DrugCard

Skip to content AI-Driven Automated Pharmacovigilance Solutions Streamline your drug safety routines with us Contact us Our customers Pharmacovigilance evolving rapidly. We understand your pressures What has changed in the last 3-5 years and how this affectedthe 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 harderand 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 With DrugCard these requirements will be under control: Continuous and regular Traceable and transparent Accurate, complete, holistic Scalable to new markets Multi-language Multi-region suppliers CAPEX free investments Cost-effective About DrugCard platform in numbers 100+ Languages Supported by DrugCard 121+ Countries Medical journals coverage 2200+ Local journals Countiniously monitored 60% 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 CROsMAHsFreelancers 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. Talk to us In-house local literature screening for MAHs Outsourcing of literature screening to CROs has become so widespread and common in the last 5-7 years. However, we at DrugCard strongly believe that literature screening could be done more effectively, either in-house, at both a global and local level, or with very few contractors. Managing multiple CROs across several countries is becoming a nightmare for any MAH, creating compliance and reputation risks. DrugCard, its trusted partners, and loyal customers actively promote upgrading obsolete screening practices and help install new standards, high-performance screening methodology, and tools. Talk to us Free up time for other activities With DrugCard, freelancers providing literature screening and other outsourcing services can save up to 70% of their precious time and use it for other value-adding activities such as consulting, research, quality assurance, etc. Higher productivity, less work, more revenues! Talk to us Testimonials Trusted customers that can provide everything you need to generate awareness, drive traffic, connect DOVILĖ MARCINKĖHead of Global Drug Safety Unit and QPPV Read More DrugCards stands out as a mandatory operation tool, enabling our presence and activities with efficiency, cost saving and compliance with GVP regulations and other applicable requirements. Jaime RuizSenior Pharmacovigilance Specialist Read More No more spending hours reading articles, since we started working with Drugcard we are more productive in other tasks. It is a very reliable tool that has certainly helped us a lot in the team. 100% recommendable! Cristina RuizPV Project Manager Read More Drugcard has allowed us to automate a critical process in our work: local literature monitoring. Not only does it save time, but it also captures more information than we could gather manually, and with the time saved, we can now focus on high-priority tasks such as signal detection, PSURs, RMPs, and much more. Previous Next Frequently Asked Questions 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 1500+ local journals. It means you can add search keywords in Greek, Hindi, Arabic, Japanese hieroglyphics, you name it. Can I have weekly reports with all data collected in a week? 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. 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 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. 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 counterproductive. With DrugCard can I manage local medical literature screening without any staff? 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. What are your unique strengths compared to your competition? 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 Schedule a meeting Request a demo Menu Request a demo Name* Surname* E-mail* Phone number* Company* This site is protected by reCAPTCHA and the Google Privacy Policy and Terms of Service apply. Send ↑ --- We value your privacyBy clicking “Accept All Cookies”, you agree to the storing of cookies on your device to enhance site navigation, analyze site usage, and assist in our marketing efforts.Cookies Settings Accept All Cookies Customize Consent Preferences We use cookies to help you navigate efficiently and perform certain functions. 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Save My Preferences Accept All CookiesPowered by Skip to content Home / About Us Meet the People Behind DrugCard Building the Future of Pharmacovigilance Discover who we are, how DrugCard began, and what drives our mission to make pharmacovigilance faster, safer, and smarter. Ask an expert Our History 2019202020212022202320242025 2019 — The idea for DrugCard was born. Brothers Artem and Dmytro Horilyk discussed ways to improve pharmacovigilance processes. At the time, Artem worked as a pharmacovigilance specialist, and Dmytro questioned why literature screening was still performed manually. Their friend Myroslav proposed developing code to automate the process. 2020 — The first version of the system was created. By August, the team completed the MVP and started reaching out to potential clients. 2021 — The first clients and investments. The company signed its first client in April, followed shortly by one of the largest pharmaceutical companies in the region. In December, DrugCard received its first investments from Spain and Ukraine. 2022 — Expansion to Europe and the UK, multinational partnerships. The first European clients joined from Germany, and the team began monitoring new countries. 2023 — AI research and PV services. The team started training AI models on real pharmacovigilance data and launched a PV service (1 specialist, 1 project, 1 country). By year-end: 10 clients, 30 countries, 10 team members. 2024 — LLM model and AI Case Intake. Our AI was first presented in Brussels at the DIA conference The company introduced an LLM model for article categorization and global literature coverage. In December, the AI Case Intake module was released, automatically extracting adverse reaction data from unstructured text. By year-end: 22 team members, 48 clients, 55 countries covered. 2025 — Global scale. DrugCard now operates in 121+ countries, processes over 1 million articles, and provides AI-based global assessment, regulatory intelligence, and safety database solutions. PV services: 3 specialists, 11 projects, and 21 countries. Have questions for our experts? Ask us about pharmacovigilance automation, literature screening or DrugCard platform features. Book 15 minute meeting Contact Us Our mission We create artificial intelligence that performs pharmacovigilance. DrugCard turns data chaos into actionable insights, automates article analysis and reporting, and ensures quality control — so experts can focus on strategic decisions and patient safety. Our Vision We are shaping a new era in pharmacovigilance — the era of autonomous AI specialists. We see a future where AI leads pharmacovigilance processes, and people make decisions based on clear data and predictive insights. DrugCard sets the standard for how AI transforms compliance, safety, and efficiency across the pharmaceutical industry. Our Management Team Artem Horilyk Chief Product Officer Leads product strategy and development, translating pharmacovigilance requirements, automation, and AI into practical customer solutions. Dmytro Horilyk Chief Executive Officer Defines the company’s strategic direction, oversees business operations, and drives DrugCard’s growth across international markets. Myroslav Demchun Chief Technology Officer Oversees the technology strategy and platform development, ensuring scalability, reliability, and security of all solutions. Our Pharmacovigilance Team Olha Lysiuk Head of Pharmacovigilance Leads pharmacovigilance operations, ensuring regulatory compliance and continuous safety monitoring. Yuliia Kuplovska Pharmacovigilance Specialist Conducts local and global literature monitoring, safety data assessment, ICSR preparation, and supports PV audits and SOP development. Sofiia Shunkina Pharmacovigilance Specialist Combines pharmacovigilance and quality expertise with academic work in pharmacy and medical education. Yana Komarnyk PV Specialist, Product Operations & Support Assistant Works with the product and client requests, oversees automated resource screening, and manages service-based PV projects. Yuliia Turok PV Specialist, Product Operations & Support Assistant Manages pharmacovigilance projects, handles support requests, performs local monitoring, and maintains user documentation. Our Sales Team Khrystyna Kiselova Head of Sales & Partnerships Leads business growth, partnerships, and sales activities while managing account and lead management teams. Rostyslav Siarkevych Business Development Executive Works with existing clients, drives upsell and cross-sell initiatives, and manages contracts and billing processes. Viktoriia Horkavenko Lead Generation Manager Identifies and engages potential clients, initiates outreach, and builds long-term, trust-based partnerships. We believe AI will redefine how pharmacovigilance works — and we’re proud to be shaping that future. Explore our solutions Menu Request a demo Name* Surname* E-mail* Phone number* Company* This site is protected by reCAPTCHA and the Google Privacy Policy and Terms of Service apply. Send Book 15 minutes meeting Name* Surname* E-mail* Phone number* Company* This site is protected by reCAPTCHA and the Google Privacy Policy and Terms of Service apply. Book ↑ --- We value your privacyBy clicking “Accept All Cookies”, you agree to the storing of cookies on your device to enhance site navigation, analyze site usage, and assist in our marketing efforts.Cookies Settings Accept All Cookies Customize Consent Preferences We use cookies to help you navigate efficiently and perform certain functions. 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Save My Preferences Accept All CookiesPowered by Skip to content Home / Why DrugCard? Why DrugCard? It’s time to solve your local literature screening gap Entrust your pharmacovigilance routine to us Request a Demo The local literature screening gap Common challenges for drug safety specialists Local sources managment Identifying relevant local journals Checking updates for huge number of issues Managing paid subscription and paper journals Local literature screening Documenting and materials storage Generating weekly reports Article translation from local language Identifying drug safety information Manual reading of journals Time-consuming process Hight possibility of human error Low quality of keyword search in PDF files Ensuring pharmacovigilance compliance Process assessment Continuous tracking of published issues Periodic reconciliation with publishers Quality control process Drug safety teams need an automated local literature screening solution In this new era of automation drug safety specialists frequently work remotely, the number of products increases, and staff need to perform more efficiently. Pharmaceutical companies need a solution that guides teams in real-time through every step of the literature screening, so they can close the gap and work at their full potential. 1. DrugCard addresses the root causes of the Literature Screening Gap and drives a predictable, efficient MLM process for pharmaceutical companies. 2. DrugCard is the first and only Literature Monitoring Platform that automates local literature screening and turns intelligence into actions, from monitoring to management and reporting. 3. When drug safety teams work at their full potential, they achieve more goals with less effort and deliver a better value for patient safety. Automated literature screening Free up to 70% of time spent on this process DrugCard boosts drug safety specialists' productivity by automating literature monitoring, freeing them to focus on other critical tasks with greater efficiency. Traceable workflow Managing MLM with confidence DrugCard gives PV operations leaders real-time analysis of performing MLM process. The PV team can identify more drug safety information, reveal new safety signals and proactively evaluate the risk of the adverse reactions. Digital records in one place Make decisions instead of copypasting data DrugCard centralizes your digital records, guaranteeing that your crucial data is attributable, legible, original, enduring, and accurate. Say goodbye to Excel spreadsheets in 2025! Does this sound like a solution that could help your team right now? We invite you to experience the benefits of DrugCard with a free 2-week trial. Book 15 minute meeting Contact Us Menu Request a demo Name* Surname* E-mail* Phone number* Company* This site is protected by reCAPTCHA and the Google Privacy Policy and Terms of Service apply. 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Save My Preferences Accept All CookiesPowered by Skip to content Home / Implementation & Onboarding Implementation & Onboarding How We Help You Implement DrugCard We support your team at every step of implementing DrugCard - from initial introduction and setup to day-to-day use and ongoing support. This structured approach ensures compliant adoption, clear user accountability, and confident use of the platform within routine pharmacovigilance workflows. Ask an expert User Scope Definition We begin by defining which users and teams will work with the platform. This includes clarifying roles, responsibilities, and access levels to ensure the system is aligned with your internal PV structure and workflows. Initial Training by PV Experts Our pharmacovigilance team delivers an introductory training session for your users. The training focuses on practical use of the platform within real PV processes, ensuring that users understand both functionality and regulatory context from the start. User Account Setup and GxP Traceability We create individual user accounts for all platform users. Each user receives personal access credentials, ensuring full traceability of actions in line with GxP requirements. This approach supports audit readiness and clear accountability within the system. User Manual and Continuous Guidance We provide a detailed User Manual explaining how to work with DrugCard. The manual is available directly on the platform, is accessible to all users, and is updated on a monthly basis to reflect functional improvements and process updates. SOP Template Support To support procedural alignment, we provide a ready-to-use SOP template, such as “Literature Monitoring with DrugCard.” The template includes embedded DrugCard workflows and a clear description of pharmacovigilance processes performed using the platform. Customers may use this document as a baseline and adapt it to their internal quality system. PSMF Annex D and Validation Documentation We provide a dedicated template for updates to Annex D of the PSMF (Computerised Systems and Databases). DrugCard operates within a structured validation framework, and all users have access to current and continuously updated validation documentation. These documents are available directly on the platform, supporting inspection readiness and compliance requirements. Post-Implementation Review and Optimisation After users have started working with the platform, we can perform a review of usage upon request. This includes checking whether the functionality is used correctly, whether key features are applied as intended, and whether search strategies and keywords are optimised. Based on this review, we provide practical recommendations to improve efficiency and monitoring quality. Change Communication and Updates Any platform updates or changes are communicated promptly. We provide clear and concise instructions to ensure users can quickly understand and apply updates without disrupting routine PV activities. Support Availability and Responsiveness Our support team is readily available to assist users when needed. We focus on fast response times and practical guidance to ensure uninterrupted and confident use of the platform. Have questions for our experts? Ask us about pharmacovigilance automation, literature screening or DrugCard platform features. Book 15 minute meeting Contact Us Menu Request a demo Name* Surname* E-mail* Phone number* Company* This site is protected by reCAPTCHA and the Google Privacy Policy and Terms of Service apply. Send Book 15 minutes meeting Name* Surname* E-mail* Phone number* Company* This site is protected by reCAPTCHA and the Google Privacy Policy and Terms of Service apply. Book ↑