycle. Our comprehensive QMS improves operational efficiency

Paradigm 3 is both a web- and desktop-based platform that helps businesses manage compliance in document control, CAPA compliance, Competency Tracking, Training, and Document Control. The software includes tools such as an event manager to handle customer complaints and incident investigations, as well as tasks sent by e-mail and audit preparations. Paradigm 3 is beneficial to the following industries: Manufacturing, Test Labs, Healthcare, and Service Industries.

ZenQMS improves the quality compliance profiles life sciences companies through a cloud-based platform. It is purpose-built to facilitate document collaboration, control, training, issues management, audits, and change management. ZenQMS is a team of technology and quality leaders who share the common goal of making quality management a business imperative.

Software that helps you comply with regulations. Fannie Mae, Wendy's and Walmart trust the best mobile inspection and audit platform. This will help you improve safety and accuracy. The #1 field management platform for teams, FORM OpX will transform your Excel, paper, and digital processes. FORM OpX combines advanced data gathering and configurable workflows with powerful operational insight to increase compliance in real time. To ensure compliance and team compliance, you can set up audits, inspections, or workflows. Digital forms allow you to capture data and guide teams to the right actions. Set up automated alerts and escalates to prompt corrective action when issues arise. You can save time and money by creating customizable workflows that improve processes, increase compliance, and reduce errors.

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.

BatchMaster Manufacturing ERP Solutions can be used by formula-based process manufacturers in the Food, Chemical, Nutraceutical, and Life Sciences industries. Our software supports batch production, formulation, packaging management, batch production, quality and recall, lot traceability & rappel, industry-specific compliance, planning, scheduling, mobile warehousing, and other process manufacturing functions. Manufacturers can use their existing financial systems to run our process manufacturing application, including QuickBooks, Sage 100&300 and Microsoft Dynamics GP. We offer an ERP solution for manufacturers looking to replace or upgrade existing business systems. It supports specific manufacturing, financials and sales as well as supply chain, purchasing and customer service. Our applications are available on-premise (purchased), and in the cloud (monthly subscription programs).

InstantGMP™, which replaces multiple software and/or paper-based solutions for managing your manufacturing and compliance needs, could be the key to unlocking your business's full potential. With a single, affordable software solution, you can easily increase production uptime, improve batch quality, and meet all FDA compliance requirements. InstantGMP™, which can be used individually or together depending on your business needs, delivers comprehensive, integrated software solutions that ensure quality, consistency, and GMP compliance. We will help you choose the right solution for your business today and tomorrow. You can organize, manage, and document batches electronically while promoting good manufacturing practices. Inventory Management Software that meets Part 11 requirements and GMP requirements. A complete quality system with templates, SOPs and guided workflows that is ideal for virtual biotech.

SoftExpert EQM (enterprise quality management software) is the most comprehensive. It assists companies in achieving and maintaining ISO 9001 certification by automating highly interactive quality processes that are tailored to their specific products, operations, and business practices. As a modular and scalable solution platform, SoftExpert Quality Management Software seamlessly integrates all key quality initiatives, including process mapping, documented information (SOP - standard operating procedures, work instructions and records), non-conformance reports (NCR/NCMR), corrective/preventive actions (CAPA), quality indicators (KPIs). The solution can also manage supplier relations, customer complaints and quality audits, as well as competence and training, quality controls, quality inspection, and statistical process control, increasing QMS flexibility and robustness.

Quality Collaboration By Design (QCBD), a fully integrated quality management solution, is designed for manufacturing businesses. This Windows-based, affordable application makes it easier to achieve and maintain compliance with quality management standards like ISO 13485 and ISO 9001. CAMA Software's QCBD module offers a variety of modules for supplier management, training management, process deviations management, document control, equipment and more.

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.

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.

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.

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.

CSols AqcTools™ v2.6 allows users dynamically display Analytical Quality Control Charts (AQC) charts to monitor laboratory performance. It provides paper-free auditable investigations of control limit violations, comprehensive reports, and reduces time spent assessing and processing your QC data. AqcTools will be of benefit to customers in the water, environmental, and public health sectors as well as industrial laboratories that perform chemical, clinical, and microbiological analyses. AqcTools offers a variety of interactive, dynamic charts, ranging from the standard individual plotted AQC points to charts that can use both batch and daily data. To support ongoing analyst competency testing, users can also plot charts for individual analysts. You can view all information about each point, including date, batch number and analyst. All this information is just a mouse click away.

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.

Cloud-first ERP is specifically designed for life science organizations. Merit for Life Science, a cloud-first ERP, is specifically designed for biotech, pharmaceutical, and medical device manufacturers. It connects your entire organization with Dynamics 365 finance operations and finance. Mapping production requirements and resource qualifications. Monitoring vendor relationships in procurement to ensure manufacturing meets quality standards. Transparency and visibility for your life science organization to ensure safe and innovative products. We understand that every organization has its own unique needs. Get a complete overview of our services. We deliver a custom-tailored solution to meet the needs of pharma, biotech, medical device, and other companies. Using reliable, auditable accounting practices will improve your decision-making. Set financial reporting standards for acquired entities and prepare for acquisition.

A well-implemented Quality Management System (QMS) is essential for biotech firms to achieve regulatory compliance. It will also help them maintain product quality and safety. It will also help them manage risks effectively. It will drive operational efficiency. InstantGMP QMS was designed by quality and regulatory professionals for biotech companies. It is simple, affordable, and complete. It can be used by small-to mid-sized manufacturers in many different industries. This quality management software features guided workflows to reinforce adherence with government standards during the entire production process. It also has a variety of innovative features and specialized module. Maintain and improve the safety and quality of biotech products. Frameworks are provided for identifying, assessing and mitigating risk throughout the product's lifecycle to reduce the likelihood of quality incidents or product recalls.

UniPoint's Quality Management Software can be used on-premise to manage quality. Quality Management Software is easy to integrate with other ERP systems. Quality Management Software can be used by manufacturers of any product, in any manufacturing mode. With Quality Management Software, users can manage processes such as document control, equipment management, non-conformances, corrective/prevantative actions, and more.

Software that allows you to track and organize Quality Risk Management information online. It uses web-based technology to trace Quality information to the specific risk it poses to the patient or drug product. Why Choose Us? CINCO is a risk-based software for quality management in the Life Sciences Industry. It allows transparent quality decisions by allowing for paperless traceability of all critical quality aspects of a drug or medical device. Why Risk Management? Quality Risk Management is a method that identifies and mitigates the risks associated with a drug or medical device manufacturing operation. Most regulatory agencies require it. The paper-based approach used by the Life Sciences Industry is ineffective in managing significant and valuable risk data. It is susceptible to errors, introduces too many friction to users, and does not add any value to the operations. Access to the most critical information about the product on-demand

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.

1factory's Manufacturing Quality software is cloud-based and on-premises and was specifically designed for manufacturing companies of any size. 1factory's Manufacturing Quality is a reliable and secure solution that allows for first article inspections and factory monitoring. It also provides quality control plans, in process and final inspections, inspection management, CAPAs and non-conformances. Other key features include the ability to calculate Process Performance (Ppt, Ppk), and Process Capability (Cpt, Cpk), variation/SPC control management, defect risk monitoring, and many more.

Honeywell TrackWise Digital® is a cloud-based Quality Management System (QMS) designed to streamline and enhance quality and compliance processes for businesses. With decades of expertise behind it, the platform offers robust modules for managing critical functions like document control, training programs, and corrective and preventive actions (CAPA). Utilizing advanced technologies such as artificial intelligence and machine learning, TrackWise Digital® delivers real-time insights to help organizations identify and address quality issues proactively. Its modular, flexible design ensures smooth integration with existing enterprise systems, enabling quick deployment and easy scalability. By optimizing quality operations and ensuring regulatory compliance, TrackWise Digital® supports organizations in accelerating product delivery while reducing operational risks.

Software for quality management. We offer QM solutions for all quality issues. This is what we have been doing for over 25 years. Our modular software BabtecQ is a complete solution to quality management. We are quality specialists. Babtec Qube is a cloud-based platform that allows you to connect with suppliers and customers to manage your quality tasks. Our products enable you to show the entire range of quality processes within and between companies. This is quality you will love sharing.

ACE Essentials is the pre-validated Electronic Quality Management System Software (EQMS) designed for highly regulated industries. ACE Essentials includes 10 workflows, as well as all the required Standard Operating Procedures (SOPs) and Policies. This ensures that your quality management system is fully compliant from the start. ACE Essentials features include a complete audit trail that tracks every action within the system. This allows you to understand the risks associated assets. Features of ACE Essentials Pre-Configured Workflows Pre-Configured Event Management (Due dates, Scheduling, Reminders) - Pre-Configured Permission Based Security - Pre-Configured Full Documentation - 50+ documents - Multiple Site Capability - No Charge Upgrades for the Product's Life Pre-Configured Tasks Liste - No Validation Period Pre-Configured In System Notifications Pre-Configured Email Notifications

qmsWrapper is an interconnected Quality Management Software for startups and small businesses. It helps all companies that want to increase productivity with ISO 9001:2015 and MedDev creators to easily achieve and manage ISO 13485:2016 and 21 CFR 820. Best For 1. For companies who need guidance to implement and adopt validated QMS. 2. For companies who want to automate their quality management and go beyond a paper-based system.

BIOVIA solutions provide a unique scientific management environment that enables science-based organizations to create and connect biological and chemical innovations that will improve our lives. The BIOVIA portfolio, which is a leader in the industry, focuses on integrating science, experimental processes, and information requirements from all aspects of research, development, quality control, and manufacturing. Capabilities in the areas of Scientific Informatics and Molecular Modeling/Simulation Data Science, Laboratory Informatics Formulation Design, BioPharma Quality & Compliance, Manufacturing Analytics, and Laboratory Informatics. BIOVIA is committed in accelerating innovation, improving productivity, quality and compliance, reducing cost, and accelerating product development for customers across multiple industries. Connect scientific innovation processes and information throughout the product lifecycle.

EzyPro Adaptive Management system QHSE (QHSE) enables you to seamlessly integrate compliance, performance and continuous improvement. EzyPro QHSE is a one-stop solution for compliance, maintenance and operational control. You can increase efficiency, share information, collaborate, and increase productivity. Flexible subscriptions are possible with its modular approach. EzyPro Healthcare – Hospital Quality Management System with integrated action tracking, dashboards and dashboards to meet requirements such as NABH or JCI. As a central hub for continuous improvement across the Healthcare unit, it was designed. Remote consultancy service is available for implementation support. QHSE Management System bundled comprehensive maintenance management solution. Increase equipment lifespan, increase time efficiency, and equipment uptime. This will result in lower costs and higher profits. You can easily manage work orders for repairs or maintenance, as well as transfer of assets, using a QR code assisted asset retrieval.

DataMetrics is able to provide all product manufacturers with the real-time SPC data and analytics that they require to evaluate current processes and develop a proactive approach to meet or exceed production goals, maintain or improve product quality, reduce scrap and rework costs, comply with industry standards and OEM requirements. The genius interface that connects to your entire manufacturing floor allows for universal data collection from manual, semi-automated and automated data acquisition. This allows you to collect all of your quality data in one central repository or database, and then report on it. Data silos can be eliminated by consolidating data from hundreds gages, sensors and CMM, as well as PLCs. DataMetrics, which is compliant with OPC UA, offers a solution that is backed by strict access control and advanced security.

EXTEDOpulse, a comprehensive RIM software solution, consists of five hubs that address all stages of product development. You can use the applications separately or combine them to get additional value based on your needs. The development of pharmaceutical products can be complex and require input from many people. Life science organizations face many challenges due to the complexity of operating in a highly regulated industry. We are able to provide you with great synergy and connection, as well as innovation, for compliance. EXTEDOpulse was designed with these aspects in view to help you connect the dots throughout the entire lifecycle pharmaceutical products. EXTEDO is familiar with the complexities involved in the regulatory pharmaceutical product journey.

AmpleLogic's Quality Management Software is designed to meet the strict requirements of industries that are heavily regulated. The ISO 9001-certified cloud-based Quality Management System is ideal for Lifesciences and other industries such as Food & Beverages, Cosmetics, Medical Devices or Gene Therapy. Businesses are adopting QMS solutions as they recognize the challenges of manual quality checks, which can be laborious and prone to errors. These systems are crucial in improving audit quality by automating processes, managing data efficiently, and integrating APIs.

Novatek International provides software solutions that meet or exceed the compliance and quality requirements of the life science industry. The process specific offerings provide an integrated platform that allows for consistency and standardization across multiple departments within a single site and across multiple sites.

Infor PLM Process (Optiva®,) is a product view that provides a single view of all data and processes across an organization. It is specifically designed for life science, food, and beverage manufacturers. It allows manufacturers to easily comply with regulatory and labeling requirements. This includes meeting reporting requirements, complying under labeling laws, and supplying ingredient details. Project management capabilities allow the right people to have full visibility into project data, from concept to final sign-off. Reckitt Benckiser (RB), a multinational British consumer goods company, uses modern PLM capabilities with Infor(r] PLM for Process to increase global safety and compliance. It also gets one version of the truth about its products from development to manufacturing. Integration capabilities with ERP systems allows for better insight into costs.

We offer solutions to companies that have a high standard of quality. Our software solutions are characterized by a modern UX and useful functionality. They also feature high modularity and consistent compliance. Integrated solutions to manage quality and ensure quality. Focused on digitizing controlled documents and QA process. Solutions designed specifically to meet the requirements of the financial sector for written rules of procedure and management of policies. Cloud-based, prevalidated solution for automating your validation processes as well as digitally controlling and managing validation documents. Early setup of a digital quality management system with a solution that is tailored for startups and young businesses. Based on DHC VISION. It is ready to use, with immediate compliance. No license fees. Together, we digitize the quality management and quality control processes and ensure regulatory compliance.