Alternatives to adWATCH
Compare adWATCH alternatives for your business or organization using the curated list below. SourceForge ranks the best alternatives to adWATCH in 2026. Compare features, ratings, user reviews, pricing, and more from adWATCH competitors and alternatives in order to make an informed decision for your business.
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ComplianceQuest
ComplianceQuest
Fastest growing Enterprise Quality, Health and Safety Management System (QHSE) natively built and run on the Salesforce platform. Unified QHSE solutions, which combine EQMS and EHS, help our customers of all sizes deliver quality products and services in the safest, most sustainable way by mitigating risk, problems, and inefficiencies while protecting customers, employees, suppliers and brand. Every organization – irrespective of its industry, geography or size – involves an interaction of activities and processes with the environment. These activities may have an adverse or favorable impact on the environment depending on the type of activity being carried out. Our Environment Management solution has been designed to minimize and mitigate these adverse impacts on environment, to such an extent that our already depleting biodiversity is protected, and nurture an ecosystem where all living organisms coexist sustainably.Starting Price: $30 per user per month -
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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. -
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Ennov's Pharmacovigilance Suite is an end-to-end solution for collecting, managing, assessing, and reporting human and veterinary adverse events within a unified database. The suite offers advanced signal detection and data analysis tools, ensuring compliance with global regulatory requirements. Key features include efficient case intake and triage with optimized user interfaces for data entry, flexible case input forms, and searchable vocabulary lists. The system supports both paper and electronic reporting formats, including CIOMS, MedWatch 3500s, and ICH E2B standards (R2 and R3 formats). For signal detection and management, it provides comprehensive data querying, powerful analysis capabilities, and the calculation of key statistical measures such as PRR, ROR, and MGPS. The platform is 100% web-based, user-friendly, and designed to comply with 21 CFR Part 11, ensuring data integrity and security.
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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. -
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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. -
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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 -
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Veeva Vault Safety
Veeva
Veeva Vault Safety is a modern individual case safety report management system that supports the intake, processing, and submission of adverse events for clinical and post-marketed products. Within one system, sponsors and CROs can process global and domestic adverse events for drugs, biologics, vaccines, devices, and combination products. Built-in gateway connections and reporting rules streamline the submission management of cases to health authorities and distribution to partners. Central coding dictionary management automates semi-annual MedDRA, WHODrug, and EDQM updates. Vault Safety unifies pharmacovigilance systems and processes on a single cloud platform to deliver proactive patient safety. It leverages real-time reports and dashboards and seamless collaboration to provide visibility and compliance for adverse events. -
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Kanteron
Kanteron Systems
Kanteron Platform ingested medical images, digital pathology slides, genomics sequences, and patient data from modalities, scanners, sequencers and databases, and provided a complete data toolkit to every team in hospital networks. Pharmacogenomics for adverse medication event prevention, and Precision Medicine application at the point of care: Incorporates sources of drug-gene interaction data that were previously only available in in accessible formats (e.g. tables in a PDF document), implementing the major Pharmacogenomic databases (like PharmGKB, CGI, DGIdb, OpenTargets...) Allows the user to refine their query to certain gene families, types of interactions, classes of drugs, etc. Flexible AI means you can choose the data set that best fits your use case, and apply it to your relevant medical images. -
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Clienvo eTMF
Clinevo
Clinevo electronic Trial Master File (eTMF) is an easy-to-use electronic Trial Master File in electronic (digital content) format for organizing and storing documents, images, and other digital content of clinical trials. Clinevo electronic Trial Master File (eTMF) has an inbuilt DIA reference model and meets regulatory guidelines. Clinevo MICC Intake is a web-based tool for Medical Information Call Center (MICC) and PV users to Log, Track and Monitor Product Quality Complaints (PQCs), Medical inquiries (MIs) and Adverse Events (AEs). Clinevo Safety is a cloud-based, user-friendly, easy-to-use, regulatory-compliant end-to-end Pharmacovigilance / Drug safety system. The All-in-one system provides PV Intake, Case Processing, Regulatory Submissions / AS2 Gateway, Analytics, and Safety signals capabilities under one platform. Clinevo Website Intake is a web-based tool which can be connected to Sponsor / CRO websites to provide Consumers and Reporters a User friendly web interface. -
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Cloudbyz Safety & Pharmacovigilance Solution is a cloud-based software solution designed to streamline the drug safety and pharmacovigilance operations for pharmaceutical and life science companies. The solution helps to automate the process of collecting, processing, analyzing and reporting adverse event data in compliance with global regulatory requirements. Cloudbyz Safety & Pharmacovigilance Solution enables companies to reduce risk, improve compliance, and enhance patient safety while accelerating drug development. 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.
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ExtraView
ExtraView
ExtraView is an enterprise software platform implementing business process management, global quality management systems for CAPA, adverse event reporting, food safety, bug and defect tracking, change management, customer support, helpdesk, field audit, and other workflow or issue management systems. Use out-of-the-box solutions or implement a custom requirement. Available as a service in the cloud or on your own servers. Simple to configure, yet provides a quality platform on which to implement fully validated systems such as incident management, CAPA, adverse event reporting, & root cause analysis, clinical trial data management and food safety. Implement bug-tracking, customer support, requirements management, change management and other issue-tracking systems. Many customers can take advantage of the full-featured, free, downloadable version! Learn how financial companies implement systems that regulate and control audit systems, provide corporate governance and risk management.Starting Price: $400 one-time payment -
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CoVigilAI
CoVigilAI
CoVigilAI is an AI-enabled medical literature monitoring solution that employs advanced algorithms and data analytics to proactively detect and manage adverse drug events, ensuring patient safety and regulatory compliance in real time. The platform offers streamlined tracking of scientific and medical publications across prominent global literature databases such as PubMed and Embase, with customizable search strings facilitating an effortless pharmacovigilance literature monitoring journey. Periodic surveillance of scientific and medical literature databases and publications from diverse local journals is conducted, encompassing both global literature monitoring and localized literature surveillance. Advanced algorithms categorize Individual Case Safety Reports (ICSRs) into valid, potential, and invalid cases, while automated key entity detection efficiently recognizes crucial entities like patients, medications, adverse events, and designated medical events. -
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MediGrid
MediGrid
MediGrid has a smart data ingestion engine that not only structures your data well and helps to curate your data, it is also able to transform and harmonize your data. This allows researchers to conduct multi-study analyses or to review adverse effects across multiple studies for example. During various phases of your research you want a realtime view of the safety of all patients. Especially when it comes to monitoring of adverse effects (AE) and serious adverse events (SAE) before or after market introduction. MediGrid can help you monitor, detect and warn you about these safety risks. This will improve patient safety and prevent you from getting a bad reputation. MediGrid also does the heavy lifting in terms of collecting, classifying, harmonizing and reporting the safety data. -
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mydimed
mydimed
Preventive medicine is the future of medicine. We help healthcare providers identify and intervene with high risk patients. Helping clinicians keep patients safe. Lowering ADR inside Healthcare providers facility Between 5%-10% of hospitalized patients have an ADR during their hospitalization, an adverse event that increases risk, increases length of stay, and denies reimbursement from payers for additional hospitalization days and procedures. These Adverse Drug Reactions can be prevented. Helping ACO's, HMO's and payers to reduce preventable ER visits and hospitalization. Lowering ADR among the population with emphasis on the Elderly. Between 15%-30% of all 65+ years old patients ER visits are due to an ADR. These visits are often accompanied by hospitalization. These Adverse Drug Reactions are preventable. What We Do. Advanced Science Multi disciplinary science. Our technology is based on medical research and advanced data science, a powerful combination that yields better -
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Mesh Bio
Mesh Bio
Based on proven medical science and explainable systems biology, DARA enables and enhances clinical decision support and intervention guidance. We work with healthcare providers and stakeholders to provide digital solutions that transform health screening and chronic disease management. We enable digital transformation of care delivery through clinical workflow automation and predictive analytics, built on gold standard clinical guidelines and best practices. We help physicians engage with patients better by providing actionable health insights through personalized disease risk and adverse event predictions. We guide pharmaceutical development by revealing pharmacodynamics in complex biological processes and find novel therapeutic interventions. Predictive analytics on multidimensional patient data will enable personalized precision medicine in the management of cardiometabolic disease to prevent catastrophic patient outcomes. -
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GoResearch
2KMM
GoResearch™ is a fully validated, innovative internet platform for electronic data capture(EDC) created by 2KMM for research projects such as clinical/observational studies andpatients registries. It offers a wide range of features supporting such projects invarious areas such as: configuration of the information flow and the Adverse Events management procedures (including automatic e-mail notifications to safety departments), random allocation to a treatment arm through the built-in randomization module, data collection with the use of individually customized case report forms (eCRF) to meet the requirements of each study, and ePRO, eSource and mHealth data integration through dedicated mobile and/or web applications or flexible application programming interface (API). -
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IQE is MediaLab’s non-conforming event management system that allows clinical laboratory teams to track, assess, and prevent non-conforming events (NCE). With the capability to import or create event forms and data logs, IQE enables laboratory teams to eliminate deficiencies, correct common NCEs, and, most importantly, focus on improving healthcare. With a MediaLab institutional subscription, administrators can easily document each phase of the event management lifecycle, from initial event description to risk analysis, investigation, and root cause analysis, corrective and preventive actions plans, and overall CAPA effectiveness evaluations. IQE supports: • Customizable, pre-built event forms and workflow • Monitoring and evaluating change control events, failed PT events, customer complaints / feedback, safety / injury events, supplier / vendor issues, and more • Tracking periodic data entries • Robust reporting and dashboards to identify common NCEs and CAPA effectiveness
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ClinSoft
Innovate Research
Innovate’s End-To-End Clinical Data Management Services. Our clinical data management processes, expertise and technology are developed to make each step of your clinical trial data management process more accurate and efficient for Phase I-IV in wide range of therapeutic areas. Our CDM Team Is Well-Versed With Current Good Clinical Data Management Practices (cGCDMP) International conference on harmonization Good Clinical Practices (ICH-GCP) 21 CFR Part 11 Compliance Health Insurance Portability and Accountability Act (HIPAA) Requirements Applicable Regulatory Guidelines SAS datasets SAS XPORT transport files EDC Helpdesk Support 24/7 On-Site and Off-Site Clinical Data Management Services Electronic Data integration and transfer Quality Control Activities Medical Dictionary for Regulatory Activities (MedDRA) Serious Adverse Event (SAE) Reconciliation Clinical Database Transfers Clinical Database Lock paper Case Report Form (pCRF) and electronic Case Report Form. -
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VigiLanz Vaccinate
VigiLanz
VigiLanz Vaccinate provides end-to-end management of your entire vaccination process – supporting mass vaccination events while managing organizational COVID-19 risk. Enable healthcare workers to easily register and provide consent. Eliminate manual data entry and automate workflows for program administrators. Reduce vaccine waste with real-time insights into volume needs based on scheduling and demand. Gain real-time visibility into vaccination and immunity rates at the individual, department, hospital, and enterprise-level. Automate data collection for CDC and state reporting, including for adverse side effects. Pre-register vaccine candidates, assess workforce readiness, centralize immunity factors from outside the organization, collect adverse responses and manage consent forms. Quickly move healthcare workers through the vaccination process using efficient forms. Manage automated reminders to register for secondary doses and to report adverse events. -
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The Multum drug, herbal, and nutraceutical database is a leading industry resource designed to assist you in your safe medication use efforts and prevention of adverse drug events. The software solutions and databases created by Multum provide pertinent drug information and are designed to help your clinicians safely recommend medications with the accurate dosage while addressing drug interaction concerns. Lexicon Plus provides a foundational database with comprehensive drug product and disease nomenclature information to link with our clinical information systems and other outside systems. VantageRx Database contains drug knowledge in a Microsoft Access format that embeds into your own application and delivers essential clinical content through a series of database tables. Organizations receive development interfaces. We help ensure your needs are met by enabling third-party applications to integrate specialized features into our software through an open and secure platform.
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dezzai Sentria
dezzai
Sentria is an artificial intelligence-powered platform designed for adverse event case management and post-marketing surveillance. It offers an intuitive, customizable, automated, and industry-compliant software solution to enhance the capacity, speed, and precision of adverse event management. The platform facilitates pharmacovigilance compliance with ICH international regulatory guidelines and ensures the proper evaluation of adverse events following local regulations. Sentria streamlines capturing reports through an intuitive interface enhanced by pharmacovigilance automation, reduces capture errors through intelligent alerts, and facilitates report processing using international MedDRA, and ATC/WHO coding. It increases analytical capabilities using semantic artificial intelligence for pharmacovigilance. The platform includes features such as secure access controlled with credentials, auditable logs for compliance, and an encrypted cloud environment. -
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Salesforce Agentforce Life Sciences
Salesforce
Agentforce Life Sciences, formerly Life Sciences Cloud, is Salesforce’s AI-first engagement platform built for Pharma, MedTech, Consumer Health, and Animal Health organizations. It unifies clinical, medical, commercial, and patient services functions on a compliant, industry-specific CRM foundation. The platform enables cross-functional teams to engage healthcare providers and patients using real-time, data-driven insights. AI-powered automation accelerates clinical trials, improves medical inquiry management, and enhances commercial engagement. Life Sciences Cloud supports compliant workflows with audit trails and governance embedded directly into daily operations. Patient services teams can streamline benefits verification, adherence programs, and adverse event management. Agentforce Life Sciences helps organizations bring therapies and devices to market faster while improving operational efficiency and stakeholder engagement. -
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ClinionAI Medical Coding
Clinion
Fully automated AI-enabled, Medical Coding software to help your team work faster and smarter. ClinionAI uses Deep Learning NLP models to automate the coding of Adverse Events and Concomitant Medication. The AI Medical Coding algorithm has been trained on millions of biomedical terms for medical context learning using machine learning models. MedDRA dictionaries are encoded and embedded in the model. Adverse event terms entered into Clinion EDC are matched with the MedDRA dictionary terms by the ML Algorithm and results with associated confidence scores are displayed. Users can choose the best fit! -
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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. -
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TrominoCARE
TrominoSoft
TrominoCARE is a scalable, cloud-based Medical Information Call Center (MICC) software designed to automate daily operations within medical information call centers. It features a comprehensive database that supports the entire lifecycle management of MICC activities, handling various call types such as medical inquiries, product quality complaints, and adverse events. Accessible via mobile phones, tablets, and desktops, TrominoCARE ensures flexibility and responsiveness across devices. Key capabilities include process automation for managing all call types, automatic generation of Field Alert Reports (FARs), a configurable client product dictionary, and customizable workflows tailored to specific business needs. The platform also offers a mobile application enabling medical sales representatives and field teams to capture and report information offline, with integration capabilities for safety and MICC systems. -
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LifeSphere Medical Affairs
ArisGlobal
LifeSphere Medical Affairs is a cloud-based platform developed by ArisGlobal to enhance efficiency, compliance, and collaboration within medical affairs teams. It offers a unified workspace that seamlessly integrates medical information management with safety and quality systems, enabling end-to-end automation and real-time data sharing. The platform streamlines the intake and management of medical inquiries across multiple channels, automates the processing of product complaints and adverse events, and ensures consistent global compliance with evolving regulatory requirements. Its advanced analytics and reporting tools provide actionable insights, facilitating data-driven decision-making and improved patient outcomes. LifeSphere Medical Affairs is designed to be scalable and configurable, catering to the unique needs of organizations of all sizes. -
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TheraDoc
DSS
TheraDoc® provides a real-time picture of the raw data within a hospital’s source systems, helps alert clinicians to potential risks and empowers them with knowledge to improve clinical outcomes, lower costs and strengthen regulatory compliance. Quickly adapt to changes in regulatory and reporting, guideline updates, and the evolution of surveillance scale and scope. Streamline workflows tailored to VA clinical programs. Reduce adverse events and clinical errors. TheraDoc enabled case review, correct isolation, changes to cleaning practices, and more appropriate lab testing. The Antimicrobial Stewardship Program that includes Clinical Pharmacists working daily with providers was a strong driver for change. -
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NewTn-SAFETY
NewTn-SAFETY
NewTn's SAFETY is an advanced pharmacovigilance cloud platform designed to accelerate safety processes and simplify compliance for pharmaceutical companies, startups, and contract research organizations. The system offers a comprehensive suite of features, including cloud-based scalability for superior data storage and processing capabilities, data reusability to eliminate redundant entries, real-time alerts and monitoring for prompt adverse reaction detection, and robust reporting functions that facilitate the generation of DSUR and PBRER reports. Tailored use cases highlight its benefits in establishing pharmaceutical safety databases for startups, providing cost-effective safety systems for budget-sensitive CROs, enhancing regulatory compliance for small and medium-sized pharmaceutical companies, and delivering comprehensive safety data analysis and reporting. The platform's intuitive UI/UX and support for DSUR/PBRER reporting make it a customized solution. -
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Artrya
Artrya
Artrya partners with clinics receiving chest pain patients to deliver new models of cardiovascular care based on AI. Easily integrate plaque features of high prognostic value into the evaluation of coronary artery disease. Rapid assessment of chest pain patients in emergency and primary care settings. We see a world where communities do not have to be plagued by a high rate of a heart attack. AI-driven insights into the type and volume of arterial plaque detected through coronary computed tomography angiography (CCTA) facilitate the accurate stratification of chest pain patients within minutes. Quickly determine patients with minimal to zero coronary artery disease with the confidence there are no underlying plaque features that could cause future major adverse cardiac events. Catch the early warning signs of a potential heart attack. Effectively rule in at-risk patients with acute or atypical chest pain who warrant further investigation and therapy. -
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Merlon
Merlon
The world’s most advanced AI-powered adverse media research platform for enhanced AML and KYC Investigations. Merlon’s advanced natural language processing engine extracts and categorizes risk topics to ensure relevance to both FATF guidelines and financial institution controls. Key biographical information is extracted to effectively match against client details. Articles are clustered into unique events, thereby minimizing the number of articles that must be read. Duplicates are intelligently identified and filtered out, significantly cutting investigation time. Results are sorted by AML risk relevancy, ensuring analysts uncover risk sooner. Our natural language processing algorithms identify risk beyond the reach of traditional solutions. Irrelevant articles are suppressed from results, ensuring analysts do not waste time on non-material articles. -
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SmartSig
DrFirst
An estimated 66% of data from the nation’s largest medication history database is missing essential sig information. That can leave your patients at significant risk of an adverse drug event or worse. It doesn’t have to be that way. SmartSigSM from DrFirst fills the information gaps left from missing sig data quickly, efficiently and accurately. Building on robust predictive data delivered by SmartStrings, which automatically identifies the most commonly prescribed medications, SmartSig intelligently translates free text data, even safely inferring missing components, using statistics and clinical analytics to produce a real-time translation in a click. This essential interoperability tool takes less than two hours to implement and is compatible with major electronic records giving you more time to spend with your patients and a proven way to improve patient safety. -
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QAPI360
QAPI360
QAPI360 is a cloud-based, HIPAA-compliant Quality Assurance Performance Improvement (QAPI) software that centralizes, organizes and tracks all elements of a healthcare provider’s quality program so agencies can move beyond spreadsheets and disconnected processes to a systematic, data-driven approach; it includes structured QAPI plans, quality indicators, patient and staff incident tracking, infection control surveillance, medication error and adverse drug reaction logs, hand hygiene programs, performance improvement project templates, patient satisfaction surveys, and contracted provider performance tracking, with interactive dashboards, trending and analysis that help users visualize patterns, implement corrective actions, and monitor outcomes; it supports easy data entry, EMR integration or automated imports, built-in reporting and charts for compliance documentation and audits, and tools to streamline data collection, charting, and root-cause analysis.Starting Price: $249.99 per month -
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SAMS
Solytics Partners
SAMS™ is the next-generation, integrated Screening Solution for all Sanctions, PEP, and Adverse Media Screening needs. Our proprietary database comprises 600+ global/regional Sanctions and Watchlists, 5 million+ PEP entries, and Adverse Media from 55,000+ sources in 50+ languages, updated in near real-time. It also has the flexibility to add other 3rd party or internal databases. SAMS™ is powered by intuitive workflows designed by leading industry experts and automates initial customer screening and ongoing monitoring processes. It has been designed with robust checks and controls, a complete audit trail for regulatory reporting, and powerful visualization capabilities to aid decision-making.Starting Price: $500/month/user -
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InSilicoTrials
InSilicoTrials
InSilicoTrials.com is a web-based platform, which provides a user-friendly computational modeling and simulation environment where many integrated easy-to-use in silico tools are readily available. The platform targets primarily users from the medical devices and pharmaceutical sectors. The in silico tools available for medical devices enable computational testing in different biomedical areas like radiology, orthopedics and cardiovascular during product design, development and validation processes. For the pharmaceutical sector, the platform provides access to in silico tools developed at all stages of the drug discovery and development processes and for many different therapeutic areas. We have built the only cloud-platform based on the crowdscience concept that makes it easy to use validated models and cut your R&D costs now. A growing catalogue of models ready to be used, on a pay per use basis. -
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Grand Avenue Software
Grand Avenue Software
A web-based quality system software suite that helps medical device companies automate their processes and simplify regulatory compliance. Modules include: Audit Management, CAPA, Complaint Handling, Design Control, Document Control, Equipment Management, Nonconforming Materials Reporting, Supplier Management and Training Management. Designed from the beginning for ISO 13485 and 21 CFR Part 11 compliance. Audit results are recorded for each requirement in the audit. Requirements are marked as conforming, nonconforming, or not applicable. Each result may be detailed with one or more findings. Findings that may be recorded include observations, major nonconformances, and/or minor nonconformances. Findings may result in Corrective and Preventive Actions (CAPA) and/or may be documents with audit actions already completed. -
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SafetyEasy
AB Cube
Efficient drug safety operations with the technological expertise of industry veterans begins here. Align international pharmacovigilance operations teams with an intuitive, unified, cloud-based safety system trusted by industry leaders. SafetyEasy® Suite is a multivigilance management solution which integrates automation with existing drug safety processes. Growing biotechnology firms trust individual vigilances provided by AB Cube for their safety regulatory processes. Life sciences organisations manage adverse event reporting and stay compliant with the latest regulations with SafetyEasy® Suite. SafetyEasy® Suite is AB Cube’s all-in-one ecosystem for automated multivigilance management. Built to make safety simple, scalable, and smart. Designed for organizations of all sizes, it’s a modular, cloud-based platform that automates every step of the vigilance process, from early stage data capture to regulatory reporting and advanced analytics. Flexible and compliant by design, -
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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. -
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Ripjar
Ripjar
Ripjar is an AI-driven risk and compliance intelligence platform that helps enterprises, financial institutions, governments, and security teams detect, monitor, and investigate threats and risks across people, entities, and data at scale. Its products combine advanced machine learning, natural language processing, and entity resolution to integrate and analyze structured and unstructured data, including sanctions lists, watchlists, adverse media, internal records, transactions, and third-party sources, to produce dynamic risk profiles that update in real time and significantly reduce false positives and false negatives compared with traditional screening systems. Ripjar’s solutions include AML name screening & monitoring that consolidates disparate compliance outputs into a unified view; adverse media screening to surface reputational and hidden risk signals; and third-party risk management to continuously assess compliance, ethical, prudential, and supply-chain risks. -
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Milsoft FMS
Milsoft Utility Solutions
You already have a myriad of decisions to make. Decisions that affect the allocation of resources to manage your utility effectively. Having either inaccurate or late information can have adverse effects on your choices. Our FMS is designed especially for utilities to support workflows tailored to our market space. The tools available to your accounts team makes FMS an invaluable aid in getting the financials exactly where they need to be. In a system built to take the data, put it into the correct accounts, and to generate the reports required by stakeholders. -
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Over the last several years, the Life Sciences industry has faced nearly $15 billion in fines and compliance-related settlements, making it critical for companies to adhere to pharmaceutical, medical device and biotech best practices. Efficient and effective management of clinical trials can also significantly impact the time, scope and budget for the development of a drug or medical device. With OpenText™ Clinical Trial Quality Management System (ctQMS), companies can remain compliant, reduce costs of records management and establish best practice through collaboration before, during and after the clinical trial lifecycle.
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Genomenon
Genomenon
Pharma companies need comprehensive genomic information to drive successful precision medicine programs, but decisions are often made using only a fraction of the data available, about 10%. Genomenon delivers 100% of the data. An efficient and cost-effective natural history research solution for pharma, ProdigyTM Patient Landscapes support the development of rare disease therapies by enhancing insights contained in retrospective and prospective health data. Using a powerful AI-driven approach, Genomenon delivers a comprehensive and expert assessment of every patient in the published medical literature, in a fraction of the time. Don’t miss anything, get insight into every genomic biomarker published in the medical literature. Every scientific assertion is supported by empirical evidence from the medical literature. Identify all genetic drivers and pinpoint which variants are known to be pathogenic according to ACMG clinical standards. -
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SimpleTrials
SimpleTrials
SimpleTrials is an on-demand, subscription-based Clinical Trial Management System (CTMS) designed for sponsors, Contract Research Organizations (CROs), and investigative sites. It offers a comprehensive suite of tools to effectively plan, manage, and track clinical study portfolios, including features such as site startup and subject tracking, document management with integrated electronic Trial Master File (eTMF), real-time study analytics, calendar and monitoring, custom fields and trackers, ad-hoc reporting, planning and milestones, site contracts and payments, and electronic visit reports. It supports compliance with 21 CFR Part 11 and provides a secure, validated environment for clinical trial data. Users can customize tracking views, integrate with various Electronic Data Capture (EDC) systems, and utilize built-in templates for consistent document management.Starting Price: $849 per month -
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Medidata
Dassault Systèmes
The Medidata Clinical Cloud is our cutting-edge platform that transforms the clinical trial experience for patients, sponsors, CROs, and research sites. As the only unified technology platform dedicated to clinical research, the Medidata clinical cloud addresses the holistic research process from start to finish. Our platform helps life science and medical device organizations cut development costs, mitigate risks, and deliver treatments and devices to market faster. No matter which products you choose for your clinical trial program, you will have access to the power of the Medidata Clinical Cloud. At Medidata, we’re leading the digital transformation of clinical research. Powered by artificial intelligence, machine learning and advanced analytics, our platform brings researchers, study managers, investigators, and patients together to accelerate research. Obtain regulatory-compliant, patient-friendly electronic informed consent for clinical trials. -
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Folio3 Clinical Trial Management
Folio3 Digital Health
Folio3 Digital Health's Clinical Trial Management Software (CTMS) is a comprehensive, web-based platform designed to streamline the entire clinical trial lifecycle for pharmaceutical companies, CROs, and research organizations. It centralizes trial operations, from planning and site management to data collection and reporting, ensuring compliance with global regulations like FDA 21 CFR Part 11, GxP, and HIPAA. The software emphasizes user-friendly interfaces, real-time dashboards, and scalable modules to handle trials of any size efficiently. Core Modules The platform features dedicated modules for study setup, where users define protocols, timelines, and budgets with customizable templates. Site management tools track investigator qualifications, contracts, and payments, while patient recruitment capabilities include screening, enrollment tracking, and visit scheduling with automated reminders.Starting Price: $300 -
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CAPA Manager
Adaptive Business Management Systems
Automate the identification, containment, investigation, and resolution of problems within your organization and supply chain. Trusted by thousands of users globally, this is one of the best CAPA software applications available. CAPA Manager corrective action software automates the assignment, notification, investigation, reporting, and approval of corrective actions. It error-proofs the control of the entire CAPA process, from initiation to investigation and all the way through to closure. CAPA Manager meets the requirements of all important quality management standards: 21 CFR part 11, ISO 9001, AS9100, TS 16949, and more. It keeps records of root-cause and corrective action while providing pre-defined workflows and approval gates.Starting Price: $12.49 per user/month -
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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. -
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Tepsivo
Tepsivo
Tepsivo's pharmacovigilance software solutions are designed to streamline drug safety processes through automation and smart templates, significantly reducing administrative burdens and associated costs. The Tepsivo Platform is a comprehensive, cloud-based application that allows users to manage all pharmacovigilance activities in one centralized location. Key features include a Quality Management System, Local Contact Person for Pharmacovigilance (LCPPV) oversight, streamlined safety reporting and follow-up tools, PSUR tracking, signal management tracking, automated audit trails, compliance tracking, adverse event intake tools, literature monitoring, risk management system tracking, PSMF management solutions, automated partner reconciliation, and CAPA management. These integrated modules ensure full transparency, 100% compliance, inspection readiness, high quality, rapid speed, no administrative overhead, and minimal cost. -
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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. -
49
BEKhealth
BEKhealth
BEKhealth offers an AI-powered clinical research platform centered on its BEKplatform, a unified system that extracts, interprets, and standardizes structured and unstructured electronic medical record data, including labs, diagnoses, physician notes, pathology reports, and PDFs, into a searchable, longitudinal patient graph to help life sciences and healthcare organizations rapidly identify protocol-eligible patients and optimize trial feasibility, site selection, and recruitment workflows. It employs deep learning and natural language processing to transform disorganized clinical data into actionable insights with high accuracy, generating robust queries and patient cohorts that reveal more qualified candidates than traditional manual chart review and support feasibility analyses with real-time reports and dashboards that inform decisions across research networks. -
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Citeline
Citeline
Citeline is a clinical development intelligence and analytics platform that provides real-time R&D data, insights, and tools to life sciences organizations to inform strategic decisions across the drug and device development life cycle. It aggregates and curates the world’s most extensive datasets on global clinical trials, investigators, trial sites, drug development pipelines, and regulatory requirements, supporting functions such as protocol design, feasibility analysis, site and investigator selection, enrollment forecasting, competitive benchmarking, and compliance tracking with disclosure obligations across jurisdictions. It includes products like Pharmaprojects for pipeline monitoring, Trialtrove for clinical trial benchmarking, Sitetrove for site/investigator intelligence, Global Patient Insights for aligning feasibility with real patient access, and TrialScope Intelligence/Disclose for managing regulatory disclosure requirements.
