Alternatives to eCADinfo

RegDesk is the most comprehensive AI-enabled RIMS platform for Medical Devices, Pharmaceuticals, and IVD companies. • Our proprietary Regulatory Intelligence for over 120+ countries is translated and accessible in a standard format. In addition, it provides alerts on evolving regulatory changes • Our AI-powered Application Builder allows RA teams to prepare and publish global applications in 1/10th of the time • Our Change Assessment capability helps RA teams understand the impact of the change(s) on an existing product(s) and the action required • Our Distributor Collaboration provides seamless workflow solutions to interact, communicate, and share documents with external business partners • Our Standards Management makes it easy for RA teams to search and manage not only international but also country-specific standards • Our Tracking & Reporting functionality allows teams to track regulatory projects across the globe, receive renewal notifications, and generate reports on KPIs within seconds For more information, visit our website.

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.

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.

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.

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.

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.

ICyte is used by life science organizations of all sizes and complexity to facilitate pharma market access and commercialization. ICyte offers biotech and pharma companies world-class channel, patient and pricing data aggregation, contracts, pricing managed services and gross-to-net forecasting, accrual systems, expert launch and pricing transparency solutions, and pricing managed service contracts. ICyte helps pharmaceutical and biotech companies increase market access by quickly transforming channel, payer, complex transaction and patient data into actionable insights. ICyte also supports analytics-as-a-service, which allows common models and metrics to be deployed as a centralized service across applications, data, and analytics uses. The platform includes key performance indicators (KPIs), which are specific to Life Sciences companies. Also included are advanced analytics such as forecasting, scenario modeling, and a machine-learning-powered recommendation engine.

ChemOffice improves scientists' productivity and helps them do better research by allowing them to organize and explore chemical reactions and their properties. This allows them to turn data into actionable information and make more confident decisions. ChemDraw Excel adds chemical intelligence to Excel spreadsheets. Chemists can use Excel's sorting, organization and analysis tools to further manipulate and enrich sets and data as well as explore structure-activity relationships. Chem3D creates 3D models that allow chemists to view their compounds in three dimensions. This allows them to evaluate shape and properties to maximize specificity or activity. ChemFinder is a chemically-intelligent personal database system that scientists use to organize their compounds and to search for and correlate structures with properties.

Synergistix is focused on providing superior CRM solutions for Life Sciences businesses. Our customer relationship management (CRM), solution includes flexible software, end to end analysis services, and 100% support/help/support. This allows you to maximize the value of CRM and minimize the cost of ownership. We are proud to provide the industry with a powerful CRM solution for life sciences. The CATS Software Suite expertly combines field-based information capture with dynamic management reports to deliver state-of the-art, PDMA compliant CRM solutions for automating and managing sales force activity. Other CRM solution providers charge only for the software they offer. Life Sciences companies are left with the responsibility of planning, implementing, supporting and maintaining the systems.

End-to-end regulatory information management from a single platform. The Vault RIM Suite streamlines global regulatory process on a single cloud-based platform. This allows life sciences companies to increase visibility, data quality, agility, and efficiency. You can respond faster to changes in regulations and improve process efficiency, from submission planning to publication. Coordinate regulatory efforts across HQ and affiliates within a single RIM platform. Assure that teams are creating reliable regulatory content with high data integrity. Veeva Vault Registrations manages product data worldwide, including variations, registration status, and interactions with health authorities. Veeva's flexible data structure supports IDMP data points, and will continue to support changing regulatory data standards. Veeva Vault Submissions automates regulatory process steps and streamlines submission planning.

OpenText™, a leading provider of information management solutions for life sciences organizations, helps them to harness insights from data and content to improve their decision-making and accelerate product development. Integrate, manage and securely exchange data between people, systems, and things. Use information assets to drive innovation and commercialization. Cloud-native software can run anywhere, giving you freedom of choice. OpenText for life sciences accelerates discovery by delivering actionable insights that can be used to drive innovation in pipelines. Intelligent capture allows you to capture and manage research papers in electronic lab notebooks. Text mining can help you gain insights. Unstructured text in clinical trial reports, study protocol, clinical safety and efficiency findings, can be used to extract knowledge. Learn how to intelligently analyze and classify clinical trial documents and extract them to reduce the risk for costly stops and starts.

Platforce CRM, a cloud-based CRM that automates industry-specific business processes and improves customer engagement, is a closed-loop marketing and customer relationship management solution for pharmaceutical and life sciences companies. The system allows you to manage all aspects of marketing and sales activities, from the marketing cycle creation through territories assignment, databases creation, calls carrying, and KPI analysis.

SANeForce offers a comprehensive CRM and sales force automation solution, primarily tailored for the pharmaceutical, healthcare and life sciences industries. SANeForce is designed to increase the productivity of marketing and sales teams. It offers features such as real-time order tracking, expense tracking, stock control, and territory administration. The platform supports medical representative reporting, allowing field sales personnel log visits, capture doctor interaction, and manage appointment directly from their mobile device. SANeForce's data-driven insights, analytics, and customer engagement strategies help organizations track performance, streamline their processes, and optimize their customer engagement strategies. The solution also includes features for compliance, making it an ideal choice for highly-regulated sectors that require meticulous records and adherence to standards.

The regulatory affairs departments in the healthcare and life science industry are driven to improve efficiency and create intelligent systems that optimize costs, maximize accuracy, and reduce submission times. RIMTrack, a cloud-ready, artificial intelligence (AI)-based, new age regulatory information management system, addresses this concern. It was created from scratch to assist organizations in preparing submissions accurately and efficiently. It streamlines regulatory processes related to licensing, approvals, regulatory, competitive intelligence, clinical trials and reporting across global stakeholders. Integrate with existing RIM systems to achieve complete management of the regulatory lifecycle process.

Glemser offers IT solutions for regulated sectors with a focus in global life sciences and the ecosystem that enhances patient outcomes. ComplianceAuthor makes it easy for life science companies worldwide to manage product labeling, provide affordable IDMP, and reduce compliance risk. ComplianceAuthor for Global Labeling assists life science regulatory professionals to manage, scale, simplify, and streamline global product labels and compliance through artificial intelligence and structured content and natural language generation. Artificial intelligence and machine-learning are used to determine, index and derive the knowledge required to recommend the best course of action.

Montrium is a knowledge-based business that uses its deep understanding of GxP technologies and processes to provide cost-effective solutions for life science organizations. Montrium Connect, the industry-leading platform for managing regulatory content, processes, and compliance in life sciences, has been designed to meet the needs of the new pharmaceutical business model. Users can collaborate and find the information they need faster and easier with intuitive navigation, enhanced user experience and dynamic content management.

FactoryTalk®, PharmaSuite is a leading MES solution designed specifically for the Life Sciences sector. It optimizes each stage of the recipe cycle based on roles and speeds up results for all users. Its open-content architecture combined with an intelligent upgrade engine makes it a powerful system for growing in batch and discrete processing. FactoryTalk PharmaSuite MES offers value-based applications that help you comply with regulatory compliance guidelines. MES can help you achieve operational excellence, improve the effectiveness of your supply chains, and meet your sustainability objectives. PharmaSuite MES offers production operations management to help meet regulatory compliance, achieve operational excellence and increase supply chain effectiveness. Modern MES allows you to optimize production, speed time-to market, and ensure compliance.

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

All researchers from different industries can use the same environment! ResearchManager is a platform that allows researchers to access all functions and information from one place. They can also share it with others. This platform is for researchers who are ready for the future. Future where patient and data access and sharing are central. We provide support for everyone involved in research in the life sciences sector. This is done through an online platform that includes the eClinical tools EDC and CTMS & ERMS. This allows researchers to share data and facilitates research at a higher level. We are also experts in the fields of data validation, enrichment, and collection.

GHSAuth by Mar-Kov Computer Systems, a robust Global Harmonized Standard compliant Safety Data Sheets (SDSs) and Safety Label authoring software for chemical manufacturers, is available. GHSAuth allows EH&S staff to manage and organize SDS files for their organization, access a list of hazard codes, precautionary phrases, track changes and achieve revision control. You can choose from both a free and a paid version of the software package.

Unstructured health data can be unified and liberated with Interactive AI and NLP solutions that deliver health insights to Providers. Payers. Life Sciences. Interactive AI and NLP solution to unlock healthcare insights from unstructured clinical data. Provider. Accelerate data abstraction and clinical validation of clinical notes information. Reduce time and costs needed to identify care gaps, review care quality dashboards and create registry reports. Payer. To better manage high-risk and high-cost member cohorts, integrate and analyze claims data and clinical notes. Life Sciences. Use clinical trial databases and data taken from clinical notes to quickly match patients with clinical trials. Real world clinical data and evidence can be leveraged. Ember is a complete solution that combines NLP and predictive analytics. Streamline. Healthcare Analytics for Unstructured Data to Improve Quality and Efficiency.

A platform that connects scientific reasoning, compound design, computational resources, and other relevant information. The Design Hub by Chemaxon for medicinal chemistry, from analysis to prioritization. One platform to design compounds and manage ideas. One platform that links scientific rationale, compound design, computational resources, and other information. You can switch from PowerPoint files to graphical or chemically searchable hypotheses, which are integral parts of compound design. You can easily work in a rich visual environment with your trusted physchem properties, computational models or novelty issues. This secure online service allows you to involve your CROs in compound progression. Analyze the evidence from biological assays and experimental structural information to extract SAR and create new hypotheses for each optimization iteration. Your scientific hypotheses can be stored in a "designer’s ELN" (chemically-aware drawing canvases).

Kalypso offers life sciences companies a cost-effective accelerator to implement a RIM system - Accel for RIM. The integrated platform allows for efficient product distribution and management, as well as a global platform to track and manage product registrations. It consolidates compliance data and quality data from different enterprise solutions into one global source of truth to facilitate product registrations and tracking in order to speed up regulatory submissions. Modern APIs are used to combine product data, regulatory documentation, and submission packages. Pre-configured for quick implementation with a valid software system. Based on industry-leading RIM practices.

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

Transform your way of managing bids and tenders. Move processes and data from disparate spreadsheets to one platform. XS Suite has you covered ensuring maximum ROI on every tender with hundreds of out-of-the-box functionalities. eXtensibility is a concept that allows for a wider range of options and functionalities. It connects all stakeholders in the tendering process to ensure everyone is aligned on the main objectives and goals. A one-stop solution that addresses all the needs of a tender office representative. Managerial business tool to monitor performance, including contract compliance and business development over many years. You can monitor your tender life cycle in real time and use advanced analytical tools for insights to gain an edge over your competitors. Quickly and easily generate reports that track the Company's business bid and tender activities.

Azenta Life Sciences provides scalable, flexible, and powerful informatics sample processing systems that allow lab systems to efficiently deploy across all locations and use built-in project management functionality. We offer unrivaled sample exploration, management, and delivery solutions to accelerate discovery, development and delivery. Azenta Life Sciences offers cloud-based informationatics solutions for sample processing. These solutions automate laboratory workflows, and reduce staff workloads through standard processes. Modules can be used to manage patients, families, clinical trials, informed consent, storage and diagnostics, as well as sample processing. Interfaces with external data sources are available and flexible options for integrating 3rd-party systems and instruments.

The enterprise content gap can be bridged to achieve global harmonization and local autonomy. Veeva Vault, a cloud-based enterprise content management platform that includes a suite of applications designed for life sciences, is a true cloud enterprise solution. Companies have traditionally had to deploy separate applications to manage data and content applications. Veeva Vault is a content management platform that can manage both data and content. Companies can now eliminate site, country, and system silos and streamline all aspects of commercial, medical, clinical and regulatory quality and safety. All Vault applications are built from the same core platform. This allows companies to gain efficiency and compliance by allowing for a seamless flow of documents between regions and departments. The content is always available, current, and in context throughout the entire development and commercial lifecycle.

Cognidox is an online document-management system for high-tech, life sciences and medical device product development. Cognidox is available in the cloud and as an on-premise solution. It promotes product lifecycle management and knowledge sharing between developers and clients, partners, customers, and customers. Cognidox is secure and reliable. We offer plug-ins for many programs, such as Microsoft Office. We also offer an API that allows you to integrate almost any process with Cognidox. Cognidox's core function is a DMS. An add-on for Cognidox allows you to license and distribute documents to third parties via a fully sandboxed website. This allows you to publish specific documents while keeping your main storage secure. Another popular add-on is gBMS - Graphical Business Management System. Visio can be used to capture your business processes. A good BMS should give clear oversight of your entire operation.

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.

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.

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.

Datatrak International, Inc. is a software-as-a-service provider of enterprise cloud-based technologies for the life sciences industry. Datatrak's unified eClinical solution and related services improve efficiency and cost effectiveness for the clinical trial industry. Datatrak developed its multi-component, comprehensive solution using a single platform. This concept was expanded to include services delivery through Datatrak's Clinical and Consulting Services groups. The Company offers a complete range of software products that can be used to speed up the reporting of clinical research data to sponsors and regulators. This is faster than using loosely integrated technologies. Our goal is to empower workgroups with role-based access, version-controlled file management and calendar events, tasks, and contacts. All built within our eClinical software applications, including EDC, CTMS and reporting.

Global life sciences industry trusts us to drive intelligent engagement. Intelligent HCP engagement across all channels in real-time can improve customer experience. Data science and embedded intelligence can be used to provide customers with the most relevant and effective messages. Field teams should have access to the most current information and insights in order to plan and execute calls. Compliant note capture can help you build deeper customer relationships. Pre-built and custom visualizations provide tailored insights at the point where execution takes place. Veeva CRM allows commercial organizations to use artificial intelligence in the way they choose. Veeva CRM Suggestions is an open model that allows you to implement the best actions with any data science provider.

Accelerate scientific discovery, empower your R&D team and use harmonized data in cloud to accelerate your R&D. The Tetra R&D Data Cloud is the only cloud-native data platform for global pharmaceutical companies. It combines the power of the largest Life Sciences integrations network and deep domain knowledge to provide a future-proof solution to harness the power of your most important asset, R&D data. The cloud covers the entire life-cycle of your R&D data: from acquisition, harmonization, engineering, downstream analysis, and native support for state–of-the–art data science tools. Pre-built integrations allow for easy connection to instruments, informatics and analytics applications, ELN/LIMSs, CRO/CDMOs, and other vendors. Data acquisition, management, harmonization, integration/engineering and data science enablement in one single platform.

Aktana uses embedded artificial intelligence, which is refined by real-time human insights, to give life sciences sales and marketing professionals the information they need in order to improve customer experience. Aktana's AI-driven next best-action platform integrates seamlessly with every data source and player in your commercial tech stack. This transforms mountains of data into clear recommendations that are delivered into existing workflows. By embedding intelligence throughout the entire omnichannel ecosystem, Aktana makes every customer journey feel like a continuous conversation--seamless, well-timed and always relevant. Today, more than half the top-20 pharmaceutical companies worldwide use Aktana’s AI-enabled Contextual intelligence Engine to coordinate and optimize personalized omnichannel interaction at scale.

Scitara DLX™ provides a fast connectivity infrastructure for any instrument used in life science laboratories. It is fully compliant and auditable, and can be accessed from any cloud-based platform. Scitara™, a universal digital data network, connects all instruments, resources, apps, and software within the laboratory. The cloud-based platform, which is fully auditable, connects all data sources in the lab, allowing data to flow freely across multiple endpoints. Scientists can now spend their time on scientific research and not waste it trying to solve data problems. DLX corrects and curates flight data to support the creation of precise, structured data models that feed AI/ML systems. This supports a successful digital transformation strategy for the pharma and biopharma sectors. The ability to access scientific data allows for faster decision-making and drug discovery, which helps bring drugs to market quicker.

Axtria DataMAx™, the next-generation global cloud-based commercial Life Sciences Data Management product, enables accelerated business insights from trusted data. Axtria DataMAx™ facilitates rapid integration of all major structured as well as unstructured data sources in life sciences. It is secure, accurate, and compliant with the industry. To ensure that data is safe and reliable, business management rules and data quality are applied. Users can create data marts for downstream consumption and reporting by models, analytics systems, or individual data stewards.

The Life Sciences industry has been subject to nearly $15 billion in compliance-related settlements and fines over the past few years. It is therefore critical that companies adhere to best practices in pharmaceutical, biotech, and medical device manufacturing. A well-managed clinical trial can have a significant impact on the development time, budget, and scope of a drug or medical device. OpenText™, Clinical Trial Quality Management System, (ctQMS) allows companies to remain compliant, reduce the cost of records management, and establish best practices through collaboration during, and after, the clinical trial.

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.

Revolutionizing life sciences procurement. AI-powered digital market for complete transparency in your supply chain. Labviva integrates into your existing purchasing software, providing you with actionable insights that will help you make better decisions. You can keep your current suppliers, your contract pricing, your purchasing software, and your processes. Our digital marketplace provides unparalleled visibility into your purchasing process to enable informed decisions and drive science forward, without interruptions to research. Labviva integrates seamlessly with your existing procurement software, and provides actionable insights on everything from lab purchasing trends to the health of your supply chain. You can be up-and-running in just a few weeks, without having to install any software. Labviva integrates with your internal eProcurement System and unifies purchasing requirements and the requirement for scientific or technological information. You can maintain your preferred vendor's contract pricing.

Genedata Biologics®, streamlines the discovery of biotherapeutics. This includes bispecifics and ADCs as well as TCRs, CARs-Ts, CARs-Ts, CARs, and AAVs. It integrates all discovery workflows, making it the most popular platform in the industry. This allows you to focus on innovation and is the most widely used. A first-in-class platform that digitalizes biotherapeutic discovery accelerates research. The platform simplifies complex R&D processes by allowing for the creation, tracking, testing, and evaluation of novel biotherapeutics drugs. It can work with any format: antibodies, bi- and multi-specifics as well as ADCs, novel scaffolds, therapeutic proteins, and engineered therapeutic cell line such CAR-T cells and TCRs. Genedata Biologics acts as a central data backbone that integrates all R&D processes. This includes library design, immunizations, selections, panning, molecular Biology, screening, protein engineering and expression, as well as candidate development and manufacturability assessment.

Our cutting-edge platform, the Medidata Clinical Cloud, transforms clinical trial experiences for patients, sponsors and CROs. The Medidata Clinical Cloud is the only unified technology platform that focuses exclusively on clinical research. It addresses every step of the research process, from start to finish. Our platform helps medical device and life science organizations reduce development costs, minimize risks, and bring treatments and devices to market quicker. The Medidata Clinical Cloud will allow you to access the power of any product you choose for your clinical trials program. Medidata is leading the digital transformation in clinical research. Our platform, powered by artificial intelligence, machine-learning, advanced analytics, and advanced research, brings together researchers, study managers and investigators to accelerate research. Obtain regulatory-compliant, patient-friendly electronic informed consent for clinical trials.

Tovana is a science driven methodical approach to connecting data Science with deep pharma domain expertise. It uses advanced Machine Learning (ML technology) to solve the challenges of creating and executing a winning HCP Engagement strategy in a continuous, optimal way. You will see a significant increase in growth by streamlining your Go to Market strategy. This is achieved by combining human knowledge with AI/ML technology to close the gap between strategy execution and strategy. Tovana encourages self-reliance by removing the dependency upon third parties to manage strategy execution. This allows you to quickly calibrate and correct your course. Tovana gives you complete control over your business without the need to rely on third parties to generate, scrutinize and adjust strategic processes like targeting and segmentation and sales forecasting.

Protect your business, meet country-specific requirements regarding drug serialization and other rapidly-changing regulations, while processing large volumes of data with intelligence. The SAP Advanced Track and Trace application for Pharmaceuticals allows you to comply with international and regional legislation. It provides a corporate serialization repository, serial numbers management, and reporting capabilities. Reduce compliance costs for current and future serialization requirements, including country-specific reporting. Increase efficiency in your supply chain by gaining greater visibility into material movements down to the sales-unit item level. Manage large quantities of serialization data and adapt to changes in legislation. Track and trace serial numbers of retail products in a corporate repository. Report serial numbers in accordance with country-specific regulations.

Qlucore Omics Explorer makes it so simple to use that you don't have to rely on a specialist in bioinformatics for analysis and exploration of your Omics or NGS data sets. Qlucore Omics Explorer, a next-generation D.I.Y bioinformatics software, is available for research in academia, life science, and plant-tech industries. The flexible and powerful visualization-based data analysis tool delivers instant results and allows for the exploration and visualization of large data. The software was designed to allow you to choose the best workflow for your experiments and maximize the results of your research. You will be able see your results instantly by combining instant visualization with powerful statistics, flexible selection methods, and powerful statistics. You decide the workflow and starting point for your own exploration. You have complete control over the exploration process and can tailor it to your needs.

The L7 Enterprise Science Platform (L7|ESP®) is a comprehensive platform designed to contextualize data and remove business silos through process orchestration. This all-in-one solution supports the digitalization of data and scientific processes within life sciences organizations. It includes native applications like L7 LIMS, L7 Notebooks, L7 MES, and L7 Scheduling. L7|ESP seamlessly integrates with third-party applications, lab instruments, and devices to consolidate all data into a unified model. Featuring a low-code/no-code workflow designer and numerous pre-built connectors, it ensures rapid implementation and full automation. Utilizing a single data model, L7|ESP enhances advanced bioinformatics, AI, and ML to provide new scientific and operational insights. L7|ESP addresses the data and lab management needs and challenges within the life sciences sector, specifically targeting: ● Research and Diagnostics ● Pharma and CDMO ● Clinical Sample Management Explore the L7 Resource Center for on-demand recordings, case studies, datasheets, and more: l7informatics dot com/resource-center

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).

Cortellis™, a suite of life science intelligence software solutions, reveals hidden insights in data. This allows you to make better informed decisions throughout the R&D process. We have taken out the tedious work of finding, integrating and analysing data so that you can concentrate on the crucial decisions required to bring your products to market quicker. Cortellis provides unique data analysis that is rich in domain knowledge, industry insight, and therapeutic expertise. This allows you to unlock hidden insights that will allow you to make data-driven decisions that drive innovation. With the most comprehensive and deepest intelligence, you can get precise and actionable answers to specific questions throughout the R&D process. Cortellis is an indispensable part your daily work flow.

Within3 is the leader in insight management for life science teams. Our insights management platform helps identify the right people, engage them and deliver answers that enable informed, agile decision-making. Our platform was created to address the life science insight gap. Companies often base decisions on outdated or incomplete data, which can lead to huge losses in time and money. Within3's insight management platform closes the gap in product development. It can be used at all stages of the product development process, including planning, recruiting, understanding, and analysis. Within3 is trusted by the world's leading pharmaceutical companies and medical device companies to identify key professionals, engage audiences in focused discussions, gain a 360-degree view on scientific and market signals.

Imagine all your regulatory information about products, registrations and submissions, correspondence, and commitments in one central place, accessible from anywhere. Ennov RIM allows life sciences companies to streamline their regulatory processes, improve data quality, quickly respond to business-critical questions, and effectively responds to health authority requests. Ennov RIM, a purpose-built application based on Ennov Process, allows for the tracking and management of therapeutic product details as well as registration information. Ennov RIM gives regulatory personnel the essential information and functionality they need to manage product portfolios globally, whether you're planning to launch a new product or handle variations to existing registrations.