Alternatives to Reliant AI

IDBS Polar is the first BioPharma lifecycle management (BPLM) platform in the world. It eliminates repetitive manual tasks and allows you to execute your processes efficiently while curating data. This will allow you to accelerate the time to market, by tackling the most challenging challenges of process design, optimization scale-up and technology transfer. Interactive data analytics applications such as bioreactor comparision designed specifically for biopharmaceutical development scientists. IDBS Polar is an integrated platform that manages drug progress in contexts such as workflow, integration and insight. Workflows designed for the BioPharma lifecycle, with process-aware design, planning, and execution. Integrations that give meaning to your data. Rapid integration into your development environment, enabling automation, and curating a data backbone based on processes.

Pluto was founded in 2021 by the Wyss Institute of Harvard University. It has been a trusted partner for many life sciences organizations across the country, from biotech start-ups and public biopharma companies. Our cloud-based platform allows scientists to manage all their data, run bioinformatics analysis, and create interactive visualizations that are published-quality. The platform is being used for a variety of biological applications. These include preclinical and translational science research, cell and gene therapies and drug discovery and development.

Stop messing around with broken informatics tools and cloud infrastructure. Get started today on uncovering biological insights. Scientists are often limited by the fragmentation of tools across biology and bioinformatics teams. To help teams accelerate their R&D, we created a harmonized platform for bioinformatics between the cloud and the wet lab. Import raw data from your cloud service provider, your team's instruments, or your cloud. Create and deploy custom bioinformatics workflows using any language. Stop wasting time tinkering with your infrastructure. You can easily run any workflow and keep track of every analysis. Interactive visualizations of NGS data ready-to-go with point-and click plots Latch integrates with your AWS S3. You can access hundreds of terabytes in organic filesystems you are familiar with. Create bioinformatics workflows, and dynamically create no-code interfaces with Python with tunable storage and compute.

StarDrop™, a comprehensive suite of integrated software, delivers the best in silico technology within a highly visual interface. StarDrop™, which allows seamless flow between the latest data, predictive modeling, and decision-making regarding the next round or synthesis, improves the speed, efficiency and productivity of the discovery process. A balance of different properties is essential for successful compounds. StarDrop™, which guides you through the multi-parameter optimization challenge, helps you target compounds with the highest chance of success. It also saves you time and resources by allowing you to synthesize fewer compounds and test them less often.

We build products with our in-house chemists, biologists and clients to deliver outstanding performance and scientific understanding. Chemaxon offers a wide range of products, including out-of-the box solutions for scientists and IT professionals. It also includes components that add extra functionality as well as integrations with 3rd-party software, such Microsoft Excel or KNIME. Chemaxon, a leading software provider, is trusted by more than one million users. Its industry-leading tools for scientific discovery include calculation, search, and drawing tools. Our applications are used widely in education and research in the life sciences. Our clients come from a wide range of industries. The majority of major pharmaceutical companies are among them. Our offices are located at Budapest, Basel and Boston, with distributors all over the world.

Our global data-sharing networks generate clinically actionable insights to improve patient outcomes globally. SOPHiA GENETICS is on a mission to build the future in AI-assisted medical care. We are integrating multimodal data from healthcare-omics, unlocking existing data silos and developing machine learning models in order to produce actionable insight that can eventually support healthcare professionals improve patient outcomes. The new interface, features, and cutting edge capabilities will accelerate precision medicine workflows and bring us closer to democratizing the data-driven medicine.

The XetaBase platform is unique in that it simplifies tertiary analyses by aggregating, indexing and enriching secondary genome data. This allows for a continual reinterpretation of the data to unlock clinical and research insights. XetaBase enables the rapid management of genomic data and its cost-effective use in the laboratory and clinic. XetaBase is a genomic-scale platform. The greater the volume and the complexity, the better the insights and outcomes. XetaBase, a genomic-native platform, is built on the OpenCB open-source software platform. It meets the demands of genomic medicine for speed, scale, and reinterpretation. Zetta Genomics provides genomic data management that is fit for the precision-medicine age. XetaBase offers a novel solution for the challenges of genomic information. It replaces outdated flat file approaches and brings meaningful and actionable genome data to the lab and clinic. XetaBase allows for continual reinterpretation and scales seamlessly as databases expand to include genome sequences.

Metabolon offers the largest Level 1 library available in the metabolomics field. Over 5,400 entries are contained in our proprietary library, which has been built over 20 years. The majority of entries are Level 1, accounting for approximately 85% of our library (4,600 entries). However, some are level 2 (approximately 15 % of the entries), due to a lack commercial standards to qualify for Level 1. Metabolon's unmatched library breadth, industry-leading annotation confidence level and unmatched library depth enable us to provide our clients with accurate, highly actionable insight for their scientific or clinical inquiries. Metabolomics is applicable to a wide variety of research, including soil health, food nutrition, preclinical research and clinical trials. Whether you are looking for trends within a group, or modifying an individual's treatment plan, metabolomics will help you find the answers you need.

Geneious Prime makes bioinformatics more accessible by transforming raw information into visualizations which make sequence analysis intuitive. Simple assembly of sequences and easy editing contigs. Automatic annotation of gene prediction, motifs and translation. Genotype microsatellite trace with automated ladder fitting, peak calling, and generation of tables of alleles. A highly customizable sequence view displays beautiful visualizations of annotated assemblies and genomes. SNP variants analysis with powerful SNPs, RNA-Seq analysis and amplicon metagenomics. Create your own searchable database of primers for PCR and sequencing and design and test them. Geneious Biologics offers a flexible, scalable and secure way to streamline antibody analysis workflows. It allows you to create high-quality libraries, and select the best therapeutic candidates.

Polly allows you to harness the power of biomedical information. The Polly Platform allows you to scale batch jobs, workflows and visualization applications. Polly supports resource pooling, optimizes resource allocation based upon your usage requirements, and makes use of spot instances when possible. This results in optimization, efficiency, quicker response time, and lower costs for resources. Access a dashboard that allows you to monitor and track resource usage and costs in real-time. This will allow you to reduce overheads when resource management is done by your IT team. Polly's infrastructure is built around version control. Polly uses a combination dockers and interactive notebooks to ensure version control for your analyses and workflows. We have created a mechanism that allows data, code, and the environment to co-exist. This, along with cloud data storage and the ability for users to share projects, ensures reproducibility in every analysis.

Partek bioinformatics software provides powerful visualization and statistical tools in an intuitive interface. Researchers of all levels can explore genomic data faster and more efficiently than ever before. We turn data into discovery®. Our intuitive interface makes it easy for scientists to perform sophisticated array and NGS analysis using pre-installed workflows. Public and custom statistical algorithms can be used together to quickly and accurately distill NGS data into biological insights. Genome browser, Venn diagrams and heat maps, as well as other interactive visualizations, show the biology of your next generation sequencing and array data in vivid color. Our Ph.D. scientists can be reached at any time to assist with your NGS analysis. This product is specifically designed for next-generation sequencing applications that require high-level computing. It offers flexible installation and management options.

The Bioconductor Project aims to develop open source software that allows for repeatable and precise analysis of biological data. We encourage a collaborative and inclusive community of data scientists and developers. Resources to maximize Bioconductor's potential. Our tutorials, guides, documentation, and guides cover everything from basic functionality to advanced features. Bioconductor is an open-source and open-development software that uses the R statistical language. It has an active user base and two releases per year. Bioconductor offers Docker images with every release, and supports Bioconductor in AnVIL. Bioconductor, founded in 2001, is an open-source project widely used in bioinformatics. Over 1,000 developers have contributed over 2,000 R packages, which are downloaded over 40 million times per year. Bioconductor is cited in over 60,000 scientific publications.

Store, archive, and manage multi-omic data sets. Illumina Connected Analytics provides a secure platform for genomic data to operationalize informatics, and drive scientific insight. CWL and Nextflow allow you to easily import, build and edit workflows. Leverage DRAGEN bioinformatics pipelines. Organize your data in a safe workspace and share it with the world in a compliant way. Our platform allows you to keep your data in the cloud. Visualize and interpret data using a flexible analysis tool, such as JupyterLab Notebooks. Data warehouses allow you to aggregate, query and analyze sample data and population data. Scale analysis operations through the creation, validation, automation, and deployment of informatics pipelines. Reduce the time needed to analyze genomic data when quick results are a key factor. Enable comprehensive profiling for the identification of novel drug targets and biomarkers of drug response. Data can be transferred seamlessly from Illumina sequencing platforms.

Altis Labs launches Nota, a clinical information platform that accelerates R&D for therapeutics. AI predicts patient outcomes based on imaging data, so sponsors can prioritize their most promising treatments. Nota allows researchers to access imaging biomarkers and speed up R&D by operationalizing clinical trial imaging data. Altis' cloud software platform powered with deep learning allows biopharma to incorporate comprehensive outcomes predictions at the image level, patient level, and cohort-level in order to improve clinical trial designs and better anticipate clinical endpoints. These insights can accelerate drug development timelines and lower costs, while increasing the likelihood of success in clinical trials across therapeutic areas.

Combinatorial barcoding technology removes the limitations and frustrations associated with yesterday's single cell approach. It eliminates the need for a specialized instrument and allows you to make new discoveries. Unleash the power of a single cellular. In a single experiment you can profile up to 1,000,000 cells or nuclei, allowing for unprecedented scientific progress. Evercode's combinatorial barcoding technology is superior to droplet-based approaches. You can now expand the size of your experiment without the restrictions of the past. Get better data quality. All without the need to use finicky hardware which is already outdated. You can perform single-cell experiments using a pipette, common laboratory equipment and a pipette. Split-pool combinatorial barscoding allows for scalable single cells, without the need for a custom instrument. Scalable single-cell sequence without the instrument. Each kit includes end-to-end reagents for solution and intuitive analysis software.

Correlation Engine, an interactive omics database, places private omics data into a biological context by combining it with highly curated publicly available data. Correlation Engine, one of the largest databases in the world for life science research, provides researchers with unprecedented access and insight to a vast number of high-quality whole genome analyses. The knowledgebase allows for novel discoveries through the interrogation of billions of datapoints derived from standard analyses of whole genome studies. A suite of applications for determining biological context, a constantly growing library of curated datasets, and support of multiple species and multi-omic data sets. Use a simple graphical interface to leverage guided workflows and APIs. Accelerate the journey from omic to decision-making and gain access to more than 25,000 multi-omics studies that have been reanalyzed (from over 250.000 signatures).

Eidogen-Sertanty’s Target Informatics platform (TIP), is the first global structural informatics system. It enables researchers to examine the druggable genome from an structural perspective. TIP increases the rapidly expanding body experimental protein structure information and transforms structure based drug discovery from an inefficient, data-scarce discipline to a high-throughput science with rich data. TIP is a tool that bridges the knowledge gap between bioinformatics (bioinformatics) and cheminformatics. It provides drug discovery researchers with a knowledge bank of information that is both unique and highly complementary to existing bio- and cheminformatics platform information. TIP's seamless integration between structural data management technology and unique target-to-lead analysis capabilities enhances every stage of the discovery pipeline.

AI-powered drug discovery is a proven technology. Cerella extracts hidden insights from your drug discovery data to reveal the best compounds and most valuable experiment for your project. It can make confident predictions by accurately filling in the missing values. This is especially useful for expensive downstream experiments, which are impossible to predict using other methods. This allows you to do more with sparse and limited data sets.

The life sciences industry is among the most complex industries in the world. These companies require a flexible IT infrastructure that can control compliance costs. It is crucial to improve business performance while you strive to bring new products into the market in a timely fashion. The demand for a flexible operating environment is increasing due to the explosion of research, development and regulatory compliance. Access to real-time data on production processes and operations is critical. These data are essential for life science companies to make informed decisions, stay compliant, and run efficiently. The pressures of time-to-market, profitability and efficiency are high. Being the first company in the world to patent and market a new product can be a major indicator of success. These needs are often weighed against the demand for existing products.

A robust platform for automatic variant prioritization and clinical interpretation, as well as report generation, is essential to ensure efficient reporting of NGS-based clinical trials. Strand Omics, a cloud-based platform that is HIPAA-compliant and fast, drives our clinical diagnostics practice. It has been refined over 4 years with over 10,000 clinical reports and multiple peer reviewed publications. Strand Omics is a combination of bioinformatics algorithms and curated databases, visualization interfaces, and reporting capabilities. It offers specialized workflows that can be used for rare inherited disorders and somatic tumor profiling tests. The platform has over 10,000 variants curated to oncogenicity, 100 genes that are curated for druggability across multiple types of cancer, and 500 drugs that have been curated for evidence.

Software for fast, simple, and repeatable analysis of variants in gene panels, whole genomes, and exomes. VarSeq provides an intuitive and integrated software solution for tertiary analyses. VarSeq allows you to automate workflows and analyze variations for gene panels, whole genomes, and exomes. Our software makes it easier than ever to understand genomic data. VarSeq is a powerful software that provides a powerful filtering engine and annotation engine for sifting through large variant data. You can narrow down your list of variants quickly by using a series of filters. You can save the filters you have created after you have determined the parameters that are most effective for your analysis. This allows you to easily apply the same analysis on another dataset. VarSeq is ideal for high-throughput environments because the same automated workflow can apply to each batch of samples. Real-time filtering allows you to quickly prototype and fine-tune analysis workflows.

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

The QIAGEN CLC Geneomics Workbench is a powerful tool that works for all workflows. It is easy to overcome data analysis challenges with cutting-edge technology, unique features and algorithms that are widely used by scientists in industry and academia. Bioinformatics software solutions that are user-friendly allow for comprehensive analysis and interpretation of your NGS data. This includes de novo assembly and transcriptome assembly, resequencing analysis, WES and targeted panel support, variant calling, variant calling, RNA–seq, ChIP–seq and DNA methylation analysis (bisulfite sequence analysis). You can analyze your RNA-seq (miRNA, smallRNA) and smallRNA (lncRNA), data using easy-to-use transcriptomics workflows that allow for differential expression analysis at both gene and transcript levels. QIAGEN CLC Genomics Workbench was designed to support a wide variety of NGS bioinformatics programs.

BIOiSIMTM, a revolutionary 'virtual drug engine', is the first-in-class tool that allows drug developers to narrow down the number drugs that have potential value in treating or curing specific diseases or illnesses. We offer a variety of translational-based solutions that can be customized for your clinical and pre-clinical programs. All of these solutions are based on our BIOiSIMTM platform, which is a proven and validated platform for small molecules, large molecule, and viruses. Our models are built using data from thousands upon thousands of compounds across seven species, which gives them a robustness that is rare in the industry. The platform is focused on human outcomes and has at its core a translatability tool that transforms insights across species. The BIOiSIMTM platform is available before preclinical animal trials begin, which allows for earlier insights and saves on expensive outsourced experimentation.

Genospace understands that genomics is driving precision medicine development, but scaling its delivery remains a challenge. We are here to help. Our platform makes biomedical data meaningful, accessible and easy to use for everyone, especially those at the frontlines of care delivery. Your clinicians and researchers will have the information they need in order to make informed decisions. Join us in our mission to leverage high-dimensional molecular data to improve patient outcomes and accelerate drug discovery and research. For drug development and research, large-scale population data is essential. Genospace platform allows you to conduct cohort-driven analyses that will inform your research activities. We are experts in clinical trial research. Genospace allows you to quickly accrue patients by matching fragmented patient data with complex trial criteria. The Genospace platform enables you to integrate genomic medicine into your mainstream clinical care.

Legacy R&D software can be a drain on scientific potential. It slows down R&D progress and scatters data between silos. Benchling is the industry's most trusted life sciences R&D cloud. All the tools you need to accelerate, measure, and forecast R&D, from discovery through bioprocessing, all in one place. A suite of seven applications that are natively unified and can be used to accelerate R&D at all levels. Open integration, codeless configuration, and dashboards that are tailored to your needs. For continued success, deep life science R&D and consulting expertise are essential. Benchling is a unified R&D platform that allows you to spend less time searching for data and more time working together in order to advance your research. Scientists, managers, executives, and researchers can optimize R&D output by having complete visibility into the experimental context, program performance, resource utilization, and program performance.

Galaxy is a web-based, open-source platform for data-intensive biomedical studies. Start here if you are a new Galaxy user or consult our support resources. Install Galaxy yourself by following the tutorial. You can choose from thousands of tools in the tool shed. This instance of Galaxy uses infrastructure generously provided to it by the Texas Advanced Computing Center. Additional resources are available primarily via the Jetstream2 cloud, via ACCESS and with support from National Science Foundation. Quantify, visualize and summarize mismatches from deep sequencing data. Build maximum-likelihood trees. Phylogenomic/evolutionary tree construction from multiple sequences. Using TN-93, combine matching reads to form clusters. Remove sequences that are within a certain distance of a cluster from a reference. Estimate gene essentiality scores using maximum-likelihood.

Ruffus is a Python computation pipeline library. It is open-sourced and powerful, user-friendly, and widely used for science and bioinformatics. Ruffus was designed to automate scientific and other analyses with minimal fuss and effort. It is suitable for even the most basic tasks. Even complex pipelines can be handled. This will prevent make or scons from becoming cross-eyed and recursive. No "clever magic", no pre-processing. The lightweight syntax, which does one small thing well, is unambitious. Ruffus is licensed under the permissive MIT-free software license. This license allows for free use and inclusion in proprietary software. It is a good idea to run your pipeline in a temporary directory that is not connected to your original data. Ruffus is a lightweight Python module that can be used to build computational pipelines. Ruffus requires Python 2.6 and higher, or Python 3.0 and higher.

Improve team productivity and generate greater returns on research. Interactive data visualization allows you to share private and public data with other teams. Rosalind is a multi-tenant SaaS designed for scientists. Analyze, share, interpret, plan, validate and generate new hypotheses. Code-free visualization, AI-powered interpretation, best-in-class collaboration. ROSALIND is suitable for scientists of all levels, since it does not require any programming or bioinformatics knowledge. ROSALIND's powerful downstream analysis and collaborative capabilities make it a platform for discovery and data hub that connects experiment design, quality assurance, and pathway exploration. ROSALIND manages tens or thousands of cores of computing and petabytes in storage to dynamically scale each experiment up and down to deliver results. Share results instantly with other scientists around the world with audit tracking, so everyone can concentrate on interpretation and not the processing.

OmicsBox, a leading bioinformatics tool, offers end-toend data analysis for genomes, transcriptomes and metagenomes. It also provides genetic variation studies. The application, which is used by leading private and public research institutes worldwide, allows researchers to process large and complicated data sets and streamline their analytical process. It is designed to be efficient, user-friendly and equipped with powerful tools to extract biological insight from omics data. The software is divided into modules, each of which has a set of tools and features designed to perform specific types of analyses, such as de novo genome assemblies, genetic variations analysis, differential expression analyses, taxonomic classifications, and taxonomic classes of microbiome, including the interpretation of results and rich visualizations. The functional analysis module uses the popular Blast2GO annotating methodology, making OmicsBox a great tool for non-model organisms research.

Cellenics can help you turn your single-cell sequencing data into meaningful insights. Cellenics is an open-source analytics tool developed by Harvard Medical School for single cell RNA sequencing data. Biomage hosts the community instance. It allows biologists to explore datasets of single-cells without having to write code, and helps scientists and informaticians work together more effectively. It can take you from count matrixes to publication ready figures in a matter of hours. It can also be seamlessly integrated into your workflow. It is fast, interactive and user-friendly. It's cloud-based and scalable. Cellenics, hosted by Biomage as a community instance, is free for academics with small/medium datasets (upto 500,000 cells). Over 3000 academic researchers use it to study cancer, cardiovascular health and developmental biology.

We help healthcare systems reduce their burden by providing automated analysis, diagnosis and treatment solutions to healthcare professionals and patients around the world. Congenica was founded by pioneering work done at the Wellcome Sanger Institute in the UK and the NHS. Our products combine the latest technology, automation and AI to create a platform that is uniquely differentiating. This platform can be used in any area of human disease, where genomic data is critical to unlocking actionable insight. We are a digital healthcare company that provides software and solutions to analyze and interpret genomic data at large scale. Full automation using powerful APIs and ML, to reduce the burden of specialist staff, increase case throughput, speed up decision-making and streamline reporting. Platform for accurate, certified, and secure clinical decision support with the highest level of confidence in clinical outcome.

AI-powered medical coding and auditing. Streamline manual inpatient auditing and coding processes, improve documentation quality, and free your team to focus their efforts on high-value tasks. Semantic Health drives improvements at leading hospitals. Semantic Health uses NLP and custom clinical AI algorithms, trained by our world-class AI teams on millions of records, to parse clinical and coded information. This allows our coding engines to better understand clinical context, incorporate changes in coding rules and guidelines, and suggest high quality coding and auditory opportunities with clear evidence to the clinical documentation. AI can optimize your revenue cycle and save you time by automating labor-intensive medical auditing and coding processes. Semantic Health provides hospitals and health systems with a supercharged platform for inpatient auditing that allows a 100% review of claims data prior to billing.

This free tool provides stunning visualizations of genomic data, giving you the power to see exactly what is happening at each base pair within your samples. GenomeBrowse is a desktop application that runs natively on your computer. You no longer have to compromise on speed or interface quality in order to achieve a consistent experience across platforms. It was designed with performance in mind, to provide a faster browsing experience than any genome browser currently available. GenomeBrowse has also been integrated into the powerful Golden Helix VarSeq annotation and interpretation platform. VarSeq is a powerful tool for filtering, analyzing, and annotating your data. If you enjoy the visualization experience provided by GenomeBrowse then try it out. GB can show all your alignment data. You can find context-relevant findings by looking at all your samples together.

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.

Artificial Intelligence and RNA sequencing (RNA–seq data) are both a necessity and a way to develop therapeutics that target splicing mistakes. Machine learning allows us to quickly identify new splicing mistakes and design therapeutic compounds to correct them. SpliceCore, our AI platform for RNA therapeutics research, is what we call SpliceCore. This technology platform was specifically designed for the analysis and interpretation of RNA sequencing data. It can identify, validate and test hypothetical drug targets quicker than traditional methods. Our proprietary database of over 5 million potential RNA-splicing errors is the heart of SpliceCore. It is the world's largest database of splicing mistakes and is used to test all RNA sequencing data that is submitted for analysis. Scalable cloud computing allows us to process large amounts of RNA sequencing data efficiently at a higher speed and lower cost, thereby exponentially accelerating therapeutic innovation.

ZEVAC, an AI-powered software that empowers prescribers and ASP members, can optimize hospital antimicrobial use. Antibiotic resistance is one the most pressing public health issues of our time. ZEVAC is an AI-powered Next-Gen AMS program that helps hospitals stop unnecessary or inappropriate antibiotic use. ZEVAC's unique but very scientific approach to fighting AMR growth is unorthodox. ZEVAC's highly accurate and personalized predictions of antibiotic susceptibility can help clinicians choose the best empiric antibiotic therapy. They are based on information such as patient demographics, hospital prevalence, susceptibility patterns, and historical culture. ZEVAC's AI-driven insights can help your ASP members take proactive steps to avoid inappropriate antimicrobial use. These insights are based on real-time hospital-wide clinical data analysis.

Chat with a medical AI that provides answers, cites sources, updates medical knowledge every day, and allows you to add and select knowledge bases. Pre-train the model using 2,300+ reference datasets that have been curated by medical domain specialists. These include hundreds of terminologies and data on medical research, clinical trial, patents and population health. Indexing of multiple sources for medical research and data. Updates daily on new medical results, clinical trial, and terminologies. Prepared to process millions or even billions of documents. Scale the cluster according to your needs. A medical chatbot uses conversational AI, such as natural language processing, to interact with users, and provide them with information, advice or support. They can be used in a variety of ways. Answer general medical questions regarding diseases, health conditions and treatment options.

Our Guides use a proprietary data model and a digital platform to engage members that are difficult to reach and keep them interested. Guides listen to their members and help them to motivate themselves in ways that work. Your members will have a trusted friend and a knowledgeable insider who can help them navigate any challenges they may face. Reema is an AI-powered human confidant that members can text 24 hours a day. Our data models are used to help our Guides create text messages that reach the right people at the right time and with the right communication style. Reema combines the authentic and the automated to make it both human-friendly and scalable. Reema's data engine predicts which members are at high risk by combining public data with proprietary engagement data. Our Guides use this data to strategically intervene to prevent costly care. They engage the unengaged in the right manner and over time to improve lives and outcomes.

Reduce administrative costs, improve reimbursements and maintain compliance. RapidClaims AI magic will turbocharge your RCM. Reduce admin costs, increase reimbursements and stay compliant with ease. Our customized solutions will streamline your coding process and empower or automate your coders. Code thousands of charts quickly and accurately while meeting the unique needs of clients. Our Large Language Model can interpret unstructured information, creating a longitudinal record of patients by converting notes to structured codes and disease patterns. Never make the exact same mistake twice. Create coding rules in plain English for mass use and apply them easily to your charts, separated by code type, specialty, and coders. Take action to improve your revenue cycle by gaining a deeper understanding of the code-level trends across different sites. Our platform analyzes charts in order to identify patterns of claim denial and helps you capture these.

End-to-end Product Data Management and Process Data Management. Skyland PIMS®, provides emerging and global drug sponsors and CMOs a collaborative space to manage critical development and manufacturing data. Our cloud-based, validated software is easy to deploy and has low total cost of ownership. Maintain data content, understanding, control, and transparency throughout the supply chain. Scale-ups, tech transfers, commercial releases are faster and more efficient. Access summary dashboards to view batch data, analyze and report on release status, data monitoring, and data monitoring. Manage process specifications and target control limits. Create an audit trail easily. Automated integration of Batch and Limits data allows for process analysis and control charts. Complete CPV/APR reporting requirements. For data integrity and transparency across global networks, maintain a consistent product and process data library. Streamline product data management throughout the product's lifecycle and supply chain.

Cloudbyz Safety & Pharmacovigilance Solution, a cloud-based solution, is designed to streamline drug safety and pharmacovigilance for pharmaceutical and life sciences companies. The solution automates the process of collecting data, processing it, analyzing it and reporting it in compliance with global regulations. Cloudbyz provides end-to-end management of the pharmacovigilance lifecycle, including adverse event processing, case management, regulatory reporting, signal detection, and risk management. With Cloudbyz, you can optimize your pharmacovigilance processes, accelerate case processing, and increase the accuracy of your safety data, while minimizing risk and ensuring compliance. The benefits of our solution are listed below- 1. Improved Efficiency with Automation 2. Increased data accuracy 3. Real-time visibility 4. Improved Collaboration 5. Enhanced regulatory compliance

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.

ProSellus makes it easy to find new customers. Use data points that are meaningful for you to find new customers. You can easily search for customers by name and specialization, procedure, drug, and geography. Field Sales Reps require a simple and practical sales tool. ProSellus is a different kind of CRM. Traditional Sales Enablement Tools and CRMs are complicated. They also don't help to drive revenue for healthcare sales reps who are always on the go. This mobile sales tool was created by top medical device sales professionals. It gives your sales reps unprecedented insight into all the relationships and revenue opportunities in their territory, in addition to all the essential features of a CRM. Use data that we have provided or that you already have (or both) to help your sales reps target the right physicians at the right time and create new opportunities. ).

Select the best experts who are the most qualified in the areas that you want to achieve. With Kolexia, you can optimize your recruitment strategy of KOLs* according to your objectives. This is done through an intuitive interface that allows for precise digital and scientific qualification. Kolexia's database is unique, combining information about health experts and their work. This wealth of information allows for a more in-depth analysis on their profiles, their collaborations and their impact within their field of expertise. This approach allows us to provide a comprehensive, up-to date view from opinion leaders in order to optimize medical strategy. *KOL: Key Opinion Leader

A data integration solution for modern science that is science-aware™. The data-driven future can't be built on the legacy architectures and broken data of the past. As research data volumes and types continue to grow exponentially, siloed data management and analytics become more and more unsustainable. For most organizations, however, this data is still spread across multiple systems. If the data has been brought into one place, it's usually done by a separate SDMS tool or business intelligence tool. This does not embrace the central role and highly integrated nature of truly scientific analysis. Jarvis is a science-aware™, data integration solution designed for modern science. It connects and harmonizes all of your collective scientific intelligence including instrument and application data so that you can maximize its value. Scientists can easily access this streamlined insight in a highly searchable living knowledge graph.

The data search tools are powerful and allow for quick access to the data. A calendar that is both innovative and simple to use is a great tool for medical professionals when it comes to arranging appointments. Different report generation and data analysis tools allow you to break down different sections of representatives' work. An additional time dimension allows for analysis of changes in customer characteristics and target setting for different times periods. Online. The application connects directly to the central database. Offline. The application can be used offline without restrictions and data can be synchronized when an internet connection is available. SoftDent's newest customer relationship management (CRM), solution for pharmaceutical representatives companies is PharmaCODE. This application combines the latest technologies with all the experience we have gained over nine years of developing, supporting, and maintaining Customer Profiling.

Sapio LIMS is an advanced laboratory information management system offering a unified no-code/low-code solution that streamlines laboratory workflows. Built on the Sapio Platform, which integrates LIMS, Electronic Lab Notebooks (ELN), and Scientific Data Management Systems (SDMS), it provides purpose-built solutions for scientific research and discovery, manufacturing, and clinical diagnostics. Sapio LIMS helps to optimize laboratory operations, seamlessly integrating with lab instrumentation and existing IT infrastructure. Through its robust, scalable architecture, Sapio LIMS enhances operational efficiency and ensures compliance with GxP standards such as GMP and GLP. Solutions are available for Life Sciences R&D, Clinical Diagnostics, Lab Operations and Analytics and Enterprise Data Management.

Basil uses advanced AI and machine-learning technologies to speed up access to vital insights that drive success in medical product development. Basil unlocks intelligence from multiple disconnected data sources in a powerful SaaS platform. You can then make better decisions faster, accelerating time to market, optimizing your product strategy, driving innovation and mitigating risk. Find answers and insights for your regulatory strategy with greater efficiency. Discover vital insights into in-market quality, surveillance, and trends, which are otherwise unavailable. Discover, explore, and analyse over 500k clinical trials to gain a better understanding of the existing clinical evidence.

Only SAS offers a cloud-native, open statistical computing environment with embedded analytic software, support for data standardization, and optionally integrated analytic apps. Our analytic platform for clinical research can help you modernize and bring new therapies to market quicker to improve health. Manage and analyze data in a collaborative environment, streamline processes and deliver results more efficiently to regulatory authorities. Cloud-native solution for clinical analysis, submission, and audit trails. Includes everything you need to validate, comply with regulatory requirements, manage versioning, audit trail, and support documentation. Automated workflows, support of current and future integrations and proper management of data standards and controlled terminologies. Includes a central hub for all data, automated data analysis, better management, and analytic data preparation.