DrugCard

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About
DrugCard is an AI-driven automated pharmacovigilance platform designed to streamline drug safety routines for the pharmaceutical industry. The software addresses the increasing regulatory pressure and rising costs associated with manual safety monitoring by providing a continuous, traceable, and transparent solution for identifying adverse events. By automating the screening of local medical literature, the platform helps organizations maintain compliance with Global Pharmacovigilance Practices (GVP) and other international regulatory requirements. The platform leverages advanced artificial intelligence to monitor over 2,200 local medical journals across 112 countries. It is capable of processing information in more than 100 languages, allowing for a comprehensive and holistic approach to safety data collection. Beyond simple keyword matching, DrugCard is designed to recognize and extract data from poorly scanned texts, ensuring that critical information is not missed due to low document quality. Users receive automated weekly reports and have access to an adverse event database, which centralizes findings and simplifies the transition from raw data to actionable insights. This solution is specifically tailored for Contract Research Organizations (CROs), Marketing Authorization Holders (MAHs), and freelance pharmacovigilance specialists. For CROs, the automation allows for the management of multiple PV projects simultaneously without a proportional increase in headcount. MAHs benefit from the platform's ability to ensure search results are exhaustive, meeting the high standards expected by regulatory bodies during audits. By reducing the time spent on manual journal reading by approximately 60%, the tool allows safety experts to focus on higher-value tasks such as signal detection, Risk Management Plans (RMPs), and Periodic Safety Update Reports (PSURs). What distinguishes DrugCard in the pharmacovigilance market is its focus on local literature monitoring, a task often overlooked by global databases but required by many regional health authorities. The platform provides a CAPEX-free investment model, making it accessible for firms looking to modernize their tech stack without significant upfront infrastructure costs. By combining multi-region supplier coverage with a multi-language processing engine, DrugCard offers a scalable way for pharmaceutical companies to enter new markets with confidence in their safety monitoring capabilities.
Pros & Cons
Reduces literature screening time by 60% compared to traditional manual methods.
Supports monitoring in over 100 languages across 112 countries.
Capable of processing and extracting data from poorly scanned medical journal texts.
Provides a centralized adverse event database for better traceability and transparency.
Automates the generation of weekly reports for regulatory compliance.
Pricing information is not publicly listed and requires a custom demo or contact.
Platform focus is primarily on literature monitoring rather than full clinical trial management.
Integration into existing pharmacovigilance systems requires a consultation with their experts.
Use Cases
CRO managers can automate local literature screening across multiple client projects, improving search accuracy while reducing manual labor hours.
Pharmacovigilance specialists can transition from manual journal reading to high-priority tasks like signal detection and PSUR preparation by using AI-generated reports.
Marketing Authorization Holders (MAHs) can ensure global regulatory compliance and audit readiness by maintaining a transparent and traceable record of all safety data.
Platform
Features
• support for 100+ languages
• full gvp regulatory compliance
• poorly scanned text recognition
• integrated adverse event database
• automated weekly safety reports
• monitoring across 112+ countries
• coverage of 2200+ local journals
• ai-driven automated screening
FAQs
How much time can be saved by using DrugCard?
Users typically experience a 60% reduction in time compared to a human-only approach. This efficiency gain allows pharmacovigilance teams to reallocate their focus toward strategic tasks like signal detection and safety data assessment.
Does the platform support local medical journals in different languages?
Yes, DrugCard monitors over 2,200 local journals in more than 100 different languages. This wide coverage ensures that Marketing Authorization Holders can maintain compliance across 112 countries.
Can the AI handle documents that are not perfectly clear?
The system is specifically designed to recognize and process data from poorly scanned texts. This capability ensures that valuable safety information is captured even when the source material is of lower visual quality.
How frequently are reports generated by the system?
DrugCard allows users to receive weekly reports containing all the data collected during that period. These automated reports help streamline the reporting process and ensure that safety routines remain continuous and regular.
Is there a way to test the platform before committing?
Potential users can request a demo or start a free trial to evaluate the platform's features. This allows organizations to see how the AI integrates into their existing pharmacovigilance systems.
Pricing Plans
Custom
Unknown Price• Scalable to new markets
• Multi-language support
• Continuous monitoring
• Weekly reports
• Adverse event database access
Free Trial
Free Plan• Starting a free trial
• Access to platform features
• Literature screening demonstration
Job Opportunities
There are currently no job postings for this AI tool.
Ratings & Reviews
No ratings available yet. Be the first to rate this tool!
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