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Software used to collect data to prevent, assess, and respond to adverse drug reactions. - Automate workflows for case registration, record tracking, and aggregate reporting - Use tools to perform risk-benefit analysis, data mining, and signal detection - Provide visibility for data insights, risk profiles, and surveillance - Meet regulatory requirements with real-time safety intelligence
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IQVIA Vigilance Platform is built on a platform-of-platforms strategy, delivering an integrated, comprehensive SaaS platform that simplifies pharmacovigilance processes while boosting speed, accuracy, and efficiency. Built by safety experts to meet today's and tomorrow’s challenges, leveraging IQVIA’s domain expertise and external technologies, IQVIA Vigilance Platform coverts the entire safety process. IQVIA Vigilance Platform is an end-to-end solution, including six modules: • IQVIA Vigilance Detect • IQVIA Vigilance Collect • IQVIA Vigilance Intake • IQVIA Vigilance Case • IQVIA Vigilance Analytics • IQVIA Vigilance Signal
PvEdge drug safety database provides comprehensive analyses of adverse events arising from the use of pharmaceutical products (Drug, Medical Device or Therapy, Vaccine). It is an advanced Pharmacovigilance solution that helps combat the complexity of the safety data and comprehensively caters to all risk management requirements on a single platform, ensuring global regulatory compliance.
DF Literature Monitor is a modular and scalable Literature Monitoring solution that can be integrated with leading safety databases and signal management products. Our state-of-the-art technology uses AI models to automate the monitoring of vast amounts of literature. With features like semantic search to retrieve relevant articles from all the major global and local literature databases simultaneously, de-duplication, extraction of minimum safety information and populating safety case forms, one click submission of case forms to Safety Database in E2B or Excel/PDF formats, automated translation of abstracts and full articles to English, pharmacovigilance teams can save up to 60% or more time and effort in literature monitoring process while ensuring quality and compliance.
DF mSafety AI is a cloud-based safety platform that uses the power of AI/ML and automation to deliver efficiencies and a great user experience in Safety Case Management and Signal Detection for Drugs, Cosmetics, Neutraceutical and Medical Devices. DF mSafety AI is built on Datafoundry’s Integrated Cloud Platform - DF Safety 4.0 which supports scalable and secure AI/ML driven Safety Case and Signal Management, pre-built connectors to enterprise systems, adhere to regulatory requirements and industry standards. Built by industry experts with decades of experience joining hands with a team of world class data scientists and ML pioneers, DF mSafety AI is the solution to address your key challenges in Safety Management – from case intake and triage through medical review and regulatory submission. #RWE #RWD #Safety #PV
DrugCard provides full-regulatory compliant SaaS to help pharmacovigilance teams, trimming literature screening time by 70% and generating deeper insights about drug safety using sophisticated parsers and AI-tech Key features: • Automated literature screening with weekly search reports • 950+ local medical journals in 50+ countries • Global literature monitoring via Pubmed • Instant notifications with new drug safety information • GVP, CRF 21 part 11, GAMP5 compliance • Data security SOC type 2/3 and ISO/IEC 27001:2013 • Traceable workflow with user roles • Accessibility 24/7 and customer support To start 14 days trial, feel free to connect: sales@drug-card.io
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‘AccelSafety’ is a comprehensive pharmacovigilance platform of Techsol built around Oracle Argus Safety application to address business needs of unified collection, medical assessment and regulatory reporting of clinical & post-marketing safety surveillance data. Our fully-managed cloud solution facilitates emerging biopharma, device manufacturers and service providers to manage safety data and take informed business decisions in alignment to global compliance requirements.
Biologit MLM-AI is a complete literature screening platform built for pharmacovigilance and medical devices safety monitoring teams. Regulatory searches are challenging to implement and operate and manual workflows grow in complexity and risk very quickly. With biologit's flexible workflow, unified scientific database, and unique AI productivity features, safety monitoring teams achieve deliver fast, inexpensive, and fully traceable results for any screening needs. ✔️ Integrated global and regional scientific literature databases out of the box ✔️ Fully validated and audit-ready SaaS compliant with industry guidelines (GVP, CFR-11) ✔️ 70% productivity gains powered by AI ✔️ Configurable workflows for all safety monitoring requirements: ICSR, signal detection, PSURs, EU MDR/IVDR, FDA safety monitoring requirements
PVSEARCH is a validated data management system, developed by Owlpharma Consulting Lda., for pharmacovigilance professionals. It’s a software as a service (SaaS), intended to support the medical literature screening activity. PVSEARCH design concept defines it as a scientific literature repository connected to a robust search engine. The search engine is configurable with predefined inputs, which allows our clients to identify their required search terms.
dezzai Sentria is an AI-based platform for ICSR management and PMS medical literature monitoring. It uses semantic AI technology to scale-up the capacity, speed and precision of adverse event management by following the next steps: 1. Search, extraction and pre-screening of multi-channel adverse event reports. 2. Detection, classification, and validation of potential ICSR events. 3. Document, track, and registration of ICSR cases
SafetyEasy™ is designed to streamline your pharmacovigilance, medical device vigilance, cosmetovigilance and nutrivigilance processes quickly and effectively. Maintaining safety data is a mandatory regulatory requirement. Yet despite the undoubted benefits it brings, it can be a time-intensive and costly process that ultimately contributes little to bottom-line revenue. Built specifically to support the E2B(R3) EudraVigilance system and MedDRA coding standards, SafetyEasy™ handles the reporting and management of all serious and non-serious adverse events. Its future-proof approach is able to generate PSUR, PBRER, and DSUR documentation and is ready for forth-coming standards such as IDMP. It also supports eMDR XML file creation. Through an EMA certified gateway, SafetyEasy™ provides you with a direct link to the regulatory authorities, eliminating the need for manual submission of reports.