Alternatives to PVSEARCH
Compare PVSEARCH alternatives for your business or organization using the curated list below. SourceForge ranks the best alternatives to PVSEARCH in 2026. Compare features, ratings, user reviews, pricing, and more from PVSEARCH competitors and alternatives in order to make an informed decision for your business.
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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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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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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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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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Dialog
Clarivate
Dialog offers a modular, end-to-end pharmacovigilance literature monitoring solution that supports organizations tasked with drug safety reporting by streamlining and automating the entire literature triage process. It provides access to over 140 authoritative scientific and medical literature databases, such as MEDLINE, Embase, and Biosis, standardizing content across sources to ensure consistent precision search, deduplication, and structured XML output. The DialogML engine employs artificial intelligence to rank search results by patient-safety relevance, highlight key safety concepts, and tag references related to ICSRs (Individual Case Safety Reporting), aggregate reports (PBRER, PSUR, DSUR), and safety signals, so reviewers can rapidly identify high-priority articles. The Dialog Alerts Manager simplifies alert creation and management, offering bulk editing, audit trails of search strategy changes, scheduling flexibility, and delivery history tracking. -
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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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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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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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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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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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PvEdge
Sarjen Systems
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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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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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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SciSpace BioMed Agent
SciSpace
SciSpace BioMed is a domain-native AI “co-scientist” for biomedical research that combines a vast literature database with 150+ integrated bio-tools and 100+ academic databases and software suites to streamline complex research workflows, from genomics and single-cell analysis to drug discovery and clinical genomics. It enables researchers to ask natural-language questions, ingest datasets, interpret variants or multi-omics data, design cloning or wet-lab workflows, reason about clinical or disease biology, and generate publication-ready outputs (e.g., figures, tables, and presentations) with full transparency and citations. Users can interact with scientific papers via “chat with PDF,” highlight confusing text, math, or tables, and get clear explanations, ideal for understanding difficult methods or concepts. For literature review or exploratory research, its AI-driven semantic search accesses millions of papers and returns citation-backed summaries.Starting Price: $12 per month -
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Cure AI
Cure AI
Cure AI is an advanced medical research engine that utilizes artificial intelligence to provide comprehensive access to over 26 million scientific articles from PubMed. It offers AI-powered natural language search capabilities, allowing users to input research queries in conversational language, which the system interprets to deliver precise results. The platform features advanced search parameters, enabling users to refine results by journal, publication date, and other criteria for tailored research needs. Cure AI ranks evidence based on quality and relevance, considering factors such as journal h5-index, citation count, and publication type, ensuring that users receive the most pertinent and verified information. Additionally, it provides seamless navigation between AI-generated insights and primary literature sources, facilitating efficient literature review and analysis. The platform includes quick citation tools, allowing users to copy or share citations with a single click.Starting Price: $15 per month -
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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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Scopus
Elsevier
Scopus offers free features to non-subscribed users as Scopus Preview. Researchers use Scopus Preview to assist with research, such as searching for authors and learning more about Scopus content coverage and source metrics. Scopus is an abstract and citation database of peer-reviewed literature including scientific journals, books, and conference proceedings. Scopus provides a comprehensive overview of worldwide research output in the fields of science, technology, medicine, social sciences, and arts and humanities. Scopus is the largest abstract and citation database of peer-reviewed literature: scientific journals, books and conference proceedings. Delivering a comprehensive overview of the world's research output in the fields of science, technology, medicine, social sciences, and arts and humanities, Scopus features smart tools to track, analyze and visualize research. You can make sure that critical research from around the world is not missed when you choose Scopus. -
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Sorcero
Sorcero
Sorcero is an AI-powered platform designed to transform complex medical data into actionable insights for the life sciences industry. With its suite of products, including Medical Insights Management, Intelligent Publication Monitoring, Plain Language Summaries, and Intelligent Systematic Literature Review, Sorcero unifies and analyzes unstructured and structured data from a variety of sources. By using AI to analyze medical themes, notes, and research, Sorcero delivers high-quality, easy-to-understand answers to complex medical questions, helping teams in Medical Affairs, Pharmacovigilance, and Regulatory Affairs drive more informed decisions. The platform supports rapid literature monitoring, content generation, and evidence-based decision-making, ultimately boosting patient outcomes and enhancing operational efficiency. -
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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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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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Edison Scientific
Edison Scientific
Edison Scientific is an AI platform designed to automate and accelerate scientific research, enabling users to move from hypothesis to validated results within a single environment. The platform integrates literature synthesis, data analysis, and molecular design workflows, allowing research teams to complete end-to-end scientific investigations at dramatically increased speed. At its core is Kosmos, an autonomous research system that performs hundreds of research tasks in parallel, transforming multimodal datasets into comprehensive reports with validated findings and publication-ready figures. Kosmos synthesizes scientific literature, public databases, and proprietary datasets, identifies novel therapeutic targets, uncovers biological mechanisms, and supports the iterative design and optimization of molecular candidates. Validated in real research settings, Kosmos has demonstrated the ability to achieve results that typically require months of human effort in a single day.Starting Price: $50 per month -
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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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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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MEDLINE
National Library of Medicine
MEDLINE is the National Library of Medicine’s (NLM) premier bibliographic database that contains more than 29 million references to journal articles in life sciences with a concentration on biomedicine. A distinctive feature of MEDLINE is that the records are indexed with NLM Medical Subject Headings (MeSH). MEDLINE is the primary component of PubMed, a literature database developed and maintained by the NLM National Center for Biotechnology Information (NCBI). MEDLINE is the online counterpart to the MEDical Literature Analysis and Retrieval System (MEDLARS) that originated in 1964 (see MEDLINE history). The majority of journals are selected for MEDLINE based on the recommendation of the Literature Selection Technical Review Committee (LSTRC), an NIH-chartered advisory committee of external experts. Time coverage: MEDLINE includes literature published from 1966 to present, and selected coverage of literature prior to that period. -
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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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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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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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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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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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K2C PSMF Solution is a modern approach to the management of the Pharmacovigilance System Master File. This document typically requires periodic updates as per significant changes in the pharmacovigilance process. These changes require that multiple company roles are involved in editing a document that is composed of paragraphs and annexes that are all the time same because fixed by regulations. However co-editing is complex; in addition, part of the content should be reserved to some editors and even not available to other contributors. K2C solution allows handling the distinct paragraphs and annexes as single documents, then it offers the possibility to create the PSMF document as a merge of various source documents. K2C PSMF Solution includes management of PSMF contributions (paragraphs and annexes) as distinct documents; management of access rights for viewing or editing of PSMF contributions; and management of the entire lifecycle.Starting Price: €8,500 one-time payment
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PubMed
PubMed
PubMed® comprises more than 35 million citations for biomedical literature from MEDLINE, life science journals, and online books. Citations may include links to full-text content from PubMed Central and publisher websites. PubMed is a free resource supporting the search and retrieval of biomedical and life sciences literature with the aim of improving health–both globally and personally. The PubMed database contains more than 35 million citations and abstracts of biomedical literature. It does not include full text journal articles; however, links to the full text are often present when available from other sources, such as the publisher's website or PubMed Central (PMC). Citations in PubMed primarily stem from the biomedicine and health fields, and related disciplines such as life sciences, behavioral sciences, chemical sciences, and bioengineering. MEDLINE is the largest component of PubMed and consists primarily of citations from journals selected for MEDLINE.Starting Price: Free -
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Causaly
Causaly
Leverage the power of AI to expedite the journey from bench research and laboratory insights to the launch of life-changing therapies. Gain up to 90% in research productivity by reducing your reading time from months to minutes. Cut through the noise with a high-precision, high-accuracy search to navigate the ever-growing volume of scientific literature with ease. Save time, reduce bias and increase odds of novel discoveries. Deeply explore disease biology and conduct advanced target discovery. Causaly’s high-precision knowledge graph consolidates evidence from millions of publications, making deep, unbiased scientific exploration possible. Rapidly navigate biological cause-and-effect relationships without being an expert. Get a view of all scientific documents and uncover hidden connections. Causaly’s powerful AI machine reads millions of published biomedical literature to support better decision-making and research outcomes. -
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Reaxys
Elsevier
Reaxys is a web-based tool developed by Elsevier for retrieving information about chemical compounds and data from published literature, including journals and patents. The platform provides access to chemical compounds, reactions, properties, related bibliographic data, substance data with synthesis planning information, and experimental procedures from selected journals and patents. Launched in 2009 as the successor to the CrossFire databases, Reaxys was designed to offer research chemists access to current and historical information in organic, inorganic, and organometallic chemistry through an intuitive interface. The platform covers over 200 years of chemistry, abstracted from thousands of journal titles, books, and patents. Its content includes data from selected journals and chemistry patents, focusing on entries that have a chemical structure, are supported by experimental facts, and have credible citations. -
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AnswerThis
AnswerThis
AnswerThis is a scientific discovery platform that reduces weeks of manual research work to hours. Instead of manually searching, reading, and organizing dozens of papers, researchers use AnswerThis to find the most relevant work, see how ideas are connected, and get comprehensive answers to complex scientific questions with line by line answers. This allows them to map research gaps, analyze trends, and draft literature reviews far faster, all while building a searchable library of their own research materials. Thousands of scientists already rely on AnswerThis for the entire workflow from ideation to publication. -
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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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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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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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WisPaper
WisPaper
WisPaper is an AI-driven research assistant that helps users search, filter, and synthesize academic papers and literature quickly and intelligently. Its “Scholar Search” feature acts like an agent: you issue queries about a topic and WisPaper scours research databases to surface the most relevant papers, abstracts, metrics, and insights. Rather than just returning lists, WisPaper lets you screen and filter results by relevance, date, citations, and impact, providing summaries and context to help you zero in on what matters. It also supports concept exploration, if you’re unsure of the exact terms, Wispaper can suggest related keywords or begin from broad ideas and help narrow them. The interface is built to streamline the literature review workflow, reducing the time spent manually digging through search engines, reading many abstracts, and cross-checking sources.Starting Price: Free -
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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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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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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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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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scienceOS
scienceOS
scienceOS is an AI-powered research platform built to accelerate scientific literature workflows by giving researchers fast, reliable access to a massive database, more than 225 million research papers via a chat-based interface. The core “AI science chat” lets you ask questions, get answers grounded in published literature, and even generate tables or diagrams summarizing findings. If you upload PDFs, the “multi-PDF chat” can parse up to eight documents per session and extract key passages, figures, and tables to help you digest papers quickly; it can also generate structured summaries of papers (e.g., intro, methods, conclusions), highlighting main findings, limitations, and key data. Alongside that, scienceOS includes an AI reference manager; you can store and organize up to 4,000 PDFs or citations in a personal or shared library, import external references (e.g., from Zotero), and chat with your own collection, useful for drafting literature reviews and building bibliographies.Starting Price: $7.95 per month -
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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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Google Patents
Google
Patents from around the world, translated. Plus technical papers and books, are organized and labeled automatically. Search for prior art, all in one place. Understand results, with images, PDFs, and citations. Security technology and the Privacy Policy protect your data. Search and read the full text of patents from around the world. Google Patents includes over 120 million patent publications from 100+ patent offices around the world, as well as many more technical documents and books indexed in Google Scholar and Google Books, and documents from the archive. New ideas are often published either as patent applications or in academic journals. If you are searching for prior art to a patent application, it is critical in many fields to also search for non-patent literature to get a complete view of the state of the art. Patents with only non-English text have been machine-translated to English and indexed, so you can search patent publications using only English keywords. -
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Resea.AI
Resea.AI
Resea AI is a full-featured academic research assistant that autonomously plans, conducts, and writes in-depth academic tasks from literature review to report drafting. It connects seamlessly with major scholarly databases such as Google Scholar, PubMed, and arXiv to source trusted research, then employs its proprietary “Think and Research” engine to determine research direction, core concepts, and writing angles through multi-stage inquiry. Feeding into its AI writing editor, Resea AI is capable of generating documents of unlimited length (even up to 50,000 words), and offers interactive editing for fast refinements. It ensures academic rigor through support for dozens of citation formats with accurate source indexing. It evaluates performance with benchmarks like xBench‑DeepSearch that measure deep research capabilities. Additional use cases include systematic literature reviews, academic outlines, content synthesis, reviewer-perspective feedback, and more.Starting Price: $12 per -
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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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DistillerSR
DistillerSR Inc.
Automate every stage of your systematic literature review to securely produce evidence-based research faster and more accurately. DistillerSR automates the management of literature collection, triage, and assessment using AI and intelligent workflows. DistillerSR makes any project, large or small, simpler to manage and configure to produce transparent, audit ready, and compliant literature reviews. Search more efficiently with DistillerSR’s integrations with data providers, such as PubMed, automatic review updates, and AI-powered duplicate detection and removal. Automatically import newly published references, always keeping literature reviews up-to-date. Detect and remove duplicate citations preventing skew and bias caused by studies included more than once. Reduce your screening burden by 60% with DistillerSR. Start working on later stages of your review sooner and more accurately by finding relevant references faster and addressing conflicts more easily.Starting Price: $215 per user per month
