DrugCard
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About
DrugCard is an AI-powered platform designed to streamline pharmacovigilance processes. It automates the screening of local medical journals in multiple languages (100+), significantly reducing the time and resources required for drug safety monitoring. DrugCard boasts high accuracy OCR technology (99%) and provides weekly reports, enhancing efficiency and compliance. The platform is designed for CROs, MAHs, and freelancers, offering time savings of up to 70%. Key features include continuous monitoring, traceability, accuracy, scalability, multilingual and multi-regional support, cost-effectiveness, and AI-driven insights.
Platform
Features
• streamlines drug safety routines
• ai-enabled data intelligence
• weekly summary reports
• high accuracy ocr (99%)
• time savings (50-70%)
• automated literature screening
• multiple language support (100+)
• local medical journal screening
FAQs
How much time can I save when using DrugCard?
Based on our customer feedback 50-70% time-savings could be achieved. However, we strongly welcome that planned time and cost savings were calculated for each project individually. Suppose it takes 30 minutes to read and another 5 more minutes to properly record evidence of reading, with DrugCard it would take only 3 minutes max, which is almost 10 times less.
Can DrugCard recognize poorly scanned texts?
Yes, we often face requests from our customers to help them screen printed hard copies of journals with scan quality being far from perfect. We use our own propitiatory OCR technology which delivers up to 99% accuracy of average quality scanned texts.
Can DrugCard screen local medical journals in local languages?
Yes, screening medical literature in local languages is DrugCards main competitive strength. To date we successfully read 100+ languages and already covered 400+ local journals. It means you can add search keywords in Greek, Hindu, Arabic, Japanese hieroglyphics, you name it.
Can I have weekly reports with all data collected in a week?
Yes. Once DrugCard identifies new drug mentioning in any local journal you will get an instant notification by email. On top you will receive weekly summary reports to make your life easier during audits and regulatory inspections.
How long does it take to add journals in a new country?
On average it takes up to 2-3 weeks. Of course it depends on a particular country and a number of journals to be added. We once managed to add 100 custom journals for one of our clients in just a matter of 1 month. But again, on average you should consider time to add new pack of journals in just 2-3 weeks.
How long could it take for me to develop such a system internally?
It took us one year and a team of 5 people to develop the core. And 2 more years and 6 more people to make the platform friendly, reliable, bug-free, responsive and regulatory compliant. Hypothetically you could follow the same journey, but developing such a platform just for 1 company would be very costly and counter effective.
With DrugCard can I manage local medical literature screening without any staff?
We have seen cases where a significant part of daily routine of PV specialists was freed and redirected to more intelligent work like signal detection, risk assessment, ICSR & case follow up activities, quality control, etc. It is our strong belief that such rare expertise as pharmacovigilance should never be used for something that could be automated.
What are your unique strengths compared to your competition?
We see our main competition to be manual literature screening processes and lack of willingness to change. Even though some companies say they are happy with reading journals from cover to cover, our undisputed strengths would be (1) three to five times more hits discovered, (2) 50-70% time saved on screening (3) 99% accuracy of keywords recognition of average scanned texts. And since every project is different we invite you to have a discussion and design your specific use case.
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