Our mission is to provide the best possible service.
Our vision is to make a difference.

The pharmaceutical Industry is one of the most highly regulated industries in the world.
During recent years, numerous changes in European medicines legislation and guidelines have even increased the scope and regulatory impact
of pharmacovigilance activities, requiring an ever greater interaction between the areas of pharmacovigilance and regulatory affairs.

Despite international efforts towards harmonisation of requirements, regulations laid down by different governments and their interpretation
by the Health Agencies still do not always match. As a result, registration data prepared for one country frequently fail to meet the requirements
in another country.
Pharmaceutical Companies have to find the means and knowledge to comply with these ever-changing challenges.

Vetmedico bvba is the missing link between both areas, providing expert advice and support in a custom-made setting.

eXtended EudraVigilance Medicinal Product Dictionary (XEVMPD): Electronic submission of information on medicines
(following the new pharmacovigilance registration Art. 57, Regulation (EC) No. 726/2004. Are you fully compliant yet?

Contact us for more info at info@vetmedico.be
Member of Association of Veterinary Consultants - Belgian Regulatory Affaires Society - Vlaamse Dierenartsenvereniging - Orde der Dierenartsen