Pharmacist Anne Lenaers obtained his
degree in Pharmaceutical sciences from the University of Liège, Belgium in
1992. Between 1992 and 2001 she worked as the titular of an Officine open to
the public in Liège.
Since 2001 she has been working for the
Federal Agency for Medicines and Health Products (FAMHP), which is the
competent authority in Belgium for medicinal products and Health Products
(Medical Devices, Human Body Material and Blood Products) and which is working
as the administration of the Ministry of Health in these matters.
She first worked one year in the
Inspection pillar of the agency and then she moved to the DG pre pillar of the
FAMHP working first 2 years in the division dealing with the Marketing
Authorisation dossiers and since 2004 in the Research & Development
division of the FAMHP.
She was the secretary of the CTFG
workgroup of the Heads of Medicines Agencies from 2008 until 2011 and is responsible
of the CTA initial trials unit in the R&D division since 2013.