About
Veterinary Signal Detection
Signal detection in veterinary medicine is a critical process aimed at identifying potential safety concerns related to the use of veterinary products.
In this training you will learn about the legislative background of the veterinary signal detection process, specific requirements and details about the methodologies for signal detection and signal evaluation (retrieval of EVVET data from the system, statistical signal detection, evaluation methods), as well as about submissions of annual statements.
By the end of the course, attendees will have the knowledge and skills to contribute to the continuous improvement of animal health and safety through robust pharmacovigilance practices.
Programme
The course will address the following topics:
- Legislative background
- What is signal detection
- New requirements in Regulation (EU) 2019/6
- Methodology of signal detection
- EVVET data Warehouse
- Statistical signal detection: concepts of ROR (Reporting Odd Ratio) and SDR (Signals of Disproportionate Reporting)
Regulatory and pharmacovigilance specialists interested in veterinary pharmacovigilance.
Participant experience
No experience is required to follow the course.
Presentation with case studies and interactive Q&A sessions.
Lecturers
Veronika Rucigaj, DVM, PhD
Dr. Rucigaj is a Medical Advisor with over 20 years of experience in the pharmaceutical industry. She holds a Master’s degree in Veterinary Medicine and a PhD in Biomedicine. At Billev Pharma East, she is a key member of the medical team, contributing to the preparation and critical review of high-quality medical and technical documentation for both national and international registrations of medicinal products. She provides scientific and medical expertise to support regulatory submissions in compliance with EMA and local regulatory requirements. Dr. Rucigaj’s professional activities cover both human and veterinary medicinal areas, with additional focus on pharmacovigilance and signal detection. She ensures scientific and medical accuracy in responses to health authority queries and actively supports safety evaluation processes. She continuously maintains up-to-date knowledge of therapeutic areas, clinical guidelines, and evolving regulatory frameworks to promote the safe and effective use of medicines.
Barbara Pavlin, DVM
Barbara Pavlin, DVM is a veterinarian with experience in pharmacovigilance and regulatory affairs for both veterinary and human medicines. She currently works at Billev Pharma East, where she manages pharmacovigilance systems, prepares risk and benefit reports, ensures compliance with EU and UK regulations, and coordinates communication with authorities. Previously, she worked at the Agency for Agricultural Markets and Rural Development of Slovenia, providing technical and audit support for EU-funded projects, and at the Veterinary Station Trebnje, specializing in small animal internal medicine, diagnostics, and treatment. She holds a Doctor of Veterinary Medicine degree from the University of Ljubljana and is fluent in Slovenian and English, with basic knowledge of German. Her skills include pharmacovigilance management, regulatory compliance, communication, and digital literacy.
Online Training – 1 module
22 October 2026 from 2:00 pm to 6:00 pm CEST
Some days before the online training you will receive all details about the connection.
The course will proceed with a minimum number of participants. Should this number not be reached the registered participants will be notified one week prior to the commencement of the course.
Early Bird: € 490,00* (until 01 October 2026)
Ordinary: € 620,00*
Freelance – Individual – Academy – Public Administration: € 390,00*
*for Italian companies: +22% VAT
The fee includes: tuition, organizational office assistance, teaching materials and attendance certificate that will be sent after the training via e-mail.
Register
Printable Version
At the end of the training, you will be able to