Alternatives to Pristima
Compare Pristima alternatives for your business or organization using the curated list below. SourceForge ranks the best alternatives to Pristima in 2026. Compare features, ratings, user reviews, pricing, and more from Pristima competitors and alternatives in order to make an informed decision for your business.
-
1
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. -
2
STARLIMS
STARLIMS
We simplify the complexity of your entire product lifecycle management process. Easy-to-use and adaptable to your organization’s needs, the STARLIMS brand of lab informatics solutions support the rapidly changing data management needs across your organization. Our laboratory information management solutions (LIMS software) can integrate with your current systems, while also identifying opportunities to improve processes so you can bring high quality and safe products to market faster. -
3
BIOiSIM
VERISIMLife
BIOiSIMTM is a first-in-class 'virtual drug development engine' that offers unprecedented value for the drug development industry by narrowing down the number of drug compounds that offer anticipated value for the treatment or cure of specific illnesses or diseases. We offer a range of translational-based solutions, customized for your pre-clinical and clinical programs. These offerings are all centered around our proven and validated BIOiSIMTM platform for small molecules, large molecules, and viruses. Our models are built on data from thousands of compounds across 7 species, leading to robustness rarely seen in the industry. With a focus on human outcomes, the platform has at its core a translatability engine that transforms insights across species. The BIOiSIMTM platform can be used before the preclinical animal trial start, allowing earlier insights and savings in expensive outsourced experimentation. -
4
Savante
Xybion Corporation
Consolidating and validating data sets is a highly challenging and business-critical effort for many Contract Research Organizations (CROs) and drug developers who perform toxicology studies either internally or outsourced with external partners. Savante provides a mechanism for your organization to create, merge, validate, and visualize preclinical study data regardless of source or format. Savante provides a vehicle for preclinical data aggregation, analysis, and visualization in SEND format to scientific staff and management. Preclinical data from Pristima XD is automatically synchronized into the Savante repository. Data from other sources can be aggregated through migration and import, including direct loads of sent data sets. The Savante toolkit handles the necessary consolidation, study merging, control terminology mapping, and data definition file preparation. -
5
Clindata Cloud
Clinical Data
Clindata Cloud receives pre-clinical / clinical / Risk Metric data from multiple data sources/sites, and empowers the clinical operations teams, with submission-ready data sets, analytics and risk-based monitoring alerts. Consolidate & harmonize study data from multiple data sources into a comprehensive study data model. Validate received data for completeness, accuracy, integrity and consistency and raise alerts and notifications in case of exceptions or risk patterns. Standardize data to CDISC data standards, to eliminate noise and create submission-ready data sets in real-time for continuous validation of data & analysis. Generate submission-ready analytics in real-time based on standardized data. -
6
Metabolon
Metabolon
At Metabolon, we offer the largest Level 1 library in the metabolomics industry. Our proprietary library has been built and curated over 20 years and contains over 5,400 entries. The vast majority of entries in our library are Level 1 attributing approximately 85% (~4,600 entries); however, some are Level 2 (approximately 15% accounting for around 800 entries) due to a lack of commercial standards available to qualify for Level 1. Metabolon delivers accurate, highly actionable insights for our clients’ scientific or clinical inquiries due to our unmatched library breadth and industry-leading annotation confidence levels. Metabolomics applies to a wide range of research, from soil health to food nutrition and preclinical research to clinical trials. Whether you’re searching for trends in a group or refining an individual’s treatment, metabolomics can help you find answers to important questions. -
7
Phoenix PK/PD Platform
Certara
With all the tools you need in a single, interoperable platform, effortlessly share pre-clinical and clinical knowledge across your organization through secure and consistent workflows using Phoenix-based tools and 3rd-party applications. Phoenix WinNonlin is the first choice for non-compartmental analysis (NCA), toxicokinetic modeling, and pharmacokinetic and pharmacodynamic (PK/PD) modeling by over 6,000 researchers at biopharmaceutical companies, academic institutions, and 11 global regulatory agencies, including the US FDA, EMA, PMDA and more. The Phoenix Platform also features population PK/PD (popPK) modeling with Phoenix NLME and Level A correlation via the Phoenix IVIVC Toolkit, Validation Suites provide fast and easy software validation in under 30 minutes. -
8
Seralogix Study Manager
Seralogix
An integrated suite of professional products, enabling you to dynamically share pre-clinical study data across an enterprise and around the world, with cutting-edge functionality, and industry-embraced standards. Seralogix Study Manager™ is a new platform aiming to standardize and streamline pre-clinical studies via an elegant interface. Suitable for individual researchers and scalable to vast research enterprise, the platform employs sophisticated computing power to make your experimental design, data collection, and reporting a breeze. This suite of tools will enable you and your team to have confidence in your data quality and enjoy the benefits of instant reporting. Correctly planning your experimental design can be a daunting task. Seralogix Study Manager walks you through the process of experimental design to achieve the statistically rigor necessary to ensure your studies success. -
9
PharmaPendium
Elsevier
PharmaPendium is a comprehensive resource that provides access to FDA and EMA drug approval documents, including pharmacokinetic, pharmacodynamic, and safety profiles. It offers detailed information on drug-drug interactions, adverse effects, and clinical study outcomes, facilitating informed decision-making in drug development and regulatory submissions. The platform's extensive data supports researchers and healthcare professionals in evaluating drug efficacy and safety, contributing to the advancement of pharmaceutical research and patient care. Find information about previous regulatory submissions and profit from precedents to predict agencies’ requirements. Seamlessly move from table view to interactive charts, graphs, and visual aids to easily interrogate and interpret data. Find information by adverse events (MedDRA), targets, indications, drug,s and endpoints using normalized data. Result pages bridge the preclinical to clinical divide. -
10
Cortellis
Clarivate
Unlock hidden insights in data using the Cortellis™ suite of life science intelligence solutions – so you can make better informed decisions along the entire R&D lifecycle. We’ve removed the hard work of finding, integrating, and analyzing data so you can focus on the critical decisions needed to get your products to market faster. Applying a unique depth, breadth and quality of data that is enriched with deep domain knowledge, industry understanding, and therapeutic expertise, Cortellis unlocks hidden insights to drive data-driven decisions that accelerate innovation. Get precise, actionable answers to your specific questions across the R&D lifecycle with the broadest and deepest sources of intelligence. Accelerate innovation with Cortellis as an indispensable part of your daily workflow. -
11
Pluto
Pluto Biosciences
Since its founding in 2021 from the Wyss Institute at Harvard University, Pluto has become a trusted partner of life sciences organizations around the country ranging from biotech start-ups to public biopharma companies. Our cloud-based platform gives scientists the ability to manage all of their data, run bioinformatics analyses, and create interactive and publication-quality visualizations. The platform is currently being used for a wide variety of biological applications, from preclinical / translational science research, to cell and gene therapies, drug discovery and development, to clinical research. -
12
Clinisys Laboratory Platform
Clinisys
HORIZON is now Clinisys, the number one provider of laboratory information systems across the globe. Clinisys brings together laboratory information system expertize across the globe to offer flexible laboratory solutions across healthcare, environment, toxicology and public health, pharma and biotech. The full capabilities of HORIZON LIMS now form the basis of the Clinisys Laboratory Platform a robust, affordable, data-centric software platform built to configure and integrate with every kind of lab. HORIZON LIMS is now known as Clinisys Laboratory Platform and meets the needs of a wide variety of lab challenges. From the samples you test to the way you operate, each lab has unique features that make them great at what they do. Clinisys Laboratory Platform configures to suit and integrate specifically with your lab. HORIZON LIMS is now known as Clinisys Laboratory Platform and meets the needs of a wide variety of lab challenges. -
13
Curi
Curi Bio
Mantarray brings functional data into the earliest stages of preclinical testing of new medicines. By providing parallel analysis of 3D engineered muscle tissues with adult-like functional profiles, Mantarray enables the discovery, safety, and efficacy testing of new therapeutics. With over 95% tissue formation success rate, the Mantarray Plate Kit allows for reliable and reproducible engineered tissues across 24 wells. The Mantarray platform provides an easy-to-use, scalable, and flexible system that allows researchers to examine 3D tissues in vitro in the convenience of their own lab. Be among the first to receive the instrument. The Mantarray system features a novel magnetic sensing technique that can detect the contraction of EMTs. This enables the user to measure the contractility of 24 tissues in parallel, a high throughput, and in real time. The system features user-friendly software that takes away the requirement for manual calculations of contractility. -
14
Chemia
Laurus Infosystems
Chemia is a Browser-based & cloud-ready ELN platform. Chemia is conceived, designed and architected by scientists for scientists. A platform to drive, assign, manage and monitor all R&D activities and record capture from one dashboard. It enables you to automate your R&D set-up and make it a truly paperless operation. It saves time(approx. an hour saved per scientist) with Cross-functional collaboration; makes you audit-ready and manages data effectively. Quick retrieval, search, comparative study, and reconfigurability enable faster and appropriate decisions. An inventory management system that organizes, maintains and schedules relevant information for chemicals and equipment used inside the laboratory. A system that provides usage logs of equipment, maintenance logs and calibration logs, for effective management of labs and efficient working. A system that provides the protocol and adherence to it for compliance. -
15
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. -
16
Patholytix
Patholytix
Through strong relationships with the leading CROs, we offer an alternative strategy for the secure onboarding and review of studies. Our superior ergonomics in study management and image review along with integrated AI, significantly improves the efficiency of our pathologist users. Revolutionary cloud-based infrastructure allowing on-demand collaboration between remote Pharma and CRO partners from any location around the world. Complete control over the structure of your studies, supporting any type of associated data, study size, and WSI vendor format, including SEND data representation and LIMS integration capabilities, within a simple, intuitive interface. Offering a blend of workflow design, viewing performance, and ease of use that delivers a truly unique digital pathology experience. Patholytix Preclinical is a fully scalable solution that grows in line with your organizational needs, ensuring on-demand access to studies from the office or at home. -
17
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. -
18
LabRelations
LabRelations
LabRelations is a modern, configurable laboratory platform built to centralize and streamline scientific and test workflows by combining core modules, including LIMS (Laboratory Information Management System), ELN (Electronic Lab Notebook), CTMS (Clinical Trial Management System) and EDC (Electronic Data Capture), into a single system that supports everything from sample tracking and experiment documentation to study management and regulatory-grade reporting while reducing manual work, errors and data silos; it lets labs store all data in one place, define rule-based workflows and automations, connect instruments and external systems, enforce full audit trails and compliance (such as GxP, 21 CFR and versioned controls), and configure objects, forms, views and permissions to fit specific lab needs, while enabling cross-functional collaboration and real-time visibility from discovery and quality control to clinical research and complex regulated environments. -
19
BizNet
Sarjen Systems
Sarjen delivers an AI-enabled Clinical Trial Management System and Bioanalytical LIMS that drives digital transformation across early-phase and late-phase clinical trials. This integrated eClinical platform supports end-to-end trial management, site management, subject tracking, regulatory compliance, and real-time laboratory sample management within a unified ecosystem. Built for pharma, biotech, and CRO organisations, the software enhances operational efficiency through workflow automation, centralised data management, and advanced analytics. Its AI features include predictive enrollment forecasting, risk-based monitoring insights, anomaly detection in lab data, automated query resolution, and intelligent dashboards that improve decision-making. By leveraging machine learning and smart automation, the platform accelerates study timelines, improves data quality, ensures compliance readiness, and transforms clinical research operations!Starting Price: $79 -
20
Amira Software
Thermo Fisher Scientific
Thermo Scientific Amira Software is a powerful, universal 2D–5D solution for visualizing, analyzing, and understanding life science and biomedical research data from various imaging modalities, including optical and electron microscopy, CT, MRI, and other techniques. With incredible speed and flexibility, Amira Software supports advanced 2D–5D bioimaging workflows in research areas ranging from structural and cellular biology to tissue imaging, neuroscience, preclinical imaging, and bioengineering. Key features include import and image data processing, visualization and exploration, advanced segmentation, measurement, quantification, and analysis, as well as specialized tools for molecular visualization, object tracking, filament tracing, meshing for finite element analysis, diffusion tensor imaging, 3D registration, and biomaterial deformation analysis. Amira Software also offers customization options and access to ecosystems such as MATLAB, Python, and custom C++. -
21
Nautilus LIMS
Thermo Fisher Scientific
To accelerate new discoveries and get products to market as quickly as possible, R&D and manufacturing labs have to reconfigure and change on the fly. Data management can’t be a bottleneck. Developed in partnership with customers in fast-paced R&D environments, the Thermo Scientific™ Nautilus LIMS™ for Dynamic Discovery and R&D Environments is a highly flexible, easily configurable system that increases workflow efficiency, throughput and data reliability while simplifying administration, sample traceability and regulatory compliance. Automated handling of complex boards and proprietary graphics instruments make data monitoring and management easy, even novice users can delineate and track processes with ease. Clients can create workflows, delineate the life cycles of the samples and automate actions between different platforms while integrating regulated processes that comply with good laboratory practices and the 21 CFR Part 11 guidelines. -
22
Discngine Assay
Discngine
Discngine Assay is a laboratory informatics platform that integrates every phase of plate-based assays into a cohesive, compliant, and efficient workflow, making it an essential tool for screening research labs. It enables scientists to streamline the entire High Throughput Screening workflow, from sample management and assay data analysis to data warehousing and liquid handling equipment qualification. With its intuitive interface and robust API, Discngine Assay integrates seamlessly with Lab equipments and existing IT environment, ensuring efficient data capture and processing. Designed to accelerate new molecule discovery, it addresses the needs of pharmaceutical, biotech, and CRO industries, enhancing collaboration and driving innovation in life science research. -
23
Aiforia
Aiforia
Aiforia equips pathologists and scientists in preclinical and clinical labs with powerful deep learning and cloud-based technology to advance their image analysis tasks and workflows. From empowering researchers in the identification of novel biomarkers of disease, and supporting R&D scientists in speeding up the time-to-market of novel drugs, to helping pathologists enhance the accuracy of cancer diagnostics, Aiforia has the expertise and experience to transform healthcare all the way from discovery to diagnosis. For clinical pathology labs aiming to increase productivity and improve diagnostic accuracy, the Aiforia Clinical Suites offer a portfolio of tools for AI-supported diagnostics, intelligent visualization, QC, and automated pre- and post-screening. We are currently developing Suites for some of the world’s most prevalent cancers and have CE-IVD marking for AI models in lung and breast cancer. -
24
Kaleido
Kaleido
The microbiome is implicated in numerous diseases and health conditions. Learn how Kaleido is leading a differentiated approach to translating the promise of the microbiome into solutions for patients. The human microbiome is a community of more than 30 trillion microbes, organisms that include bacteria, viruses, archaea and fungi, which reside on and inside the human body. Over the last decade, research has increased exponentially on the impact the microbiome has on human health, including cardiovascular disease, cancer, diabetes, Parkinson’s disease and allergies. This highly complex microbial ecosystem has been referred to as a “newly discovered organ.” Many other human organs command tens of billions of dollars for therapeutics that treat disease by modulating physiology. From a therapeutic perspective, the microbiome organ remains a largely untapped frontier in healthcare. -
25
Cronos
Webosphere
In-system protocol & its a training program. Equipped with fingerprint attendance. Cronos provides highly customizable if/workflows capable for conducting derma/ patch/ other BA-BE/ early phase studies. Capture, cleanse and efficiently manage your study data from paper-based or EDC-based trials. Extract data in desired datasets following standards like CDISC (SDTM). EDC tool with real-time activities. It’s Bedside Data Collection capabilities help in paperless & faster assessments. It comes with a sample inventory & tracking facility as well. Compliance-ready data repository.The facility of data e-printing from almost all BA instruments/software and online review of data in defined workflow with e-stamping and e-signature.Project-wise view, export & archival of data. Generate high-quality statistical reports (tables, listings & formats) in fixed/desired formats with ease. -
26
PRA Prism
Nextrials
Data comes at you from all directions – EDC, EHR, smartphones, mobile devices, central laboratories. Prism assimilates data from these disparate sources and transmutes them into information and ultimately knowledge. Prism EDC combines ease-of-use with innovative features to provide a fresh solution for the collection and management of clinical trial data. Prism offers more that than form-based data collection, it aggregates and manages data from a myriad of data sources. Prism eSource is an innovative software solution that allows research teams to extract clinical trial information directly from a site’s electronic health record (EHR). This creates efficiencies and cost savings beyond the current paradigm where sites must enter the same data in multiple systems and accelerates the delivery of novel therapies to patients. -
27
3decision
Discngine
3decision® is a cloud-based protein structure repository designed for comprehensive structural data management and advanced analytics, enabling small molecule and biologics discovery teams to accelerate structure-based drug design. It centralizes and standardizes experimental and in-silico protein structures from public sources like RCSB PDB and AlphaFoldDB, as well as proprietary data, supporting formats like PDBx/mmCIF and ModelCIF. This ensures easy access to X-Ray, NMR, cryo-EM, and modeled structures, fostering collaboration and enhancing research efforts. Beyond storage, 3decision® enriches entries with metadata and sequence information, including protein-ligand interactions, antibody annotations, and binding site details. Advanced analytical tools identify druggable sites, assess off-target risks, and enable binding site comparisons, transforming vast structural data into actionable knowledge. Its cloud-based platform facilitates collaboration among research teams. -
28
TruLab
TruLab
We provide a truly end-to-end tracking solution for use in clinical trials. Simply download the software onto your trial managers’ mobile devices and sit back as TruLab’s blockchain technology does the rest. Don’t wait until samples reach a central lab to spot potential problems. Spot data anomalies in real-time as samples work their way through the clinical trial. TruLab allows for constant remote accessioning of samples. 20% of samples are lost or deemed unusable in late-stage trials. Ethically, logistically, and financially, this is unacceptable. Samples are no longer exclusively collected at clinical sites. The new world of collection at residences presents a host of novel sample-tracking problems. TruLab tracks samples wherever they are in the world, from residence to repository. -
29
MAISi
Agile Health Computing
Until now, the options available for managing clinical trials at an investigator site were either keeping multiple shared spreadsheets or buying expensive software unsuited to Australian conditions. MAISi is the game-changer. Beginning as a repository for clinical trials data at a major hospital in 2001, MAISi has evolved into a sophisticated workflow application to assist in most aspects of a research unit’s operations. MAISi acts as a central repository of data to store information about studies and the business units that run them. The datasets are arranged to support management decision-making. Staff in each business unit have access to the data (Studies, Patients, Investigators, Study Team Members) associated with their own business unit, whereas staff granted global access (normally Financial Officers and System Administrators) have access to all data. -
30
Causaly
Causaly
Leverage the power of AI to expedite the journey from bench research and laboratory insights to the launch of life-changing therapies. Gain up to 90% in research productivity by reducing your reading time from months to minutes. Cut through the noise with a high-precision, high-accuracy search to navigate the ever-growing volume of scientific literature with ease. Save time, reduce bias and increase odds of novel discoveries. Deeply explore disease biology and conduct advanced target discovery. Causaly’s high-precision knowledge graph consolidates evidence from millions of publications, making deep, unbiased scientific exploration possible. Rapidly navigate biological cause-and-effect relationships without being an expert. Get a view of all scientific documents and uncover hidden connections. Causaly’s powerful AI machine reads millions of published biomedical literature to support better decision-making and research outcomes. -
31
Healnet
Healx
Rare diseases are often not well studied and there is a limited understanding of many of the aspects necessary to support a drug discovery program. Our AI platform, Healnet, overcomes these challenges by analyzing millions of drug and disease data points to find novel connections that could be turned into new treatment opportunities. By applying frontier technologies across the discovery and development pipeline, we can run multiple stages in parallel and at scale. One disease, one target, one drug: it's an overly simple model, yet it's the one used by nearly all pharmaceutical companies. The next generation of drug discovery is AI-powered, parallel and hypothesis-free. Bringing together the key three drug discovery paradigms. -
32
Eidogen-Sertanty Target Informatics Platform (TIP)
Eidogen-Sertanty
Eidogen-Sertanty's Target Informatics Platform (TIP) is the world's first structural informatics system and knowledgebase that enables researchers with the ability to interrogate the druggable genome from a structural perspective. TIP amplifies the rapidly expanding body of experimental protein structure information and transforms structure-based drug discovery from a low-throughput, data-scarce discipline into a high-throughput, data-rich science. Designed to help bridge the knowledge gap between bioinformatics and cheminformatics, TIP supplies drug discovery researchers with a knowledge base of information that is both distinct from and highly complementary to information furnished by existing bio- and cheminformatics platforms. TIP's seamless integration of structural data management technology with unique target-to-lead calculation and analysis capabilities enhances all stages of the discovery pipeline. -
33
Clinical Ink
Clinical Ink
Get on the path to cleaner data and confident decisions with Clinical Ink. As the pioneers in eSource, Clinical Ink’s technology platform and delivery capabilities provide greater certainty from source to submission. Explore Lunexis™, a clear and connected eSource Ecosystem that delivers purpose-built data capture solutions for your protocol at the critical moments that matter. The Lunexis platform makes it easy to deploy an integrated, convenient eSource solution that provides anytime, anywhere access to your study data. We deliver more than fast, clean data — we deliver confidence. Not only are your sites and patients assured of an easier experience, but you can be certain that your patients are more compliant and engaged and that your protocol is executed correctly. Start your most complex studies with confidence — implement Lunexis to support well-informed, optimal decisions. -
34
Ennov CTMS
Ennov
Ennov CTMS facilitates the end-to-end management of clinical trials. The software allows sponsors to be more efficient, to make better decisions, to ensure compliance, to select investigators well, to monitor patient recruitment and to manage finances. Ennov CTMS includes comprehensive directories to manage site personnel (investigators, sub-investigators, study coordinators, pharmacists) and organizations (hospitals, competent authorities, CROs, suppliers). Ennov CTMS provides functions for tracking patients, patient visits, EDC data, activities, queries, deviations, adverse events, drug supply, monitoring visits and finances. A full complement of reports and dashboards provide total visibility into the status of each study, country, site and investigator to provide the information necessary to make the best decisions possible. - Comprehensive CTMS software - Integrated with Ennov Clinical Data Management - Clear visibility into investigational sites - Integrated workflow -
35
QuesGen Platform
QuesGen Systems
From simple turnkey solutions to large-scale multi-site studies, we help PIs overcome common obstacles and limitations with their database setup and selection. Researchers also hire QuesGen to advise on data management best practices and provide additional services where needed to help studies get up and running more quickly. Experienced partner for dozens of academic institutions and researchers. Experienced in managing large data sets and running data curation through our flexible data platform. The ability to set up and scale research initiatives quickly and easily. With a comprehensive data model, assessments library, and curation expertise, QuesGen gets you up and running quickly, and ensures quality, compliant data, so you can focus on the analysis of the results. Support multiple clinical research initiatives across your institution using HIPAA and FDA 21 CFR Part 11 compliant solutions that can integrate with your EMR, FITBIR (Federal Interagency TBI Repository.Starting Price: $100 per month -
36
Viewics
Viewics
We built Viewics to solve the challenge of making healthcare data meaningful. Our platform is safe and secure with the power to transform organizations. The Viewics Platform is an end-to-end healthcare analytics platform that surfaces actionable insights that empower you to improve patient care, operational effectiveness, and financial performance in your lab and across the healthcare continuum. Preconfigured alerts for common laboratory KPIs proactively notify users at important thresholds for increased transparency and control. Individually customized dashboards highlight only the most relevant data to ensure end-user comfort and continued use of the platform. Built-in workflows that promote participation, include sharable dashboards and annotations to enable actionable, data-driven insights. Analyze data, from multiple sources, that resides inside and outside of the laboratory environment. -
37
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. -
38
TrialStat
TrialStat Solutions
Compared to other EDC solutions on the market from MediData, DataTrack, Omnicomm and others, TrialStat is the most all-encompassing suite of study management tools that can be seamlessly connected to external data sources such as EMR, wearables, and other clinical and non-clinical data and information sources. TrialStat offers a fully unified platform suitable for all phases and types of trials. Our single-sign-on, multi-tenant EDC suite includes modules for Randomization, Adjudication, Coding, Safety, Patient Diaries/ePRO, Vendor Neutral Imaging Archive, a robust Reporting and Analytics Portal and custom Machine Learning programs. With a focus on data analytics, TrialStat offers real-time reporting, data extracts on demand, and analytics across a single study, a program, or your entire research portfolio – providing all stakeholders relevant, customized, timely insight into all aspects of study data and highlighting areas of risk or potential delays. -
39
DrugPatentWatch
DrugPatentWatch
Global biopharmaceutical drug patent and generic entry business intelligence. Anticipate future budget requirements and proactively identify generic sources. Assess past successes of patent challengers and elucidate research paths of competitors. Inform portfolio management decisions on future drug development. Predict branded drug patent expiration, identify generic suppliers, and prevent overstock of branded drugs. Obtain formulation and manufacturing information; identify final formulators, repackagers, and relabelled.Starting Price: $250 per month -
40
RealTime-CTMS
RealTime-CTMS
RealTime-CTMS is a premier, cloud-based clinical trial management system (CTMS) purpose-built to boost efficiency and profitability for site networks and research sites. Comes with fully-integrated services that include RealTime-PAY, RealTime-TEXT, and RealTime-eDOCS (the first fully-integrated eRegulatory document management system), the solution promotes quicker and easier access to subject or study information using simple and intuitive navigation. RealTime-CTMS offers a host of other solutions that covers online document storage, appointment reminders, data collection, payment processing, among others.Starting Price: $295.00/month -
41
Evidex
Advera Health Analytics
Automated surveillance of any data source, fully integrated with a GVP IX compliant signal management platform. GVP-IX compliant signal management platform integrated within Evidex and ready to use off-the-shelf. Modernize and audit-proof your management processes without having to move back and forth between platforms and services. Unlock the value of your safety data. When you automate signal detection and management, you can focus not just on regulatory requirements, but on driving value for your organization. Identify safety signals from traditional sources like ICSR databases, FDA Adverse Event Reporting System (FAERS), VigiBase and clinical trial data. Include new data sources such as claims, EHR, and other unstructured data. Bring these pools of information together seamlessly to enhance signaling algorithms, make validations and assessment more efficient, and provide faster answers to drug safety questions. -
42
Biorce Aika
Biorce
Biorce’s Aika is an AI-native clinical intelligence platform that accelerates every stage of the clinical trial lifecycle by replacing slow, manual protocol development and feasibility assessment with explainable, evidence-based automation. Built on insights from around one million real global trials, it generates first-draft study protocols, complete regulatory documentation, site feasibility assessments, risk and data management plans, and other essential trial artifacts in a fraction of the time traditional methods require, helping reduce delays and costly amendments. Aika provides full transparency into how it reaches recommendations so teams can confidently present choices to regulators and maintain expert control, blending AI speed with clinical expertise. It minimizes trial preparation timelines from weeks to days, cuts the number of amendments, and lowers overall risk while integrating seamlessly into existing workflows without heavy retraining. -
43
Datatrial Nucleus
Datatrial
One Platform to Research, Document, and Collate your Clinical Data. Simplify your research data with the Nucleus platform. A single platform to store your study documentation, clinical datasets, submission data and compliant media. Nucleus Documents enables document management and version control for your quality documentation and media. Control, manage, and share company content with ease. Collate and control your electronic trial master file documents with ease using our centralized regulatory document management solution. Nucleus Coding enables dictionary term coding against both MedDRA and WHODrug dictionaries, either in our standalone application, or integrated into your data capture system. -
44
Dotmatics
Dotmatics
Dotmatics is the global leader in R&D scientific software that connects science, data, and decision-making. Combining a workflow and data platform with best-of-breed applications, we offer the first true end-to-end solutions for biology, chemistry, formulations, data management, flow cytometry, and more. Trusted by more than 2 million researchers from the world’s leading biopharma, chemicals and materials enterprises, and academic institutions, we are dedicated to working with the scientific community to help make the world a healthier, cleaner and safer place to live. Learn more about our platform and products, including GraphPad Prism, Geneious, SnapGene, Protein Metrics, LabArchives, and more. -
45
Omda MedSciNet
Omda
Omda MedSciNet solutions improve the quality, utility, and management of medical data from collection to analysis. This secure standardized software makes it easy for clinical researchers and other professionals in medicine and academia to gather and analyze well-managed medical data. The Omda team specializes in building and managing tailor-made database applications and designing clinical studies for medical research and quality registers. The Omda MedSciNet study platform provides a reliable, feature-rich, and highly customizable online environment for hosting and managing sophisticated study and clinical trial systems. Omda MedSciNet has a 20-year track record of successfully hosting studies and clinical trials of all scopes and sizes. The standard implementation includes a comprehensive set of components necessary for establishing fully functional studies or clinical trials. -
46
uMotif
uMotif
uMotif is a modern eCOA/ePRO and eConsent platform designed to power clinical and real-world research. Developed in collaboration with patients, the platform delivers unrivaled engagement, transforming the speed, quality, and accuracy of data. By combining uMotif's eCOA/ePRO with continuous glucose monitoring data capture, the platform delivered unprecedented data compliance rates for a pan-European diabetes study. In an immunology study, the patient-centered eCOA/ePRO solution helped the sponsor complete data capture requirements six months early. In an FDA-required CNS study, participants were engaged to capture submission-ready ePRO through their own devices. uMotif has always designed for patients first, with a relentless focus on understanding the patient journey and what drives patient behavior. This deep knowledge allows the design of software that best meets the needs of patients and delivers exceptionally high levels of engagement to study sponsors. -
47
cubeCTMS
CRScube
cubeCTMS is a comprehensive clinical-trial management system designed to provide end-to-end oversight of trials, from site and investigator tracking, enrollment management and visit scheduling through budget and contract workflows, milestone reporting and document control. It centralizes study operations and automates key processes so sponsors, CROs and study teams can monitor progress in real time, manage tasks across multiple studies, improve site communications and mitigate risk. With built-in dashboards, alerts and audit-ready logging, cubeCTMS supports regulatory compliance (including FDA 21 CFR Part 11 readiness) and enables stakeholders to manage trial timelines, resources and performance from one platform. The system integrates with other CRScube modules (such as EDC, eTMF, pharmacy/RTSM) to provide a unified ecosystem that reduces duplication, improves data flow and supports adaptive workflows during amendments or global roll-outs. -
48
Zendo Lims
SLCLAB
Laboratory information Information Management Software provided by SLCLAB, is a cloud-based software which allows laboratories to have a complete control of the analytical and administrative parts. Compatible with any browser and any device. Totally customizable, configurable, multi-lab and upgradable in users and versions, adapting to the needs of the moment. Connection to all analyzers, integrations with HIS, ERP, CRM, document repository, public or private systems from Government, online results options, batches... etc. Top-quality software at a very affordable price for any laboratory size. Lots of different modules to carry out an exhaustive control and absolute traceability of everything. -
49
LabCloud
LabCloud
LabCloud™ is dramatically changing the world of lab informatics. Integration is fundamental to a successful operation and effective research. LabCloud™ provides a fully integrated platform that allows R&D organizations to better manage research pipelines. Drive innovation while reducing operational expenditures, increasing laboratory compliance, and improving transparency. LabCloud’s Lab Notebook provides scientists with state-of-the-art tools in order to manage all of your information in one place. Full inventory management, item & instrument management, linked to Lab Notebook. Access to dozens of vendors, links directly to inventory, process orders and invoices, plus export to your accounting system. Access your data in a safe and compliant environment. LabCloud's unique software platform allows unparalleled control over data traditionally residing in isolated data silos. Having precise data control enables informed decision-making while ensuring compliance with industry standards.Starting Price: $7,500 per year -
50
Simulations Plus
Simulations Plus
Our reputation as thought leaders in the areas of ADMET property prediction, physiologically-based pharmacokinetics (PBPK) modeling, pharmacometrics, and quantitative systems pharmacology/toxicology is earned through the success our clients have found through their relationship with us. We have the talent and 20+ years of experience to translate science into user-friendly software and provide expert consulting supporting drug discovery, clinical development research, and regulatory submissions.
