QPPV & Deputy
Comprehensive support for the Qualified Person for Pharmacovigilance: role assumption, regulatory responsibilities and interface with regulatory authorities.
GVP Compliant
EMA Guidelines
Partner Istituzionali & Congressi Internazionali
Our Services
Complete Pharmacovigilance Solutions
A multidisciplinary team of experts at your disposal for every aspect of drug safety management.
PSMF Management
Drafting and maintenance of the Pharmacovigilance System Master File in compliance with GVP modules, with continuous updates and audit trail management.
EudraVigilance
Complete management of XEVMPD data entry, ICSRs submission, reconciliation and reporting to EMA with maximum accuracy and timeliness.
Literature Monitoring
Systematic global and local screening of scientific journals and medical databases to identify emerging safety signals and update the risk profile.
PSUR & RMP
Professional drafting of Periodic Safety Update Reports and Risk Management Plans according to the latest EMA templates and international regulatory requirements.
Audits & Training
Regulatory compliance audits, mock inspections, and customized training programs for your team on GVP, ICH E2E and industry best practices.
Excellence is Made of People
A Team of Experts by your side.
Our strength lies in multidisciplinarity. The Eureka InfoMed team is composed of professionals with years of experience in pharmacovigilance, regulatory affairs, and scientific research, ready to ensure maximum precision for all your MA needs.
20+
Years of experience
12
Dedicated professionals
100%
Guaranteed compliance
Why Choose Us
The Partner that makes the difference
Entrusting pharmacovigilance to Eureka InfoMed means choosing safety, competence and operational peace of mind.
100%
Regulatory compliance
Scientific Precision
Our multidisciplinary team integrates physicians, pharmacists, regulatory experts and scientists with deep pharmacovigilance specialization, ensuring rigorous analysis and impeccable documentation.
1:1
Guaranteed direct access
Direct Access to Decision-Makers
Our lean structure guarantees you direct access to project managers and an operational flexibility that large organizations cannot offer.
20+
Years of experience
Zero Organizational Stress
We handle deadlines, GVP updates, EMA notifications and AIFA communications. You focus on your business: organizational management is in expert hands.
Ready to discover how to optimize your pharmacovigilance processes?
Talk to one of our experts today. Free consultation, no commitment.
Contact Us
Request a Free Consultation
Fill out the form and one of our experts will contact you within 24 hours.