Automated medical literature monitoring

Entrust your routine but important tasks to us, as your drug safety specialists.

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DrugCard - next generation SaaS for pharmacovigilance

Medical literature monitoring

Big database of medical and scientific literature, including local journal sites and publications from EMA, WHO, FDA, MHRA, TGA, PMDA, Swissmedic, and local Health Authorities.


Integration with MedDRA medical dictionary. E2B R2/R3 support. Easy ICSR converting to XML in accordance with international ICH requirements.

Reference drugs monitoring

Automatic comparison of leaflets for medical use of your medicines and reference products. If any changes are detected, you will receive an immediate notification.

Data Integrity

The system complies with FDA CFR 21 Part 11, which sets requirements for electronic records and signatures. We provide a certificate of conformity, so you can officially use the system for EU, US, CIS markets as well.

Information security

We use data centers with a certified information security management system according to ISO / IEC 27001:2013 and DigitalOcean SOC 2 Type II.

24/7 access

Since we provide Software as a Service - you get the full access at any time. We guarantee "invisible" system maintenance.

Medical literature monitoring with AI technologies

The only SaaS on the market that allows automated medical literature monitoring in any language, not limited to websites and also within:

  • Any PDF files (even scanned)
  • DOC \ DOCX files
  • Images

No need to download and read files yourself now. The system will do it for you.

Request a Demo

Request a Demo DrugCard and get free access for two weeks. Experience the benefits of our system, which is already using by leading companies

  • Automated local medical literature monitoring
  • Reference drugs monitoring
  • Get info even from scanned files
  • Modern database of ICSRs
  • MedDRA support and full regulatory compliance
Dmytro Horilyk

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Our Team

Artem Horilyk
Chief Product Officer
Dmytro Horilyk
Chief Executive Officer
Myroslav Demchun
Chief Technology Officer

Full compliance with GVP and GMP

The system contains built-in support for the necessary functions to ensure GxP activity and good documentation practice. At your service:

  • User access roles control
  • Audit trail
  • Literature monitoring log
  • Articles workflow

Data integrity requirements are met in accordance with the GAMP5 Guide: Records & Data Integrity and CFR 21 Part 11.

How does it work?

Working with DrugCard electronic pharmacovigilance platform for literature monitoring is as easy as 1-2-3

Add your drug

Create a drug's card to start medical literature monitoring

Add keywords

Add keywords, such as trade name, substance or excipients

Get your results

Review the results. Receive periodic updates about new articles found

DrugCard works more. Costs less. It's simple

A weekly manual medical literature monitoring among 20 sources on 40 drugs is 40 hours a week of work (1 rate of the specialist in pharmacovigilance).