Pharmacovigilance
We work every day to ensure the quality, efficacy, and safety of our medicines.
Pharmacovigilance activities are an essential part of our commitment to health and to the continuous improvement of our products.
The World Health Organization (WHO) defines pharmacovigilance as the science dedicated to the collection, monitoring, investigation, and evaluation of information related to the safety of medicines, with the purpose of promoting their responsible use and protecting patients.
Our Commitment
We receive and document
all information related to adverse events or suspected safety issues associated with a medicine.
We continuously monitor
the effects of our products, biological medicines, and specialty therapies, ensuring ongoing supervision of their real-world performance.
We analyze and assess
each reported case to determine its origin, severity, and frequency, applying internationally recognized scientific and regulatory criteria.
We take action
by implementing corrective and preventive measures that strengthen the safety of our medicines and continuously improve our processes.
For EleaExeltis, pharmacovigilance is not only a regulatory obligation—it is an expression of our commitment to safety, science, and life.
Reporting an adverse event or safety concern
We have an active pharmacovigilance system for the reporting, follow-up, and evaluation of potential adverse events.
If you wish to report a case or a concern related to the safety of a medicine, you may contact our team by completing the form below.
All information provided is confidential and protected in accordance with Personal Data Protection laws and applicable pharmacovigilance regulations.
Beginning of form
Reporting an adverse event or safety concern
We have an active pharmacovigilance system for the reporting, follow-up, and evaluation of potential adverse events.
If you wish to report a case or a concern related to the safety of a medicine, you may contact our team by completing the form below.
All information provided is confidential and protected in accordance with Personal Data Protection laws and applicable pharmacovigilance regulations.
Beginning of form
Certifications and standards
We comply with the highest international quality standards, operating under GMP (Good Manufacturing Practices) and GLP (Good Laboratory Practices), ensuring the safety and effectiveness of all our processes.
