Signals VitroVivo Alternatives

Xybion LIMS (formerly Labwise XD) is an all-inclusive LIMS, ELN, QMS, and DMS. Xybion LIMS drives lab workflows, 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. Xybion LIMS creates optimized workflows for the unique business needs of all regulated laboratories including research, diagnostics, quality control, stability studies, and more.

The modern, flexible, easy-to-use LIMS. QBench enables our customers to get a LIMS up and running faster. Automate your entire lab with our developer-friendly API, Inventory Management, Customer Portal, Billing, and Quality Management System modules. QBench is a cloud-based Laboratory Information Management System (LIMS) that enables labs to streamline their entire testing workflow, from sample receiving to automated results reporting. 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. View hundreds of PDF reports/COAs before publishing or emailing. Generate barcodes and create labels that you can customize for your samples. See counts and latencies for different data types in QBench. This includes metrics like turnaround time, sample counts per test, sample delay, and more!

Labguru is a secure, cloud-based Electronic Lab Notebook (ELN), LIMS and informatics platform which offers a complete solution for life science research and industry. It records and manages laboratory data and inventory, includes molecular biology tools and chemistry tools, enables automation of the lab, insight into lab data making labs run more efficiently. With Labguru, scientists can design experiments and workflows, capture structured and unstructured data, manage projects, and share their work. Customizable experiment templates, integration of protocols, SOPs, and other cutting-edge features help to increase data quality, streamline workflows and reduce costs. Labguru is available on desktops and mobile devices via the cloud. Labguru is part of Holtzbrinck Publishing Group and serves over 100,000 scientists worldwide from startups, universities, research institutes up to some of the largest pharma companies.

Secure and scalable, the Suite features a modern, intuitive interface that offers scientists complete control in configuring workflows for every technique, modality, and data type. Signals VitroVivo 3.0 (formerly Signal’s Screening) easily transforms raw data into actionable results and Signals Inventa 3.0 (formerly Signals Lead Discovery) is the next-gen analytics software that enables researchers to seamlessly publish results from disparate data sources. Experimental data capture, materials management, and collaboration workflows in a user-friendly cloud-based electronic notebook. Flexible visual and automatable instrument data processing to drive data quality and reproducibility. Unified data management for scientific results combined with rich interactive analytics. Extensibility to integrate with internal and partner systems and processes.

ActivityBase is the established industry software platform for screening data management, with feature-rich data analysis tools, built-in object/compound registration tools and the industry standard database. ActivityBase provides analysis support for a wide range of biochemical, cellular and biophysical assay formats (including Ion Channel, FLIPR, Kinetic, SPR, Mass Spectrometry assays). The system integrates into HCS imaging stores (Perkin Elmer Columbus, Thermo Fisher HCS Studio, Molecular Devices MDCStore) for easy import of data and images. ActivityBase also features built-in compound registration and plate management tools. With ActivityBase, you can easily track and manage the results from years of assays in one system. The system can be configured to meet your needs, without having to buy new analysis packs, and, through improvements in your data analysis processes, can even increase your lab analysis tenfold.

Through our diverse and growing community, Genoox accumulates the most relevant database and delivers actionable, real-world genomic insights that impact lives, improve clinical outcomes, and shape the business of healthcare. Our solutions are changing the face of genomics. Genoox uses the power of its community and combines public data with community data to streamline the path from DNA sample to clinical report, impacting patient care by making genomic data accessible and actionable at the point of care. Genoox enhances research and life sciences companies by providing an insight platform derived from real-world data and evidence and powered by our community with robust genomic analytics, helping researchers simplify complex genomic data and make impactful discoveries using the most advanced genetic tools and applications. Genoox helps biosystems companies such as DNA sequencing companies to bundle its state-of-the-art genomic engine with dedicated assays.

Novatek’s Clinical Assay Management software is a unique information management application that provides a consistent approach to the collection, management and integrity of clinical research study data. Novatek’s Clinical Assay Management software tracks and manages all sample data throughout its whole analytical process and ensures a single verifiable version for all clinical and analytical data sets. Novatek’s Clinical Assay Management software `helps organizations manage their studies based on a particular product that is being developed. In addition, this application will give clinical studies the structure that is required to ensure all related steps are executed in a timely manner.

Scilligence’s RegMol is an entity registration and bioassay database which supports all entities. Our comprehensive and easy-to-deploy platform enables centralized management of protocols and assay data to support all research and development collaborations. RegMol empowers data driven decisions through our powerful data mining analytics including query by chemical structure, HELM and biosequences. Our innovation is driven by the idea that the best solutions come from shared experiences. We’ve built a tool that makes it easy to share knowledge and resources with colleagues globally. We understand that it can be difficult to wrangle all of the data you need to make industry-changing discoveries. Our ELN is a flexible web platform that allows you to easily find and organize unstructured data. Our advanced search and indexing capabilities allow researchers to quickly search and filter through unstructured data.

With visual analytics powered by TIBCO Spotfire®, PerkinElmer Signals Translational provides all the necessary tools to harmonize, manage, search, aggregate and analyze data consistently across large datasets for use in translational research in a highly scalable manner. Powered by the industry-leading visual analytics platform TIBCO Spotfire®, Signals Translational enables precision medicine studies with the most advanced biomarker discovery and patient stratification solution available today. The Linear Mixed Effect App (LME) in Signals Translational allows scientists to rank the effect of multiple variables on a phenotype of interest, with the option to correct the effect of random variables in the analysis. The genes with the strongest impact on cancer stage progression can be identified independently of the origin of the patients. With the advantage of properly handling missing values and outliers, LME models are an effective tool to identify potential biomarkers.

Today’s biopharmaceutical industry is marked by complexity: growing market demands for improved specificity and safety, novel treatment classes and more intricate mechanisms of disease. Keeping up with this complexity requires a deeper understanding of therapeutic behavior. Modeling and simulation methods provide a unique means to explore biological and physicochemical processes down to the atomic level. This can guide physical experimentation, accelerating the discovery and development process. BIOVIA Discovery Studio brings together over 30 years of peer-reviewed research and world-class in silico techniques such as molecular mechanics, free energy calculations, biotherapeutics developability and more into a common environment. It provides researchers with a complete toolset to explore the nuances of protein chemistry and catalyze discovery of small and large molecule therapeutics from Target ID to Lead Optimization.

JADBio is a state-of-the-art automated Machine Learning Platform without the need for coding. With its breakthrough algorithms it can solve open problems in machine learning. Anybody can use it and perform a sophisticated and correct machine learning analysis even if they do not know any math, statistics, or coding. It is purpose-built for life science data and particularly molecular data. This means that it can deal with the idiosyncrasies of molecular data such as very low sample size and very high number of measured quantities that could reach to millions. Life scientists need it to understand what are the features and biomarkers that are predictive and important, what is their role, and get intuition about the molecular mechanisms involved. Knowledge discovery is often more important than a predictive model. So, JADBio focuses on feature selection and its interpretation.

Signals Inventa, formerly known as Signals Lead Discovery, is a next-generation data management system for the analysis of scientific results. Powered by PerkinElmer’s innovative Signals Data Factory technology it enables you to efficiently access and analyze all scientific results collected throughout the research and development lifecycle. No matter what you make, Signals Inventa helps you decide which tests offer the best results, what you should make next, what to test further, and lots more. With Signals Inventa, data is normalized, staged, and ready to explore. Signals Inventa expands scientific understanding with a range of scientific-analytical methods, including R-group decomposition, chemical clustering, matched molecular pair analysis, maximum chemical substructure, blast search of both internal and external databases, and sequence alignment.

The Synthace digital experiment platform lets you design powerful experiments, run them in your lab, then automatically build structured data. Synthace DOE is an adaptive design of experiments solution that makes sophisticated, multifactor experiments available to anyone–all defined, executed, and analyzed in one place. High throughput DOE automation and data isn't a pipe dream, it's already here. Unleash your equipment to work full pelt on the hardest problems you need to solve today, tomorrow, and every other day after that. Run V1 in the morning, then V2 after lunch. With Synthace's dynamic automation, you can update your experiments as often as you like, without (re)writing code: run your experiments this way, then that way, then back again. Act on your decisions with lightning speed. Automatically gather and structure your experiment designs, experimental data, and metadata, all in one platform.

NVIDIA® Parabricks® is the only GPU-accelerated suite of genomic analysis applications that delivers fast and accurate analysis of genomes and exomes for sequencing centers, clinical teams, genomics researchers, and high-throughput sequencing instrument developers. NVIDIA Parabricks provides GPU-accelerated versions of tools used every day by computational biologists and bioinformaticians—enabling significantly faster runtimes, workflow scalability, and lower compute costs. From FastQ to Variant Call Format (VCF), NVIDIA Parabricks accelerates runtimes across a series of hardware configurations with NVIDIA A100 Tensor Core GPUs. Genomic researchers can experience acceleration across every step of their analysis workflows, from alignment to sorting to variant calling. When more GPUs are used, a near-linear scaling in compute time is observed compared to CPU-only systems, allowing up to 107X acceleration.

The Medidata Clinical Cloud is our cutting-edge platform that transforms the clinical trial experience for patients, sponsors, CROs, and research sites. As the only unified technology platform dedicated to clinical research, the Medidata clinical cloud addresses the holistic research process from start to finish. Our platform helps life science and medical device organizations cut development costs, mitigate risks, and deliver treatments and devices to market faster. No matter which products you choose for your clinical trial program, you will have access to the power of the Medidata Clinical Cloud. At Medidata, we’re leading the digital transformation of clinical research. Powered by artificial intelligence, machine learning and advanced analytics, our platform brings researchers, study managers, investigators, and patients together to accelerate research. Obtain regulatory-compliant, patient-friendly electronic informed consent for clinical trials.

Azenta Life Sciences offers scalable, powerful, and flexible informatics sample processing solutions that enable lab systems to efficiently deploy across all sites and utilize built-in project and diagnostic operations management functionality. We provide unrivaled sample exploration and management solutions to help you accelerate discovery, development, and delivery. Azenta Life Sciences offers cloud-based informatics solutions for sample processing that automate laboratory workflows and optimize staff workload through standardized processes. The software offers modules that manage clinical trials, families and patients, informed consent, storage, diagnostics, next-generation sequencing, and sample processing. Interfaces with external data sources and offers flexible options to integrate 3rd party systems and instruments.

As the leader in insights management for life science teams, Within3’s insights management platform identifies the right people, actively engages them, and delivers answers that drive informed agile decision-making. We built our platform to close the life science insight gap—a problem that leads companies to base decisions on old or incomplete data, wasting billions of dollars and years of work. The Within3 insight management platform solves the insight gap at every stage of the product development lifecycle, from planning and recruiting, to engaging, understanding, and analyzing. The world’s top pharmaceutical companies and leading medical device organizations trust Within3 to identify key experts, engage audiences in focused discussions, and obtain a 360-degree view of scientific and market signals.

OpenText™ Information Management solutions help life sciences organizations leverage insights from data and content to improve decision-making processes and accelerate product development. Integrate, manage, and securely exchange data across people, systems and things. Leverage information assets from R&D to commercialization. Freedom of choice with cloud-native software that can run anywhere. OpenText for life sciences accelerates the discovery process by extracting actionable insights that drive pipeline innovation. Capture and manage research papers into electronic lab notebooks with intelligent capture. Find insights with text mining. Extract knowledge trapped in the unstructured text contained in clinical trial reports, study protocols, clinical safety and efficiency findings. Find out how to intelligently analyze, classify and extract clinical trial documents to reduce the risk of costly stops and starts.

Scitara DLX™ offers a rapid connectivity infrastructure for any instrument in the life science laboratory in a fully compliant and auditable cloud-based platform. Scitara DLX™ is a universal digital data infrastructure that connects any instrument, resource, app and software in the laboratory. The cloud-based, fully auditable platform connects all data sources across the lab, allowing the free flow of data across multiple end points. This allows scientists to devote their time to scientific research, not waste it solving data issues. DLX curates and corrects data in flight to support the development of accurate, properly structured data models that feed AI and ML systems. This supports a successful digital transformation strategy in the pharma and biopharma industries. Unlocking insights from scientific data enables faster decision-making in drug discovery and development, helping bring drugs to market more quickly.

Actionable insights, driven by the industry's #1 AI-powered clinical analytics platform, enable your teams to manage risk and improve performance across studies, systems, sites, and vendors. State-of-the-art clintech from Saama is designed to streamline your workflows, automate time-consuming processes, and improve collaboration across clinical operations, medical review, data management, biostatistics, and pharmacovigilance. Sponsors and CROs rely on Saama for data aggregation and artificial intelligence solutions that lead to better decision-making, eliminate delays, and significantly shrink drug development costs and timelines. Saama can put you on the fast track to clinical trial process innovation. When all your clinical data is in one place and updated in real time, life’s much easier for your ClinOps and medical review teams. Data Managers have been underappreciated for too long. Eliminate manual work so they can pay attention to the data points that matter.

Meet IDBS Polar, the world’s first BioPharma Lifecycle Management (BPLM) platform, eliminating repetitive manual tasks, allowing you to efficiently execute your processes while curating the data you need to accelerate time to market by tackling the biggest challenges in process design, optimization, scale-up, and technology transfer. Interactive data analytics applications, such as bioreactor comparison designed specifically for biopharma development scientists. IDBS Polar is a platform that securely manages drug progression in contexts of workflow, integration, and insight. Workflows designed to simplify the BioPharma Lifecycle with process-aware planning, design, and execution of end-to-end bioprocess and analytical unit operations. Integrations that bring meaning to your data. Rapid integration into your development ecosystem, enabling automation and curating a process-centric data backbone.

At Genospace, we understand that genomics is driving the development of precision medicine, yet scaling its delivery is an unsolved challenge. We’re here to help. Our platform is designed to make biomedical data meaningful and accessible to everyone, especially those on the front lines of care delivery. Arm your clinicians and researchers with the information they need to make informed decisions and join us in our mission of leveraging high-dimensional molecular data to improve individual patient outcomes and accelerate drug development and research. Large-scale population data is necessary for drug development and research. Conduct cohort-driven analyses to inform your research activities with the Genospace platform. We specialize in clinical trial research. Use the Genospace platform to match fragmented patient data to complex trial criteria and expedite patient accruals. Integrate genomic medicine into mainstream clinical care with the Genospace platform.

End-to-end regulatory information management on a single platform. The Vault RIM Suite streamlines global regulatory processes on a single, cloud-based platform, enabling life sciences companies to improve visibility, data quality, and agility. Respond faster to changing regulations and increase process efficiency from submission planning to publishing. Coordinate regulatory efforts across HQ, affiliates, and partners within a single RIM system. Ensure teams are developing reliable regulatory content with high data integrity. Veeva Vault Registrations manages product registration data worldwide, including registration status, variations, and health authority interactions. Veeva’s flexible data model accommodates IDMP data points and will continue to support evolving regulatory data standards. Veeva Vault Submissions streamlines submission planning through approval by automating regulatory process steps.

Genedata Biologics® streamlines discovery of biotherapeutics including bispecifics, ADCs, TCRs, CAR-Ts, and AAVs. The most widely adopted platform across the industry, it integrates all discovery workflows so you can focus on true innovation. Accelerate research with a first-in-class platform uniquely designed from the start to digitalize biotherapeutic discovery. The platform facilitates complex R&D processes by designing, tracking, testing, and assessing novel biotherapeutics drugs. It works with any format, from antibodies, bi- or multi-specifics, ADCs, novel scaffolds, and therapeutic proteins, to engineered therapeutic cell lines such as TCRs and CAR-T cells. Acting as a central end-to-end data backbone, Genedata Biologics integrates all R&D processes, from library design and immunizations, selections and panning, molecular biology, screening, protein engineering, expression, purification, and protein analytics, to candidate developability and manufacturability assessments.

Extract valuable insights from an expansive number of sources in a centralized location, thereby accelerating the tedious manual review process, increasing productivity, and acquiring a deeper understanding of complex, scientific content. Leverage Intelligent Literature Monitoring to proactively collect, evaluate, and document post-market performance data to ensure In Vitro Diagnostic Medical Devices Regulations (IVDR) and Medical Devices Regulations (MDR) compliance. Leverage Intelligent Literature Monitoring to quickly and easily compare medical guidelines and update visual decision-making trees. Leverage our free, open-source content ingestion framework to extract text from a wide variety of data and document types. Sorcero’s Language Intelligence platform is empowering life science and STEM enterprises with immediate access to powerful insights to augment expertise and decision-making.

Ennov Regulatory Suite, a world-class regulatory content and information management is a unified, centralized, end-to-end solution that is robust enough to support the regulatory information workflow from the earliest stages of research and development through market authorization. It is a common principle shared by companies striving to achieve regulatory operational excellence. These companies understand that an such a solution will help them drive harmonization, promote standardization, improve collaboration, ensure compliance, eliminate waste, reduce costs, accelerate product release and allow them to operate and compete more effectively in global markets. The Ennov Regulatory suite combines the power and flexibility of Ennov Doc, Ennov Dossier and Ennov Process to support the entire regulatory product lifecycle from the early planning of registration targets through product retirement. The Ennov Regulatory suite is an invaluable tool for regulatory activity planning.

Mednet is a healthcare technology company specializing in eClinical solutions designed for the global life sciences community. Mednet’s flexible, electronic data capture (EDC)-centric eClinical platform improves the efficiency of clinical studies of all types and sizes. Beyond simply EDC, Mednet’s comprehensive solution set provides the tools required to build and manage all types of clinical research, while adapting to evolving demands and requirements. Pharmaceutical, medical device, biotechnology and Contract Research Organizations (CROs) around the world have trusted Mednet for nearly 20 years to deliver the technology innovation, experience and reliability they need for success. For more information, visit mednetsolutions.com.

Partek bioinformatics software delivers powerful statistical and visualization tools in an easy-to-use interface. Researchers of all skill levels are empowered to explore genomic data quicker and easier than ever before. We turn data into discovery®. Pre-installed workflows and pipelines in our intuitive point-and-click interface make sophisticated NGS and array analysis attainable for any scientist. Custom and public statistical algorithms work in concert to easily and precisely distill NGS data into biological insights. Genome browser, Venn diagrams, heat maps, and other interactive visualizations reveal the biology of your next-generation sequencing and array data in brilliant color. Our Ph.D. scientists are always just a phone call away and ready to help with your NGS analysis any time you have questions. Designed specifically for the compute-intensive needs of next-generation sequencing applications with flexible installation and user management options.

ChemOffice enhances scientists’ personal productivity and helps them do better science by enabling them to organize and explore their compounds, reactions and associated properties so that data can be turned into actionable information, and decisions can be made with greater confidence. ChemDraw for Excel adds chemical intelligence to Excel spreadsheets so that chemists can use Excel’s analysis, sorting and organization tools to further manipulate and enrich sets of compounds and data and explore structure-activity relationships. Chem3D generates 3D models so that chemists can view their compounds in three dimensions to assess shape and properties to maximize activity or specificity. ChemFinder is a chemically-intelligent personal database system that scientists use to organize their compounds and to search for and correlate structures with properties.

OmicsBox is a leading bioinformatics solution that offers end-to-end data analysis of genomes, transcriptomes, metagenomes, and genetic variation studies. The application is used by top private and public research institutions worldwide and allows researchers to easily process large and complex data sets, and streamline their analysis process. It is designed to be user-friendly, efficient, and with a powerful set of tools to extract biological insights from omics data. The software is structured in different modules, each with a specific set of tools and functions designed to perform different types of analysis, such as de-novo genome assemblies, genetic variation analysis, differential expression analysis, and taxonomic classifications of microbiome data, including the functional interpretation and rich visualizations of results. The functional analysis module includes the popular Blast2GO annotation methodology and makes OmicsBox particularly suited for non-model organism research

Deliver explainable imaging AI faster and more accurately with Zegami. Our full-stack service enables researchers, data scientists and medical practitioners to deliver explainable imaging AI with greater efficiency and accuracy. Our team and tools become your data science plug-in, to ​create, enhance and validate machine learning models in healthcare, life sciences and manufacturing, to drive your business or project forward.​

A platform that connects scientific rationale, compound design, and computational resources. Chemaxon’s Design Hub for medicinal chemistry from analysis to prioritize ideas. Design Compounds and manage ideas within one platform. A single platform that connects scientific rationale, compound design, and computational resources. Switch from PowerPoint files to graphical and chemically searchable hypotheses that are an integral part of the compound design process. Easily work with your trusted phys-chem properties, computational models, novelty issues, or purchasable compound catalogs in a rich visual environment. Involve your CROs in the compound progression process using this secure online service. Analyze collected evidence from biological assays or experimental structural information, extract SAR, and make new hypotheses for the next optimization iteration. Store your scientific hypotheses in a “designer's ELN” (chemically aware drawing canvases).

Accelerate scientific discovery and empower your R&D team with harmonized data in the cloud. The Tetra R&D Data Cloud combines the industry’s only cloud-native data platform built for global pharmaceutical companies, with the power of the largest and fastest growing network of Life Sciences integrations, and deep domain knowledge, to deliver a future-proof solution for harnessing the power of your most valuable asset: R&D data. Covers the full life-cycle of your R&D data, from acquisition to harmonization, engineering, and downstream analysis with native support for state-of-the-art data science tools. Vendor-agnostic with pre-built integrations to easily connect to instruments, analytics and informatics applications, ELN/LIMS, CRO/CDMOs. Data acquisition, management, harmonization, integration/engineering and data science enablement in one single platform.

Legacy R&D software is a drain on scientific potential. It slows down R&D progress, scatters data across silos, and wipes out institutional knowledge. Benchling is the industry’s leading life sciences R&D cloud. Accelerate, measure, and forecast R&D – from discovery through bioprocessing – all in one place. A suite of seven natively unified applications that accelerate R&D at all levels. Codeless configuration, open integration, and dashboards tailored to your needs. Deep life science R&D and consulting expertise ensure ongoing success. Benchling is a unified R&D platform, so you spend less time entering and hunting for data, and more time working together to move your research forward. Scientists, managers, and executives can optimize R&D output with complete visibility into experimental context, program performance, and resource utilization.

Providing a secure, cloud-based platform, longitudinal EHR data, and analytic tools to help providers and life sciences companies find new connections among previously siloed healthcare data. A set of SaaS applications designed to enable rapid population management, performance measurement, and effective engagement to patients and providers. Enables healthcare systems to collect, link, and combine data from hundreds of disparate sources across their enterprise and clinically integrated networks. Enables care and quality program designers to search and browse populations surrounding diagnoses, treatment, outcomes, costs and demographics. Quickly identifies target populations to help you make better decisions about risk-stratified care management. An integrated framework for correlating billions of clinical, operational and financial events into benchmarks and scorecards for comparison.

Single-Source-of-Truth commercial data management service with fully integrated customer master data management and business intelligence. Pharma companies don’t have to choose between the high price and long timelines of a consulting engagement or the heavy overhead and operational limitations of SaaS solutions. Mosaic clients get the high touch service and customization of a consulting engagement with the more predictable cost of a SaaS solution.

PharmaWorx helps to close the loop between marketing activities and customer feedback by offering real-time data capture and customer responsiveness, thus enhancing the overall relationship with the customer. Med Reps that use PharmaWorx can make a planned or informal visit to a doctor's office, instantly switch on their iPad or Android tablet and present product information to the doctor along with completing previously recorded tasks or capturing notes for the current visit, as well as drop off samples. If a doctor is interested in a particular image, video or brochure, the med rep can mail the content directly from the iPad to the doctor's email while still at the doctor's office.The solution is flexible and can be easily integrated into any Enterprise Resource Planning or Supply Chain Management solution for immediate and up-to-date access to business information.

L7 Enterprise Science Platform (L7|ESP®) is a unified platform that contextualizes data and eliminates business silos via process orchestration. It's a comprehensive solution that facilitates the digitalization of data and scientific processes in life sciences organizations. L7|ESP has native applications, including L7 LIMS, L7 Notebooks, L7 MES, L7 Scheduling, and more. It can integrate with existing third-party applications, lab instruments, and devices to capture all data in a single data model. It has a low-code/no-code workflow designer and hundreds of pre-built connectors to enable rapid time-to-value and end-to-end automation. By leveraging a single data model, L7|ESP enables advanced bioinformatics, AI, and ML to offer novel scientific and operational insights. L7|ESP addresses data and lab management needs in life sciences, particularly in: ● Research and Diagnostics ● Pharma and CDMO ● Clinical Sample Management Resource Center: l7informatics dot com/resource-center

Unite and free your unstructured health data Interactive AI and NLP solution delivering health insights to Providers. Payers. Life Sciences. Interactive AI and NLP solution to unlock health insights from unstructured clinical notes data for: Provider. Accelerate data abstraction from and clinical validation of information contained in clinical notes. Decrease time and reduce costs required to identify care gaps, review care quality dashboards, and generate registry reports. Payer. Integrate and analyze both claims data and clinical notes to more effectively manage high risk and high cost member cohorts. Life Sciences. Rapidly match patients to clinical trials–and vice versa–using clinical trial databases and data from clinical notes. Leverage the power of real world clinical data and evidence. Ember is an end-to-end solution at the intersection of NLP and predictive analytics. Streamline. Healthcare Analytics for Unstructured Data to Improve Quality, Efficiency, and Outcomes

Aetion Evidence Platform® delivers real-world evidence for life sciences companies, payers, and at-risk providers. We help you answer the high-stakes questions in health care: what works best, for whom, and when. Because better answers lead to better decisions. As a partner to the majority of the top 20 global biopharma firms, leading payers, and the FDA, Aetion informs the most critical decisions in the industry. Our transparent analyses guide product development, commercialization, and payment innovation into health care’s modern era. Aetion Evidence Platform moves the application of real-world evidence from descriptive analytics to causal conclusions. And it delivers answers within days and weeks—the rapid results needed to improve clinical and financial outcomes. Turn your best available information into insights you can use now.

Rumi is a secure, compliant virtual engagement platform designed to host interactive digital discussions between your KOLs or other stakeholders. Developed specifically to meet the needs of life sciences and healthcare organizations engaging with medical professionals, patients and carers, Rumi is a stakeholder collaboration solution that makes it simple to host a virtual advisory board, patient panel, or KOL community wherever your participants are based. Accessible via desktop or device, Rumi offers several virtual engagement applications that each provide high convenience for stakeholders, at a low cost for sponsors. The platform enables deeper engagement and insights for more actionable results than video conference or face-to-face methods, and the ability to target the outcomes you need. Who is Rumi for? Rumi is for any healthcare brand, organization, agency or consultant who’s seeking deep and considered insights from their stakeholders.

Cognidox is an online document management system for high-tech, medical device and life sciences product development sectors. Available in the cloud or as an on-premise solution, Cognidox promotes better product lifecycle management and knowledge transfer from developers to clients, partners, and customers. Secure and reliable, Cognidox provides plug-ins for various programs such as Microsoft Office, and we also offer a robust API so that you can integrate almost any process with Cognidox In addition to the core function as a DMS, an add-on for Cognidox also offers a way of allowing licensing and distribution of documents to third parties via fully sandboxed site so you have the power to publish specific documents whilst keeping your main storage secure. Another popular add-on is the gBMS - graphical Business Management System, Use Visio to easily capture your business processes, a good BMS should give you clear oversight of your entire operation.

End-to-end Product and Process Data Management. Skyland PIMS® provides emerging & global drug sponsors and CMOs a collaborative workspace to manage critical development, manufacturing and quality data. Our cloud-based, validatable software allows for fast deployment and low TCO. Maintain data content, understanding, and control across the supply chain. Faster and more efficient scale-ups, tech transfers, and commercial releases. Capture batch data and access summary dashboards for data monitoring, release status, analysis and reporting. Manage product and process specifications and target control limits. Easily create an audit trail. Automatically integrate Batch and Limits data to produce process analysis and control charts. Fulfill CPV/APR reporting requirements. Persistent product and process data library for data transparency and integrity across global networks. Streamline product and process data management throughout the product lifecycle and supply chain.

With decades of industry experience, our platform is the only one designed specifically for the unique needs of life science companies. R&D Logic allows your team to explore plans and actuals from many perspectives, so you always know exactly how your business is performing. R&D Logic’s high-touch approach means we take care of you, from implementation to training, to ongoing support, and even to expert consulting. We manage and maintain the backend to keep your data secure and private, so you can focus on managing your business. We strive to understand your unique needs and configure the right combination of products and logic that support your business. R&D Logic’s platform evolves along with you as you grow. Add, remove and modify features and business rules as your needs change. We always put our customers first, whether they’re small, medium or large, pre-commercial or commercial, or pharmaceutical, biotech or medical device businesses.

Developed specifically for the life sciences industry, eCADinfo is a 21 CFR Part 11 compliant engineering data management system designed to reduce costs and improve efficiency, productivity and compliance in FDA-regulated environments. eCADinfo stores engineering data in a wide variety of formats that include engineering drawings, equipment/system specification databases, web links to supplier sites, spreadsheets containing device parameter data, procedures, manuals, and shop sketches. The system allows you to organize this data in a structured hierarchy of meaningful information that best meets your existing business processes. The rich graphical user interface provides a wealth of information at a glance for ease of system maintenance and control. Engineering data management features include version control, collaboration, change management, standardization and a 21 CFR 11 compliant Excel spreadsheet environment.

Give your business easy access to clean, unified data from a variety of sources without a single line of code. Lore IO's AI and prebuilt ecosystem of source connectors allow fast onboarding of any source. The business friendly UI allows easy customization to changing business needs. Unified data plays a key role in the development of your product, from clinical trials to a successful product launch. So why rely on expensive, inflexible, prebuilt solutions that do not scale with your needs? And why go with custom-built solutions that are complex and require significant resources to scale with you? The Lore IO Life Sciences Cloud Analytics solution provides a simple, build-as-you-grow approach to ensuring data is accessible for business teams every step of the way. Our pre-packaged solution easily integrates with your data sources* and starts providing insights in weeks, not months.

Infor PLM for Process (Optiva®) is specifically designed for food, beverage, chemicals, and life science manufacturers and provides a unified product view of data and processes across organizations. It helps manufacturers easily achieve regulatory and labeling compliance, whether it’s meeting reporting requirements, complying with labeling laws, or supplying ingredient details. Project management capabilities give the right people the right visibility into project data, from concept, to development, to final sign-off. Reckitt Benckiser (RB), a British multinational consumer goods company, adopts modern PLM capabilities using Infor® PLM for Process to boost global safety and compliance and get one version of the truth about its products, from development to manufacturing. Integration capabilities with ERP systems helps provide better insight into costs.

Make it easy for healthcare organizations, including hospitals and clinics, health plans and life sciences, to connect with app developers and health data partners to build new FHIR API-based digital services. Improve the efficiency and safety of transitions across the continuum of in-patient and out-patient care. Provide targeted personal wellness and prevention guidance to at-risk participants. Empower collaboration between patients, physicians, and healthcare providers to effectively manage chronic conditions. Improve chronic condition management. Deliver patient-centric digital services. Reduce risks during care transitions. Manage, secure, and scale APIs with an enterprise-grade platform that is FHIR-server agnostic. Easily ingest healthcare data from internal, external, or open-source FHIR-ready partners. Deliver on the promise of patient-centric healthcare and data interoperability by quickly launching digital services like new mobile apps.

Qlucore Omics Explorer is so easy to use that you no longer have to depend on an expert in bioinformatics to explore and analyze your Omics and NGS data sets. Qlucore Omics Explorer is a D.I.Y next-generation bioinformatics software for research in life science, plant- and biotech industries, as well as academia. The powerful and flexible visualization-based data analysis tool with inbuilt powerful statistics delivers immediate results and provides instant exploration and visualization of big data. The software is developed to allow the workflow which best suits you and your experiments and maximizes the outcome of your research. By combining instant visualization with powerful statistics and flexible selection methods, you will be able to see your results immediately. As a user, you decide your own workflow and starting point. You are in control and can tailor the exploration to meet your specific needs.

Logilab® ELN is Agaram’s time-tested Electronic Lab Notebook (ELN) solution designed to make laboratories completely paperless by enabling them to record, execute & store their tests, experiments, and lab tasks in a secure secure central database. Logilab® ELN is used by laboratories conducting tests & experiments across various scientific fields, and by researchers/organizations involved in project & product development in regulated and non-regulated industries. It ensures that laboratory organizations can aim to achieve higher productivity, better quality and compliance to various statutory compliance standards as well as Good Lab Practices (GxP) principles of data integrity. It helps labs with the following: • Simple interface to design lab templates for tasks & experiments. • Dynamic Inventory Management • User-configured dynamic reports & document creation. • Automate instrument data capture