Alternatives to Bluenote
Compare Bluenote alternatives for your business or organization using the curated list below. SourceForge ranks the best alternatives to Bluenote in 2026. Compare features, ratings, user reviews, pricing, and more from Bluenote competitors and alternatives in order to make an informed decision for your business.
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RegDesk
RegDesk
With the ever-increasing complexity of global medical device registration regulations, more companies are turning to regulatory information management systems software (RIMS software) to streamline the application life cycle and manage medical device applications. RegDesk is the most comprehensive AI-enabled RIMS platform for Medical Devices, Pharmaceuticals, and IVD companies offering enhanced performance and positive results more consistently than any standard regulatory information management solution. Our capabilities are as follows: • AI Application Builder • Regulatory Intelligence • Change Assessment • Standards Management • Country-Specific Templates • Distributor Collaboration • AI Document Management • Tracking & Reporting • Alerts and Notification • Product Management • Claims Management • EUDAMED For more information, visit our website. -
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Lockbox LIMS
Third Wave Analytics
A sample tracking, test result capture, and inventory management cloud LIMS for life science research, biotech/NGS, and industrial QC labs. Includes regulatory support for CLIA, HIPAA, Part 11, and ISO 17025. Nothing is more critical to a lab’s success than the quality, security, and traceability of samples. The Lockbox LIMS system provides robust sample management functionality to laboratory professionals, giving them full visibility on every aspect of a sample’s journey, from accessioning to long-term storage. LIMS analysis is about more than just tracking results- Lockbox’s multi-layered sample storage and location management functionality allows you to define your lab’s storage framework using a variety of location options: rooms, storage units, shelves, racks, boxes, and positions. -
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Xybion LIMS
Xybion
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. -
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Edison Analysis
Edison Scientific
Edison Analysis is a next-generation scientific data-analysis agent built by Edison Scientific. It is the analytical engine underpinning their AI Scientist platform, Kosmos, and it’s available both on Edison’s platform and via API. Edison Analysis performs complex scientific data analysis by iteratively building and updating Jupyter notebooks in a dedicated environment; given a dataset plus a prompt, the agent explores, analyzes, and interprets the data to provide comprehensive insights, reports, and visualizations, very much like a human scientist. It supports execution of Python, R, and Bash code, and includes a full suite of common scientific-analysis packages in a Docker environment. Because all work is done within a notebook, the reasoning is fully transparent and auditable; users can inspect exactly how data was manipulated, which parameters were chosen, how conclusions were drawn, and can download the notebook and associated assets at any time.Starting Price: $50 per month -
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Syntropy
Syntropy
Syntropy is a secure cloud-native platform built for healthcare and life sciences organizations to integrate, harmonise, analyse, and optimise complex biomedical and clinical data. It offers a unified environment where internal silos and external collaborations can converge, enabling data orchestration with purpose-based access control, full provenance tracking, and granular governance. It supports end-to-end pipelines, from data intake and ingestion, through semantic mapping and harmonization, to advanced analytics and workflow automation, enabling researchers, clinicians, and partner organizations to derive insights from rich compound datasets while preserving source integrity. Syntropy emphasizes transparency, attribution, and secure collaboration: data owners retain control over sharing, every action is audited and attributed, and the system is compliant with regulatory frameworks such as HIPAA, GDPR, and GxP. -
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Bigdata
Bigdata
Bigdata.com is an AI-driven financial research and intelligence platform that powers purpose-built AI agents and automated workflows for investment professionals, analysts, and developers to monitor markets, analyse trends, and extract actionable insights from vast, premium financial data in real time. It unifies premium data sources, including real-time news, regulatory filings, transcripts, market sentiment, structured financials, and alternative datasets into a searchable ecosystem that supports deep research, portfolio monitoring, and thematic analysis with full traceability back to original sources. Users can interact with intelligent research agents that perform multi-step analysis across all content, customise or build their own AI agents, automate repetitive research tasks such as watchlists, earnings previews, and sector breakdowns, and integrate via API to embed reliable, grounded financial intelligence into internal systems and models. -
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SciSpace BioMed Agent
SciSpace
SciSpace BioMed is a domain-native AI “co-scientist” for biomedical research that combines a vast literature database with 150+ integrated bio-tools and 100+ academic databases and software suites to streamline complex research workflows, from genomics and single-cell analysis to drug discovery and clinical genomics. It enables researchers to ask natural-language questions, ingest datasets, interpret variants or multi-omics data, design cloning or wet-lab workflows, reason about clinical or disease biology, and generate publication-ready outputs (e.g., figures, tables, and presentations) with full transparency and citations. Users can interact with scientific papers via “chat with PDF,” highlight confusing text, math, or tables, and get clear explanations, ideal for understanding difficult methods or concepts. For literature review or exploratory research, its AI-driven semantic search accesses millions of papers and returns citation-backed summaries.Starting Price: $12 per month -
8
RIMTrack
WinWire Technologies
With ever-changing national regulations, data standards, and complexities around preparing for regulatory submissions, regulatory affairs organizations in the healthcare and life sciences industry are convinced and driven towards smarter processes and intelligent systems to optimize costs, maximize accuracy and minimize timelines for the submission. Addressing the concern, regulatory information management, RIMTrack, is a cloud-ready artificial intelligence (AI) based new age regulatory information management system. It’s developed from scratch with the mission to help organizations to prepare submissions accurately and efficiently and by streamlining the regulatory processes related to tracking, licensing, approvals, regulatory and competitive intelligence, clinical trials, and reporting across global sites and stakeholders. Integrate with existing RIM system and achieve complete end-to-end management of regulatory life cycle process. -
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Veeva Vault RIM
Veeva
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. -
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Kalypso Accel for RIM
Kalypso
Kalypso provides life sciences companies with a cost-effective accelerator for a RIM system implementation - Accel for RIM. The solution enables an integrated platform to effectively manage and track product registrations, accelerate and improve the submissions accuracy, manage global UDI information, and enable efficient product distribution. It consolidates compliance and quality data from various enterprise solutions into a global source of truth for product registrations and tracking to accelerate regulatory submissions. Deployed using modern APIs to aggregate product data, regulatory documentation and submission packages. Pre-configured for rapid implementation with a validated software system. Based on industry-leading RIM practices and implementations. -
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FutureHouse
FutureHouse
FutureHouse is a nonprofit AI research lab focused on automating scientific discovery in biology and other complex sciences. FutureHouse features superintelligent AI agents designed to assist scientists in accelerating research processes. It is optimized for retrieving and summarizing information from scientific literature, achieving state-of-the-art performance on benchmarks like RAG-QA Arena's science benchmark. It employs an agentic approach, allowing for iterative query expansion, LLM re-ranking, contextual summarization, and document citation traversal to enhance retrieval accuracy. FutureHouse also offers a framework for training language agents on challenging scientific tasks, enabling agents to perform tasks such as protein engineering, literature summarization, and molecular cloning. Their LAB-Bench benchmark evaluates language models on biology research tasks, including information extraction, database retrieval, etc. -
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Sapio Sciences
Sapio Sciences
Sapio Sciences delivers the Sapio Platform, an agentic AI lab informatics platform that makes life in the lab easier and more productive for scientists. The unified, configurable, low code and scalable environment brings together Sapio LIMS, the market’s most advanced and flexible LIMS for automating research, diagnostics and manufacturing, Sapio ELaiN, the third generation AI lab notebook and scientific co scientist, and Sapio Scientific Data Cloud, the scientific data unification solution with built in organization, search, charting, tools and AI. Biopharma R&D, biotech, CRO and clinical diagnostics organizations use Sapio to run complex workflows and keep samples, experiments and data connected in one place instead of juggling disconnected systems. -
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Ennov RIM
Ennov
Imagine all of your regulatory information regarding products, registrations, submissions, correspondence and commitments in one centralized place accessible from anywhere. With Ennov RIM, life sciences companies can streamline their regulatory processes, improve their data quality, quickly answer business-critical questions and effectively respond to health authority requests. Ennov RIM is a purpose-built application (based on Ennov Process) for the management and tracking of therapeutic product details and registration information. Whether you are planning the launch of a new product or handling variations to existing registrations, Ennov RIM provides Regulatory personnel with the key information and functionality to effectively manage your product portfolios worldwide. -
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Ennov Regulatory Suite
Ennov
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. -
15
Claude for Life Sciences
Anthropic
Claude for Life Sciences is an AI-powered research platform developed by Anthropic, tailored explicitly for life sciences workflows such as drug discovery, experimental design, and regulatory documentation. The solution connects Claude’s large-language-model capabilities with key research environments and data sources, linking to platforms like lab information systems, genomic analysis tools, and biomedical databases, so scientists can move seamlessly from hypothesis generation through data interpretation to publication-ready outputs. The system also introduces “skills” and specialized connectors built for life-science use cases; for example, a skill for single-cell RNA-seq quality control, or integration with spatial-biology toolchains, enabling meaningful dialogue with analytic pipelines rather than simply raw prompts. By embedding into existing workflows, it reports performance that exceeds human baseline on protocol comprehension tasks, supports natural-language queries. -
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Agatha
Agatha
Agatha offers a suite of cloud-based applications tailored to the life sciences industry, enabling centralized management of documents and processes across clinical operations, quality, regulatory, and training functions. It supports biotech, pharmaceutical, medical-device, and contract-research-organization workflows by offering modules such as eTMF (Inspection-Ready Master Trial File), Remote ISF (Investigator Site File) management, SOP creation and approval, Quality document management for CAPAs, deviations, and change controls, and regulatory document management. Agatha enables streamlined document creation, review, approval, storage, and sharing in one unified system, supports paperless transformation to reduce administrative burden and strengthen data security, and is built on a global-compliance architecture addressing standards like 21 CFR Part 11, GDPR, and EU Annex 11. -
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Cayva.ai
Cayva.ai
Cavya.ai streamlines the setup phase of translation and localization projects by automating glossary creation, style guide generation, and document analysis. Its glossary generator extracts company names, acronyms, product terms, and technical vocabulary from any document, presenting each term with surrounding context and translations across 120+ languages. The style guide creator automatically crafts translation guidelines, covering tone, formatting, punctuation, measurements, dates, brand names, and more, tailored to each document and target language. Cavya’s smart document analyzer assesses content structure, complexity, and audience, assigns a translation difficulty score, flags compliance or regulatory risks, and recommends the ideal translator profile and project workflow. The tool supports bulk file uploads in 15+ formats (e.g., DOCX, PDF, JSON, XLIFF), delivers editable outputs, and ensures data privacy via end-to-end encryption and no AI training on user documents.Starting Price: $10 per month -
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ConcertAI
ConcertAI
ConcertAI is a leading provider of AI-powered solutions in the healthcare industry, specializing in oncology. Their mission is to accelerate insights and improve outcomes for patients through leading real-world data, AI technologies, and scientific expertise. ConcertAI offers a suite of products and services designed to enhance clinical research and patient care. Their Real-World Data Products provide comprehensive, fit-for-purpose datasets that support a variety of research needs across the enterprise. The digital trial solution streamlines clinical trial processes, while the Clinical Trial Optimization (CTO) platform utilizes large-scale AI to refine trial design and execution in oncology and hematology. In collaboration with NeoGenomics, ConcertAI has developed CTO-H, a SaaS solution focused on hematological malignancies, offering advanced research analytics and operational optimization. -
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FactoryTalk PharmaSuite
Rockwell Automation
FactoryTalk® PharmaSuite is the leading MES solution developed specifically for the Life Sciences industry. It provides role-based optimization of each stage of the recipe life cycle and drives time to results for all users. Its open-content architecture paired with an intelligent upgrade engine provides a powerful system for growth in both batch and discrete processing. Our FactoryTalk PharmaSuite MES provides value-based applications to help you adhere to regulatory compliance guidelines. MES also helps you achieve operational excellence, increase the effectiveness of your supply chain, and meet your sustainability goals. PharmaSuite MES provides production operations management to help you meet regulatory compliance, achieve operational excellence, increase supply chain effectiveness, and meet your goals. Optimize production, speed time-to-market, and ease compliance with a modern MES. -
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Redica
Redica Systems
Redica is an intelligence cloud platform designed to support quality and regulatory teams within life sciences organizations. It transforms complex global regulatory data into clear, actionable intelligence that helps teams stay compliant and proactive. The platform unifies regulatory intelligence, inspection findings, and supplier quality insights into a single connected system. By using explainable AI, Redica enables teams to monitor regulatory changes and understand their impact faster. Its inspection intelligence tools help organizations predict and prepare for audits using global benchmarking data. Redica also provides site and supplier intelligence to manage manufacturing and supply chain risks effectively. Overall, the platform shifts teams away from manual data tracking toward faster, insight-driven compliance decisions. -
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BIOVIA ONE Lab
Dassault Systèmes
BIOVIA ONE Lab is a comprehensive laboratory informatics solution designed to streamline workflows, enhance collaboration, and accelerate research across various scientific domains. It provides a unified environment for managing all laboratory data and processes, enabling scientists to make better decisions faster. ONE Lab is leveraged by companies across multiple industries, including Life Sciences, Consumer Packaged Goods, Energy & Materials, and more. It can be deployed across Research, Development, and QA/QC, with the flexibility to meet the specific needs of scientists in each domain. It manages samples, experiments, data, inventory, equipment, and workflows, integrating with a wide range of laboratory instruments and software to connect existing systems and data seamlessly. ONE Lab removes artificial barriers between ELN, LIMS, LES, equipment integration, and inventory management by employing a single data model across all functional areas. -
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RegDocs Connect
Montrium
RegDocs Connect gives your operational and regulatory teams the tools they need to prepare complete and compliant submission ready documents and records. Built with the end user in mind, collaboration, automation and quality are the foundation of this solution. Automated workflows manage your records lifecycle from draft to final, enabling your team to be in complete control of your regulatory documents at all times. Mapping of document types to the EDM reference model and eCTD facilitates organization and retrieval of documents for inclusion in regulatory submissions. Proprietary tools such as PDF/A Publishing, document classification, and unique document identifiers provide a powerful regulatory document management solution that pulls information from across your organization, into one manageable solution. With the rise of electronic submissions to regulatory agencies and the increased complexity of drug development, the ability to produce submission-ready, quality content -
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AssurX
AssurX
The AssurX platform is a versatile enterprise quality management system (EQMS) and regulatory compliance management platform. AssurX allows enterprises of any size or complexity to create a system that reliably communicates and coordinates quality and compliance information, documentation, and activities across the enterprise. AssurX allows regulated businesses to quickly identify and control risk exposure and avoid quality or noncompliance problems while improving workflow. AssurX QMS software is highly 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. Begin with just the solutions and functionality you need now, then implement what you like whenever you’re ready. No other system is easier to deploy, configure, and modify. -
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MonQual
MonQual
MonQual QMS comes with pre-built, DMS and LMS systems. But do you know it offers integration with various stand-alone systems too? You can integrate your LIMS (Laboratory Information Management System), MES (Manufacturing Execution System), SAP, WMS (Warehouse Management System), etc. This applies for both legacy and modern applications. MonQual is everything your quality team dreams of. It combines quality with compliance management, business intelligent tools, and business productivity. A built-in DMS and LMS services along with automated workflows takes care of your documents and regulatory standards. Quality deviations are a part of process; however, we can stop avoid them in the future. MonQual offers processes that can identify deviations at an early stage, tracks them and runs a root cause analysis and finally, records and documents them to avoid future recurrence. -
25
CINCO
Cinco
A web based software that uses Quality Risk Management to organize, analyze and trace Quality information directly to the specific risk it represents to the patient and drug product. Why Us? CINCO, a risk-based quality management software for the Life Sciences Industry. It provides paperless traceability of every critical to quality aspect of a drug or medical device to enable transparent quality decisions at every moment. Why Risk Management? Quality Risk Management is methodology that provides an objective approach into identifying and mitigating the risks of a drug or medical device manufacturing process. It is currently required by most regulatory agencies. However, the paper-based approach the Life Sciences Industry currently uses its ineffective in managing the significant and valuable risk data. It is prone to errors, introduces too much friction to the users and ends up not adding the potential value to the operations. On-demand access to what is critical to the product qua -
26
Signals Research Suite
PerkinElmer Informatics
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. -
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Flatiron Horizon
Flatiron
Flatiron Health's Evidence Solutions offer a flexible approach to generating both prospective and retrospective real-world evidence, empowering life sciences companies to achieve their oncology research goals more efficiently. Central to these solutions is Flatiron Horizon, which integrates a vast repository of over 5 million de-identified patient records and 1.5 billion data points, advanced curation methods, and disease-specific machine-learning models. This platform supports various stages of the biopharma lifecycle, including discovery, clinical study design, regulatory submissions, and post-marketing commitments. Flatiron's services encompass real-world data configurations tailored to specific oncology needs, prospective evidence generation through low-interventional studies, protocol optimization, patient identification, and seamless EHR-to-EDC data transfer via Flatiron Clinical Pipe. -
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Claude for Healthcare
Anthropic
Claude for Healthcare is a HIPAA-ready AI platform built on Anthropic’s advanced Claude models that helps healthcare organizations move faster without sacrificing safety, accuracy, or compliance by connecting to trusted medical, payer, and clinical data sources. It enables use cases such as prior authorization review, insurance claims appeals, clinical documentation generation, patient message triage, care coordination, and other administrative workflows by validating provider credentials, medical codes, coverage requirements, and drafting recommendations or summaries with traceable sources for verification. Claude can integrate with industry standards and databases, including CMS coverage policies, ICD-10 codes, provider registries, and PubMed, and supports secure connection to personal health records (e.g., lab results and medical histories) with user consent so patients or clinicians can get plain-language summaries and insights.Starting Price: $17 per month -
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Signals Translational
PerkinElmer
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. -
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Loftware Cloud Clinical Trials
Loftware
Loftware Cloud Clinical Trials is a comprehensive labeling and booklet management solution designed for the clinical trials industry. This platform helps streamline the creation, approval, and distribution of clinical trial labels, ensuring strict compliance with regulatory requirements such as FDA, EMA, and ICH. Loftware offers a centralized solution that manages labeling operations across global clinical trials, reducing errors, ensuring consistency, and improving overall efficiency. The software supports customizable templates, barcode generation, and integration with other systems to provide a seamless workflow throughout the clinical trial process. -
31
BenevolentAI
BenevolentAI
BenevolentAI is an AI-enabled drug discovery platform and scientific technology company that unites advanced artificial intelligence, machine learning, and domain-specific science to accelerate the discovery, design, and development of new medicines for complex diseases by making sense of vast, diverse biomedical data and generating actionable scientific insights faster than traditional methods. Its proprietary Benevolent Platform ingests and harmonizes structured and unstructured biomedical information, including literature, genomics, clinical information, and multi-omics data, into a comprehensive knowledge graph, enabling scientists to reason across biological systems, generate hypotheses, predict novel drug targets, and design candidate molecules with higher confidence and lower failure rates. -
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Norm Ai
Norm Ai
With deployments covering mission-critical workflows, Norm Ai understands the importance of regulatory compliance. Norm Ai agents empower compliance teams to access and implement the most comprehensive and up-to-date understanding of regulations, accelerating business outcomes. Risk and compliance challenges are evolving, placing stress on compliance teams to acquire new expertise. Norm Ai agents are constantly gaining new regulatory skills so you can benefit from an ever-expanding toolkit. Norm’s proprietary AI stack ensures unparalleled regulatory comprehension by our AI agents. Operating within networks of large language learning models, our AI Agents can make immediate compliance determinations, undertake complex multi-step tasks, and provide actionable feedback grounded in deep regulatory understanding. -
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Cytel
Cytel
Cytel is a leading global provider of clinical trial design software, biometric services, and advanced analytics, specializing in optimizing clinical trials and assisting pharmaceutical companies in unlocking the full potential of their clinical and real-world data. Founded in 1987 by distinguished statisticians Cyrus Mehta and Nitin Patel, Cytel has been at the forefront of adaptive clinical trial technology and biostatistical science. Our software solutions, including the East Horizon platform, empower precise trial design and simulation, utilizing adaptive and Bayesian tools to optimize protocols and accelerate drug development. The East Horizon platform integrates key components of Cytel's trusted software portfolio into a unified solution with R integration, enhancing trial design capabilities. Additionally, Cytel offers the Xact software suite, a comprehensive toolkit for statistical analyses of small datasets, and sparse, and missing data. -
34
Pepper Flow
Vodori
Pepper Flow’s unique features are built specifically to help life science companies streamline how marketing, medical, legal, and regulatory professionals work together. As a marketer, you need tools that allow you to move fast and keep things simple during advertising and promotional reviews. Get your critical campaigns and content to market to support your organization’s strategic initiatives. Maximize productivity by collaborating in real time to address feedback and turn around revisions. Spend less time managing the review process and more time on your high-priority to-dos. Pepper Flow is cloud-based, enterprise-grade software that enables life science companies to improve their competitive advantage, market products with efficiency, and maintain rigorous compliance. You need to move fast in order to deliver content to your key audiences. Pepper Flow’s intuitive interface allows you to get work done quickly and effectively. -
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AWS HealthOmics
Amazon
Securely combine the multiomic data of individuals with their medical history to deliver more personalized care. Use purpose-built data stores to support large-scale analysis and collaborative research across entire populations. Accelerate research by using scalable workflows and integrated computation tools. Protect patient privacy with HIPAA eligibility and built-in data access and logging. AWS HealthOmics helps healthcare and life science organizations and their software partners store, query, and analyze genomic, transcriptomic, and other omics data and then generate insights from that data to improve health and advance scientific discoveries. Store and analyze omics data for hundreds of thousands of patients to understand how omics variation maps to phenotypes across a population. Build reproducible and traceable clinical multiomics workflows to reduce turnaround times and increase productivity. Integrate multiomic analysis into clinical trials to test new drug candidates. -
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Scitara DLX
Scitara
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. -
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g.nome
Almaden Genomics
g.nome, a cloud-native platform that delivers streamlined, scalable, and interoperable workflows for next-generation sequencing analysis. g.nome provides a low-code/no-code pipeline build. With pre-built workflows and toolkits from a curated library, g.nome is giving power to researchers — enabling them to import custom code, handle big datasets reliably, and optimize team collaboration from anywhere. With g.nome, long-time barriers linked to workflow language, process flow visibility, and quality control are removed. All that’s left are streamlined, scalable, and interoperable genomic workflows — leaving research teams to do what they do best: focus on the science. -
38
Cruxi
Cruxi
Cruxi is a vertical AI platform built specifically for medical device regulatory teams. It ingests FDA regulations, guidance, product codes, standards, MAUDE events, recalls, and prior 510(k) data to power agentic workflows for 510(k), De Novo, and eSTAR. Users can run rapid device classification, compare predicates, plan evidence, and generate fully cited, eSTAR-aligned content for each subsection of the submission. Cruxi offers both full-submission workflows and focused micro-services (e.g., classification, predicate analysis, specific section drafting), making it ideal for early-stage startups, in-house regulatory teams, and consultants who want to deliver high-quality submissions with less manual work and fewer surprises from FDA.Starting Price: Credit-based system -
39
Teammately
Teammately
Teammately is an autonomous AI agent designed to revolutionize AI development by self-iterating AI products, models, and agents to meet your objectives beyond human capabilities. It employs a scientific approach, refining and selecting optimal combinations of prompts, foundation models, and knowledge chunking. To ensure reliability, Teammately synthesizes fair test datasets and constructs dynamic LLM-as-a-judge systems tailored to your project, quantifying AI capabilities and minimizing hallucinations. The platform aligns with your goals through Product Requirement Docs (PRD), enabling focused iteration towards desired outcomes. Key features include multi-step prompting, serverless vector search, and deep iteration processes that continuously refine AI until objectives are achieved. Teammately also emphasizes efficiency by identifying the smallest viable models, reducing costs, and enhancing performance.Starting Price: $25 per month -
40
Chematix
Chematix
The full-spectrum chemical management solution designed to meet the specific requirements and responsibilities of scientists, researchers, regulatory officials and administrators in education, government and industry. Comprised of modules to handle: Web Procurement of chemicals and supplies, complete life cycle chemical tracking, chemical inventory management and regulatory control, waste management and regulatory compliance, financial management and auditing, resource management and system security. On-line ordering process with shopping cart feature. Built-in product search feature accessing central stores, in-house stockrooms and major vendor catalogs: Fisher, Sigma Aldrich and VWR Scientific. The ability to track every on-site chemical to an exact location assistance with compliance with health and environmental regulatory guidelines. Chemical Abstract Database (CAD) to maintain data integrity. -
41
Affytrac
Affygility Solutions
Affytrac is our secure EHS software for the life science industry, currently in use at biotechnology, pharmaceutical and medical device companies throughout the world. As a web-based tool, there's no software to install, and with our streamlined setup process, there are no delays in having your EHS program automated, optimally tuned, and always at your fingertips. Simple and intuitive to use, yet powerful and full-featured, Affytrac includes all the functionality you expect in EHS software, without any unnecessary complexity to get in your way. Task Management lets you define your organization's set of compliance and safety tasks. Assign to personnel, add your target dates, and Affytrac automatically notifies staff and tracks progress. Document and track Corrective Actions identified through accidents, incidents, safety committees, regulatory inspections, and risk assessments. -
42
ZONTAL
ZONTAL
ZONTAL is a leading provider of digital solutions for the life sciences industry, specializing in streamlining laboratory operations and accelerating research outcomes through integrated analytics and data science. Their comprehensive platform offers a suite of products designed to enhance data management, including the Digital Lab for connecting data and experts, Data Preservation for safeguarding valuable information, and the Life Science Analytics Platform for integrating analytics into laboratory workflows. By ensuring data is Findable, Accessible, Interoperable, and Reusable (FAIR), ZONTAL empowers organizations to eliminate data wrangling, perform instant analyses, and unlock unlimited analytics potential, thereby transforming lab operations and fostering innovation in the digital age. -
43
IDBS Polar
IDBS
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. -
44
Verana Health
Verana Health
Verana Health is a real‑world data platform that transforms structured and unstructured electronic health record information into de‑identified, curated, disease‑specific data modules via its clinician‑informed and AI‑enhanced VeraQ population health data engine. Aggregating data from strategic partnerships with leading medical registries (including the American Academies of Ophthalmology, Neurology, and Urological Association), it encompasses over 20,000 clinicians and roughly 90 million patient records, providing near real‑time, high‑quality datasets to power real‑world evidence generation, clinical trial site and subject identification, clinician quality reporting, and medical registry management. Accessible through cloud services such as AWS Data Exchange and Amazon Redshift, the platform offers self‑service API access, an intuitive dashboard, and customizable cohort discovery tools, while advanced AI/ML algorithms, robust data quality assessments. -
45
LifeSphere NavaX
ArisGlobal
LifeSphere NavaX is your gateway to a future where advanced automation, AI, and intelligent data analytics converge to revolutionize your business and drive better end-to-end outcomes. LifeSphere NavaX is designed with scalability and customization in mind. We partner with you to map your automation journey based on your objectives, goals, and timeline. Stay in control with the ability to activate or deactivate features as needed. LifeSphere NavaX enhances LifeSphere solutions, seamlessly integrating with third-party systems to ensure a smooth transition to a more intelligently automated future. LifeSphere NavaX is developed in collaboration with pharmaceutical and regulatory leaders, maintaining the highest levels of quality and security through robust governance frameworks and compliance standards. Automate routine manual workflows and processes for unmatched end-to-end time and cost savings, including up to 50% efficiency gains on key workflows. -
46
ZAIDYN
ZS
ZAIDYN is an AI-powered, cloud-native platform developed by ZS to revolutionize the life sciences industry. It integrates advanced analytics, machine learning algorithms, and intelligent workflows to empower organizations in transforming processes across research and development, commercialization, and patient engagement. The platform's modular design allows for scalable solutions tailored to specific needs, facilitating seamless integration with existing IT infrastructures through its open architecture. ZAIDYN enhances cross-functional collaboration by providing unified, high-quality data and insights, thereby reducing operational silos and promoting informed decision-making. With a focus on security and compliance, the platform ensures data privacy and adheres to regulatory standards, making it a reliable choice for life sciences companies aiming to innovate and improve health outcomes. -
47
ComplianceAuthor
Glemser Technologies
Glemser provides IT solutions for regulated industries with a focus on global life sciences and the ecosystem that improves patient outcomes. ComplianceAuthor makes it seamless for life science companies to manage global product labeling, provide affordable IDMP and reduce compliance risk. ComplianceAuthor for Global Labeling helps life science regulatory professionals manage, scale, and streamline global product labeling and compliance through artificial intelligence, structured content, and natural language generation. Artificial intelligence and machine learning to find, index and derive knowledge needed to recommend your next best course of action. Our workflow overlays provide innovation for process standardization, resulting in components that are compliant and controlled. Natural language generation enables you to adopt operational efficiencies and smarter automation. -
48
Veeva Vault
Veeva Systems
Bridging content gaps across the enterprise for global harmonization, while supporting local autonomy. Veeva Vault is a true cloud enterprise content management platform and suite of applications specifically built for life sciences. Traditionally, companies have had to deploy applications for content and separate applications to manage associated data. Veeva Vault is the only content management platform with the unique capability to manage both content and data. Companies can now eliminate system, site, and country silos and streamline end-to-end processes across commercial, medical, clinical, regulatory, quality, and safety. Because all Vault applications are built on the same core platform, companies gain additional efficiency and compliance through the streamlined flow of documents across regions and departments. Content stays accessible, current, and in context across the entire development and commercial lifecycle. -
49
cubeSAFETY
CRScube
cubeSAFETY is a pharmacovigilance platform built to help safety teams manage adverse-event reporting, regulatory submission and case processing in a compliant, efficient workflow. The system supports ICH E2B and regional reporting standards, enables submissions to FDA, EMA, CDE, MFDS and PMDA via dedicated gateways, and automatically translates and formats data for CIOMS and XML export. It includes AI-powered medical-coding suggestions, duplication-detection, import of CIOMS PDF files, real-time submission-tracking dashboards, and full integration with other CRScube modules such as cubeCDMS. The platform is designed to streamline safety-case entry, ensure high data quality through built-in validation, and simplify workflows for global regulatory compliance while reducing manual burden and budget overhead. -
50
MyCalPharm
Infokart India Pvt. Ltd.
MyCalPharm is an advanced animal-simulated pharmacology teaching software designed to enhance learning and experimentation in the field of pharmacology. Developed by Infokart India Pvt. Ltd., MyCalPharm provides an ethical, cost-effective, and interactive alternative to live animal experiments, aligning with modern educational and regulatory standards. Our Features: Tutorial and Examination Modes Seamless Evaluation System Feedback & Suggestion System Faculty Monitoring Support Chat
