Driving Pharmacovigilance forward with AI-enabled Data Intelligence

    Streamline your drug safety routines with us

    User interface preview

    Our customers

    Pharmacovigilance evolving rapidly.
    We understand your pressures

    What has changed in the last 3-5 years and how this affected
    the industry
    AI-Competition

    Growth has slowed down as new aggressive?entrants with AI-tech shake the status quo.

    Tech / digital age

    New heavy investments have longer paybacks while the change cycles have shrinked.

    Audits / regulatory pressure

    The number of audits has increased. More and more non-compliance cases and mitigations.

    People costs are rising

    Good people leaving increases the retention costs, while the new talent costs more. Heavy investments in staff training and onboarding new talents.

    New pinches strike harder
    and harder

    People are stressed and it is hard to predict their buying behaviors. Adverse reactions become more frequent.

    Entering new markets

    Entering new markets has become longer, less predictable, and more costly.

    Global pressures dictate new requirements to drug safety processes

    About DrugCard platform in numbers

    100+
    Languages

    Supported by DrugCard

    83+
    Countries

    Medical journals coverage

    1500+
    Local journals

    Countiniously monitored

    70%
    Time savings

    Compared to human-only approach

    Our Management Team

    Artem Horilyk

    Chief Product Officer

    Dmytro Horilyk

    Chief Executive Officer

    Myroslav Demchun

    Chief Technology Officer

    DrugCard solution designed for

    CROs can manage more PV projects and improve screening results

    When pharma outsource PV processes to CROs, they expect the highest quality and maximum search results to ensure full compliance with regulatory requirements. CROs can no longer guarantee the best results if they continue to read journals from cover to cover manually. Progressive CROs continuously discover innovative methods and tools to make their pharma customers fully compliant and satisfied. ? ? ??

    Testimonials

    Trusted customers that can provide everything you need to generate awareness, drive traffic, connect
    photo_2022-10-13_14-04-04
    5/5

    "Phenomenal tool that saves time and does local literature screening instead of you. The cost is minimal in comparison to the level of results it can give."

    — Valentina Eremenko
    PV Freelancer
    Rectangle 4705 (2)
    facebook (1) 1
    5/5

    DrugCard has helped our team put MLM process on autopilot. It is simple to use and free up time for other tasks. I would highly recommend it to all PV services vendors

    Natalka Ischuk
    Owner, PV Systems
    Rectangle 4705
    facebook (1) 1
    5/5

    We need a solution for screening local literature from CIS countries. And your product is exactly what we need.

    Vladyslav Vesna
    Deputy QPPV, PV Team Leader Farmak

    Frequently Asked Questions

    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.

    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.

    Yes, screening medical literature in local languages is DrugCards main competitive strength.? To date we successfully read 100+ languages and already covered 1500+ local journals. It means you can add search keywords in Greek, Hindi, Arabic, Japanese hieroglyphics, you name it.

    Yes. Once DrugCard identifies a 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.

    On average, it takes up to 2-3 weeks. Of course, it depends on a particular country and the 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 a new pack of journals in just 2-3 weeks.

    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 counterproductive.

    We have seen cases where a significant part of the 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.

    We see our main competition to be manual literature screening processes and a 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.

    Enhance Your Pharmacovigilance

    Unleash the power of AI, automation and traceability with DrugCard
    Request a demo
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