Alternatives to PharmaPendium
Compare PharmaPendium alternatives for your business or organization using the curated list below. SourceForge ranks the best alternatives to PharmaPendium in 2025. Compare features, ratings, user reviews, pricing, and more from PharmaPendium competitors and alternatives in order to make an informed decision for your business.
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IQVIA
IQVIA
Thousands of organizations around the world trust IQVIA to speed drug development, ensure product quality and safety, improve commercial effectiveness, get the right treatments to patients, improve access to and delivery of healthcare, and ultimately drive better health outcomes. Reimagine clinical development by intelligently connecting data, technology, and analytics to optimize your trials. The result? Faster decision making and reduced risk so you can deliver life-changing therapies faster. With a foundation in data, advanced analytics, and expert insight, IQVIA brings specialized capabilities to customers across the healthcare ecosystem. Read and watch the latest from IQVIA data scientists, doctors, researchers, and other subject matter experts on the topics that matter to you. From industry trends to how we are applying our capabilities to help, you can find it here. -
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Embase
Elsevier
Improve your biomedical research with the world’s most comprehensive biomedical literature database. More biomedical evidence by searching comprehensive, relevant, and up-to-date biomedical research. Create systematic searches and automate query building using intuitive search forms. Uncover drug-disease relationships and drug-drug interactions, manually curated from deep indexing. The accelerated pace of biomedical research and development demands comprehensive information. You anticipate risk by assessing everything that is known. You track safety to meet regulations. You uncover connections to push innovations. Embase is a unique medical literature database where comprehensive goes beyond content. With Emtree indexing of full-text content and dedicated search terms, you find all relevant and current results. This includes information that may not be uncovered in other databases. Scroll down to find out why regulatory agencies recommend Embase in their best practice guidelines. -
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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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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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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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Oracle Life Sciences Empirica is the market-leading solution for detecting, analyzing, and managing safety signals originating in pre- and post-market drugs, biologics, vaccines, devices, and combination products. Oracle continually researches, develops, and advances the state-of-the-art data-mining algorithms and statistical techniques used in Empirica. By enabling the detection of signals with a longer lead time, Empirica can provide risk insights 7 to 22 months earlier than labeling revision dates from a time-indexed benchmark. Safety teams responsible for signal management face new challenges, such as finding hidden signals, assessing information from multiple big data sets, and providing better safety information before clinical trials even begin. Read our ebook to learn how new advances in methodologies and technologies, such as artificial intelligence, can help address these challenges.
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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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DF mSafety AI
Datafoundry
DF mSafety AI is a cloud-based safety platform that leverages AI/ML and automation to enhance efficiency and user experience in safety case management and signal detection for drugs, cosmetics, vaccines, nutraceuticals, and medical devices. Built on Datafoundry's loud platform, DF Safety 4.0, it supports scalable and secure AI/ML-driven safety case and signal management, with pre-built connectors to enterprise systems, adhering to regulatory requirements and industry standards. Key features include multi-source case intake options, automated triage rule configuration, seriousness prediction, causality assessment, expectedness and listedness assessment, auto narrative generation, custom report generation, literature monitoring for safety, signal and risk management, case compliance alerts, integrated MedDRA and WHO-DD browsers, enhanced E2B R2 & R3 compliance, and an e-submissions gateway. -
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PubHive Navigator
PubHive
PubHive Navigator is an AI-powered software platform that streamlines scientific literature and safety workflows for life science companies of all sizes. It offers centralized end-to-end workflow solutions for literature review, curation, annotation, collaboration, searching, reporting, citing, and managing research. The platform features AI-powered smart workspaces for centralized literature management, collaborative research writing and team communication, reuse rights and document delivery integrations, and out-of-the-box workflows for different operation units. PubHive Navigator is designed to simplify enterprise scientific literature and safety information workflows, making it a flexible software platform for teams in drug safety and pharmacovigilance, medical affairs, clinical affairs, and R&D. -
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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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DF mSignal AI
Datafoundry
DF mSignal AI is a modular, scalable, and secure safety signal management system designed to enhance the efficiency of signal detection and risk management processes across pharmaceuticals, vaccines, medical devices, cosmetics, and nutraceuticals. The platform offers active and passive surveillance with real-time monitoring of product-event combinations, customizable clinical risk flags, and an interactive user interface with advanced analytics. It integrates seamlessly with MedDRA, WHO-DD, clinicaltrial.gov, and electronic data capture systems, providing a comprehensive solution for safety professionals. DF mSignal AI automates the computation of statistical scores, saving time and ensuring accuracy in signal detection and evaluation. The system is designed to meet all applicable regulations and guidance, such as 21 CFR Part 11, data integrity and privacy controls, and GxPs, ensuring compliance and security. -
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Thrana Safety Database
Thrana Softech
Thrana Safety Database, a cloud-based pharmacovigilance and drug safetysystem. Designed with user-friendliness in mind, this end-to-end solution seamlessly integrates key functionalities such as PV Intake, Case Processing,Regulatory Submissions (AS2 Gateways),Regulatory Reports, and Analytics—allaccessible from a centralized platform.Starting Price: $17000 USD/year -
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DrugCard
DrugCard
DrugCard is an AI-enabled data intelligence platform designed to streamline pharmacovigilance processes by automating local literature screening. The platform supports over 100 languages and monitors more than 1,000 local medical journals across 55+ countries, ensuring continuous, regular, and transparent monitoring. By automating routine tasks, DrugCard enables Contract Research Organizations (CROs) to manage more pharmacovigilance projects and improve screening results, Marketing Authorization Holders (MAHs) to conduct in-house literature screening more effectively, and freelancers to save up to 70% of their time for other value-adding activities. The platform is designed to be scalable to new markets, cost-effective, and compliant with regulatory requirements, providing a comprehensive solution for drug safety departments. -
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Drug Safety Triager
Clarivate
Drug Safety Triager is Clarivate's next-generation pharmacovigilance software designed to assist life sciences organizations in meeting regulatory requirements. This GxP-validated, compliant, and audit-ready system manages and streamlines the literature review workflow, enabling pharmacovigilance experts to focus on patient safety by simplifying literature review processes. The platform is fully validated and compliant with the reporting requirements of global safety regulatory agencies such as the FDA and EMA. Each implementation of the Drug Safety Triager is delivered with a validation package. The validation process and associated documentation align with the pharmaceutical industry and health authority regulations. All literature references undergo a systematic review process that automatically captures all users’ actions and adds a permanent, non-editable audit trail to the record. -
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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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Oracle Argus
Oracle
The market-leading, trusted solution for processing, analyzing, and reporting adverse event cases originating in premarket and post-market drugs, biologics, vaccines, devices, and combination products. Transform your case management efficiency with innovative capabilities, such as built-in automation, workflow optimization, and conditional touchless processing. You can depend on Argus, a mature, reliable solution providing proven compliance with drug, vaccine, and device regulations and standards in all regions of the world, including E2B(R3), E2B(R2), eVAERS, eMDR, MIR, and IDMP. Argus Advanced Cloud includes Oracle Analytics, a powerful, flexible, AI-powered solution that empowers users to uncover new insights and make faster, more informed business decisions. Medicinal product safety teams face enormous pressure to control ever-increasing caseloads, new sources of signal detection data, and changing regulations, all with flat budgets and resources. -
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SafetyEasy
EXTEDO
EXTEDO's SafetyEasy is a comprehensive pharmacovigilance and multivigilance management software designed to streamline the processing of safety cases and vigilance data. It ensures compliance with various drug safety regulations, including E2B(R3) and HL7 eMDR, and supports the generation of essential regulatory documentation such as PSUR, PBRER, and DSUR. The platform offers features like workflow optimization through email notifications and online dashboards, enabling users to track project statuses and meet submission deadlines efficiently. SafetyEasy also incorporates advanced modules like CasEasy AI, which utilizes Natural Language Processing to automate case creation and a Business Intelligence module that provides a dynamic 360° view of scientific data to enhance case analysis and safety signal detection. As a cloud-based service, SafetyEasy™ is quick to implement, user-friendly, and requires minimal training. -
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Clinevo Safety
Clinevo Technologies
Clinevo Safety is a cloud-based, user-friendly, regulatory-compliant, end-to-end pharmacovigilance and drug safety system. This all-in-one platform encompasses PV intake, case processing, regulatory submissions via an AS2 gateway, analytics, and safety signal capabilities. Built on a simplified technology stack, it offers extensive configurations with minimal customizations, resulting in lower total cost of ownership and easy maintenance. The system provides end-user alerts for cases nearing due dates, ensuring timely compliance. Advanced automation and AI features streamline case processing efforts, while easily configurable dynamic workflows expedite case management. The platform delivers powerful and actionable insights through advanced analytics. As a user-friendly web application, it is accessible anytime, anywhere, and on any device with basic internet or intranet using browsers like IE, Chrome, and Firefox. -
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AccelSafety
Techsol Life Sciences
AccelSafety is a comprehensive pharmacovigilance platform developed by Techsol Life Sciences, built around the Oracle Argus Safety application to address the unified collection, medical assessment, and regulatory reporting of clinical and post-marketing safety surveillance data. The fully managed cloud solution facilitates emerging biopharma companies, device manufacturers, and service providers in managing safety data and making informed business decisions in alignment with global compliance requirements. Key benefits include fast-track Argus Safety implementation, migration, and validation with a 70% effort reduction; secure migration of legacy safety data to the AccelSafety Cloud; simplified lean case processing through customized configurations and native automation; comprehensive operational insights via advanced reports, line listings, and analytics packages; and 24/7 Argus Safety Service Desk support for user requests, incidents, and change management. -
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PvEdge
PvEdge
PvEdge is a cloud-ready pharmacovigilance software designed to provide end-to-end compliant safety solutions for drugs, devices, vaccines, and combination products. It offers a comprehensive safety database that manages pharmacovigilance intake, case processing, submissions, AI & analytics, and safety signals all in one platform. The system adheres to existing and upcoming regulations, such as 21 CFR Part 11, ANNEX 11, GxP, and GDPR, ensuring global compliance. PvEdge utilizes advanced automation powered by AI and machine learning algorithms to enhance efficiency in drug safety database management. Key features include automated literature monitoring, ICSR submissions, smart triage, automated signal detection, and document automation. The platform also provides a controlled document management system for creating, managing, and publishing pharmacovigilance documents, as well as a risk-based enterprise quality management system to implement quality processes and training records. -
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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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TARA PV
MedGenesis
TARA PV is a comprehensive, web-based pharmacovigilance safety database designed for processing, storing, analyzing, and reporting adverse events related to drugs, devices, and vaccines. Developed by MedGenesis Ltd, an ISO 9001 and ISO 27001 accredited UK-based software development company, TARA PV offers a user-friendly interface that is simple, intuitive, and fully compliant with 21 CFR Part 11, GxP, ICH standards, and global pharmacovigilance data protection regulations. As a cloud-based solution, TARA PV requires no installation and is accessible via an internet browser, enabling rapid implementation and integrated workflows for individual case assignments. The system provides full training upon deployment, with ongoing support available through an online ticketing system. Security is a priority, with hosting that features multiple redundancies and triple-layer backups. TARA PV offers a range of transparent pricing models with no hidden costs. -
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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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IQVIA Vigilance Platform
IQVIA
IQVIA Vigilance Platform is an integrated, comprehensive platform built to simplify safety and pharmacovigilance processes while boosting speed, accuracy, and efficiency. Delivered in our secure SaaS environment, using proprietary artificial intelligence, machine learning, and natural language processing algorithms, Vigilance Platform delivers insights that improve compliance, and product safety, and add value to your product development process. The platform covers every aspect of pharmacovigilance processes, capturing cases from patients through case processing, case submission to all authorities, and all case types. An intuitive interface makes IQVIA Vigilance Platform easy to use for affiliates, case processing teams, and signal detection teams. A transformational approach to pharmacovigilance improves compliance so you can focus on delivering safer, more effective drugs and devices faster. -
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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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Fusion eClinical Suite
Axiom Real-Time Metrics
Fusion is Axiom’s proprietary easy-to-use and cost-effective eClinical solution that is focused on small to medium sized device, pharma, and biotech companies. With Axiom’s Fusion eClinical Suite, you can add-on any Modules to meet your study requirements. Running a small study? Just choose the base configuration with EDC, DM and AE/SAE Tracking. Running something more complex? Include powerful Modules such as Inventory Tracking, RTSM, Safety Management to make the management of your study so much easier. Save time by capturing your study data electronically – even when offline! Data syncs to your Fusion databases once an internet connection is established. Access real-time records for Subject screening activities. Safety Database for the management of pharmacovigilance events directly within Fusion. -
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OpenSourcePV
OpenSourcePV
OpenSourcePV is a company founded by Lionel Van Holle in 2019 with the ambition to make use of free & open source technologies to raise the standards of pharmacovigilance and provide an affordable & competitive alternative to expensive software specialized in pharmacovigilance. To meet their regulatory obligations, pharma companies need to monitor the safety of their products. When they start to have a strong pipeline and multiple products on the market, the amount of data to be reviewed is soon too large to be reviewed manually. To benefit from quantitative analysis, they currently have two options: either they use an expensive suite of tools or they try to build something on their own. With OpenSourcePV, we accompany their journey in quantitative signal detection allowing them to benefit from pre-built modules and building something customized to their specific needs and data sources.Starting Price: Free -
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Saama
Saama
Actionable insights, driven by the industry's #1 AI-powered clinical analytics platform, enable your teams to manage risk and improve performance across studies, systems, sites, and vendors. State-of-the-art clintech from Saama is designed to streamline your workflows, automate time-consuming processes, and improve collaboration across clinical operations, medical review, data management, biostatistics, and pharmacovigilance. Sponsors and CROs rely on Saama for data aggregation and artificial intelligence solutions that lead to better decision-making, eliminate delays, and significantly shrink drug development costs and timelines. Saama can put you on the fast track to clinical trial process innovation. When all your clinical data is in one place and updated in real time, life’s much easier for your ClinOps and medical review teams. Data Managers have been underappreciated for too long. Eliminate manual work so they can pay attention to the data points that matter. -
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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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Quanticate
Quanticate
Quanticate offers comprehensive pharmacovigilance services, including the provision and management of pharmacovigilance safety databases. A pharmacovigilance safety database serves as the central repository for individual case safety reports collected globally for a company's medicinal products. It is essential that these databases are up-to-date with the latest regulatory requirements and validated to meet international standards and business needs. Quanticate emphasizes the importance of selecting the right database by considering factors such as implementation and maintenance costs, hosting model availability (internal infrastructure, third-party hosting, or vendor cloud options), prior experiences, and compatibility with other systems. They caution that while many commercially available databases claim compliance with standards like ISO ICSR ICH-E2B, true compliance requires careful setup, validation, and management. -
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Flex Databases
Flex Databases
Document management and ensures regulatory compliance in clinical trials. By integrating AI and a unique "co-pilot" feature, our platform boosts efficiency while maintaining human oversight. Automated Filing with AI The AI assistant automates document classification and metadata assignment, reducing manual effort. Co-Pilot for Human Control The "co-pilot" feature allows users to set confidence levels for AI classification. Documents below the threshold are flagged for review, and users can adjust classifications, helping the AI improve. Key Benefits: Efficiency: AI automates tasks, allowing more focus on critical activities. Accuracy: AI and co-pilot oversight ensure data integrity and compliance. User-Friendly: An intuitive interface simplifies document management. Continuous Learning: AI improves accuracy with ongoing user feedback.Starting Price: $1300.00 -
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DF Literature Monitor
Datafoundry
DF Literature Monitor is an advanced AI-powered solution designed to automate the monitoring of vast amounts of literature and optimize safety vigilance processes. It integrates with major global and local literature sources for simultaneous article retrieval, employing semantic search to identify relevant articles efficiently. The platform features automatic de-duplication, extraction of minimum safety information, and auto-population of safety case forms, which can be submitted to safety databases in E2B or Excel/PDF formats with a single click. Additionally, it offers automated translation of abstracts and full articles into English. DF Literature Monitor includes configurable workflows to facilitate collaboration and quality control among pharmacovigilance teams. By leveraging this solution, teams can save up to 60% or more time and effort in the literature monitoring process while ensuring quality and compliance. -
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SlimEDC
Altamira
SlimEDC is a cloud platform for EDC – Electronic Data Collection. Retrospective and prospective studies, patient studies (ePRO), and market research projects are ready to launch in no time, using the provided study editor. SlimEDC is available as software, that is fully managed by the research sponsor or as a complex service, where the entire process up to the evaluation of data is provided by a professional SlimEDC team. SlimEDC is adapted to the EU environment and legislation. The respondents are contracted electronically, the software generates all the legally required reports for regulatory organizations. SlimEDC is ISO 9001 and 27001 compliant. Our team is BHBIA certificated and has undergone pharmacovigilance training. The legal and data security is subject to strict GDPR audits conducted by independent authorities. -
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Compier Literature Screening
Techsol Life Sciences
Compier Literature Screening is an AI-driven platform designed to assist pharmacovigilance professionals in efficiently screening abstracts, full texts, and translated articles to identify patients, authors, events, products, and safety-related information. The platform offers built-in integration with online biomedical databases such as Medline and supports bulk uploading of literature records from sources like Embase, conference presentations, and PDF journals. It performs automated duplicate checks for each literature search and utilizes validated AI models for automatic screening and annotation of entities. Users can configure scalable literature screening workflows tailored to specific requirements and global regulations. The system facilitates communication with third-party vendors to obtain full texts and includes built-in translation capabilities. It also integrates with safety systems, such as Oracle Argus Safety, to transmit ICSR-relevant articles. -
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Bibliovigilance
Bibliovigilance
Bibliovigilance is a search platform for pharmacovigilance literature that aims to streamline the process of monitoring scientific and medical publications for safety information. It offers a comprehensive database of significant national scientific publications across Europe and beyond, covering both human and veterinary products. The platform enables users to perform global searches by running queries in PubMed and accessing PRAC safety recommendations on signals, centralizing all literature searches in one location. Users can save their search queries, schedule automatic searches, and choose to search only for new articles since the last query, thereby saving time and reducing repetitive tasks. All searches are stored in a personal area, allowing users to see and document their search history at any time. The database is constantly updated, providing information on publications, the latest update dates, and the number of indexed articles, ensuring transparency in content. -
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InfoDesk
InfoDesk
Aggregate, enrich and monitor key information sources at scale with unparalleled integrations across premium licensed content, the open web, and internal intelligence sources. Identify the signal and eliminate the noise with the power of InfoDesk's information lab. Having supported global analysis teams for the past 25 years, we build powerful tools to make your lives easier. By leveraging our proven intelligence workflow, enhanced by enterprise-grade analysis tools, our solution streamlines monitoring and analysis, allowing professionals to focus on high-impact initiatives across regulatory, pharmacovigilance, competitive, market, and strategic intelligence functions. Centralize key information, streamline analysis, and empower stakeholders with trusted intelligence, powered by enterprise-grade AI. Get trusted intelligence into the hands of your stakeholders with our industry-leading deliverable engine. Drive engagement like never before with dynamic dashboards. -
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adWATCH
Atlant Systems
adWATCH - AE helps pharmaceutical organizations manage and report adverse events that occur during clinical trials. adWATCH - AE gives the reporter at a clinic, hospital, or investigative site a fast and effective means of generating and managing Adverse Event Reports (AERs) and reporting to the regulatory departments and government agencies. An adverse effect is a negative or dangerous effect experienced by a patient and caused by drugs and/or medical devices. Adverse event reporting requires the tracking of all medical complaint case information, resulting in the generation of MedWatch reports, CIOMS reports and additional reports for management. adWATCH - AE allows researchers, physician investigators, Contract Research Organizations (CROs), clinical trial specialists, and other health professionals to produce and file AERs in the FDA mandated MedWatch and/or CIOMS format.2 -
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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. -
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Altai Oncology Suite
Altai Oncology
All our software products are designed to be easy to use and learn. Intuitive user interfaces designed by Oncologists to save you time. Robust processes to enhance patient safety. Innovative modules to advance research. Automate your workplace, from planning chemotherapy orders to staff management. Our comprehensive solution for cancer centers to streamline Oncology workflow. Quickly generate accurate chemotherapy orders with ease. Our extensive and regularly updated protocol library with over 1000 protocols. Automatically calculates and verifies drug doses and infusion rates. Rigorously tested and CE marked. Doses verified twice. Drug-drug and drug-allergy interactions checked. Patient-drug matching with QR coded labels. Eliminate medication errors through patient and drug label matching. View the active chemotherapy order, patient diagnosis/stage, most recent lab results, and chemotherapy flowsheet in one screen.Starting Price: $99 per month -
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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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LifeSphere Safety
ArisGlobal
LifeSphere Safety offers the only unified, next-generation SaaS Safety platform in production, built to enable touchless case processing, scalable compliance, and standardized global pharmacovigilance workflows. Drive transformative change with industry-leading capabilities, including the latest innovations in automation, analytics, and GenAI technologies powered by LifeSphere NavaX. Drive significant efficiency gains through touchless case processing by leveraging robust, production-ready automation and artificial intelligence to streamline repetitive safety tasks. Operate confidently in any market with the most robust turnkey support for global and regional regulations, including regular cloud upgrades to ensure future-proof compliance. Turn safety into a value center by leveraging powerful, easy-to-use tools for reporting and dashboarding, operational benchmarking, and intelligent signal analysis. -
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Orbit
Orbit
Orbit is a strategic platform designed to enhance patient safety by assisting small, medium, and large biopharma companies in scaling their safety operations across global markets. It offers innovative solutions for global pharmacovigilance, safety, and risk management oversight, aiming to increase global quality, demonstrate compliance, improve productivity and efficiency, and provide meaningful oversight of traditionally complex and siloed processes. Key features include risk management and minimization, which tracks global risk management plan commitments and supports local additional risk minimization measure implementation; safety data exchange and pharmacovigilance agreements management, allowing oversight across global partnerships; signal and surveillance management, covering signal management from strategy through detection activities, signal assessment, and tracking. -
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biologit MLM-AI
biologit
Biologit offers a comprehensive suite of software and services designed to enhance safety surveillance across various industries. Their flagship product, biologit MLM-AI, is an all-inclusive global and local medical literature monitoring platform powered by AI. This scientific literature monitoring platform is simple to use, fully web-enabled, and validated for compliance, providing productivity gains for human and veterinary pharmacovigilance. Key features include integrated search and configurable literature screening workflows delivering up to 70% productivity gains powered by AI, a flexible and validated SaaS platform that is GxP-ready and CFR-11 compliant, and a database hosting major global and local literature sources with automatic article de-duplication. In addition to its software solutions, Biologit offers consultancy services covering pharmacovigilance, veterinary pharmacovigilance, and more. -
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Prescription Pad
CompuRx Infotech
Safe, first-rate, foolproof prescription writing facility. Comparative Analysis Of Patient's Medical History. Check Drug Interaction & Brand Interaction. Automatic drug safety checks. Enables searching suitable drugs & brands. Keep record of every visit of individual patient in chronological order. A new Prescription would take even less than 2 minutes to complete. Scan patient's past history, family history and give you useful tips. Check for drug safety at individual disease level also like in case of G6PD, PORPHYRIA, HYPERTENSION, COPD etc. Makes the life of both the doctors and patients easy, comfortable and organized. Complete prescribing information of nearly 70,000 Brands of Indian, British & American drug database Pharmaceuticals. Full monograph of nearly 3,000 drugs (generic drugs) compiled from PDR of U.S.A., Martindale book of pharmacology, British National Formulary etc. Contains complete diagnostic information, differential diagnosis & treatment protocols.Starting Price: $170 one-time payment -
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ez-DIMS
Alpha Clinical Systems
Drive study efficiency, regulatory compliance, and patient safety with Alpha Clinical Systems' electronic drug inventory management system (DIMS). Reduce site errors and workload while gaining real-time transparency. A comprehensive web-based system, ez-DIMS streamlines drug and device distributions at the site to eliminate transcription errors. Integrated with ex-SourceDocx, automatically accounts for supply disbursements, providing real-time visibility of drug inventory. Replace slow, error-prone, manual processes with user-friendly ez-DIMS. Reduce site workload with user-friendly scanners to quickly, easily, and accurately record study supply inventory and accountability at the patient, site, and study levels. Drug inventory violations at the site are the second most common regulatory inspection finding. Reduce medication assignment/dispensation errors by leveraging QC cross-checks between ez-DIMS and ez-SourceDocx. -
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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. -
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WellaHealth Engage
Wella Health
Available on Android, desktop or the web, we help you grow through innovative automated pharmaceutical care. Record & retrieve patient drug history rapidly. Avoid fines, obey pharmacy record-keeping laws. Know & care for your patients better. Auto follow-up patients with SMS drug reminders. Target segregated patient groups with smart bulk SMS. Respond to SMS messages to keep patients loyal. Check over 14,000 drug-drug interactons. Manage patient refills of chronic medications. View stats and receive regular updates on your usage. Connect to your Quickbooks inventory/ POS system. Gain an online dedicated webpage to attract patients. Get Help delivering routine primary care to patients. Give better-personalized drug information. Adhere to international best practice.Starting Price: $10.00/month -
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iMed e-Rx
iMedWare
iMed e-Rx electronic prescription system starts from $43/month and can be used for writing both legend and EPCS compliant prescriptions. Which is Certified for e-Prescribing in all States. Our software has Electronic prior authorization and it has Formulary support. Our key highlights are Drug-Drug, Allergy, and Disease interaction checking, Database of drug stores with frequent updates, Drug therapy monitoring, 24/7 monitoring of script delivery and so on.Starting Price: $43 per month -
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HelioMetrics
HelioMetrics
Diversion of controlled substances can occur anywhere in the pharmaceutical supply line, but more predominantly in hospital pharmacies and healthcare delivery. HelioMetrics Healthcare Rx Drug Diversion Analytics Software can help speed up identification of drug diversion activity, accelerate your diversion investigations and reduce associated drug diversion costs in healthcare. Look in the news and you are sure to find something about the “opioid epidemic” and how there are problems everywhere with healthcare workers and pharmacists stealing these and other drugs. In some cases, the healthcare worker has even caused HIV and Hepatitis C concerns. Some of these cases have moved into the legal world with hospitals facing hundreds of lawsuits from former patients. Not to mention the fines that the DEA is now handing out. The risk of drug diversion is real, not only from a patient safety issue, but from financial issues for the healthcare facility. -
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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.