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Union Product Database.
Supporting all safety aspects of your veterinary products.

What is the Union Product Database?

The Union Product Database functions as the central repository of data concerning approved veterinary medicines and their accessibility across European Union (EU) and European Economic Area (EEA) Member States.

The European Medicines Agency (EMA), in cooperation with the Member States and the European Commission, established and continues to oversee the Union Product Database and the publicly accessible Veterinary Medicines Information website.

Click for information from EMA on the Union Product Database.

How Aeigisana’s Veterinary Pharmacovigilance team can support you?

Flexible options.

Our Veterinary Pharmacovigilance team can manage all of your product/people/safety information updates from our database or yours to keep you fully compliant.

Committed to your success.

We are dedicated to forging a robust and strategic partnership with you throughout the entire lifecycle of your VMP product portfolio.

Your success is our priority, and we are here to ensure it through our comprehensive approach to veterinary pharmacovigilance.

"Professional excellence from a great team highly experienced in different areas of the business such as pharmaceuticals, cosmetics, etc. and with extensive knowledge in the activities offered."
Belén SegarraRegulatory Affairs Head / Technical Director, Qualix Pharma.
"Aegisana not only meets, but exceeds the highest standards in Pharmacovigilance services, which is exactly what we have received. Their commitment to excellence is evident in every aspect of their work."
Alfonso Lomas Pharmacovigilance Activity Coordinator, Mana Pharma.
"Aegisana is an innovative, reliable company with which we have achieved 100% results. I would like to highlight their professionalism, availability, and efficiency, as well as their exceptional communication. We have a close relationship that creates real teamwork."
José Manuel de la Torre GarcíaQualified Person & Regulatory Affairs Manager, Tora Laboratories.
"Moving to Aegisana is a change that Qualix Pharma opted for years ago and they have more than met our expectations."
Belén SegarraRegulatory Affairs Head / Technical Director, Qualix Pharma.
“Aegisana’s technicians are highly trained experts, and their experience is invaluable for all our Pharmaceutical projects."
Alfonso Lomas Pharmacovigilance Activity Coordinator, Mana Pharma.
"We have been working with the team at Aegisana since its inception and it has been a great success. Pharmacovigilance is clearly a passion at Aegisana, and I cannot recommend a better partner to entrust your project requirements to. You are safe in their hands."
Sergio ArroyoLaboratory Director, Netpharmalab Consulting Services.
"In this sector, after years of experience, it is not easy to find a company that offers this type of service at such a high level, involving security, ease of management and communication, and optimization of work for the subcontracting company."
Belén SegarraRegulatory Affairs Head / Technical Director, Qualix Pharma.
“Working with Aegisana is super easy! They adapt to the needs and resources of our company 100%. They helped us update our PV department due to the change in legislation and the experience was fantastic."
Almudena Pradera DVM PhDChief Scientific Officer, EquiCord.
"A team very involved and responsible in every task developed and service provided. Excellent communication with quick advice and response."
Belén SegarraRegulatory Affairs Head / Technical Director, Qualix Pharma.
"The Aegisana team are experts in everything related to pharmacovigilance, giving us confidence and peace of mind. We work with them as a partner as if they were an internal company department."
Marta ManzanaresRegulatory Affairs, Quality Assurance & Pharmacovigilance Manager, Adamed.

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