|
Competent
Authorities - R&D with GMO-medicinal products
(Last revised:
January 15, 2007
)

The deliberate
release of GMO in the
environment is forbidden by the federal Law. An advanced authorisation MUST
be
obtained before carrying
on such experiment.
The federal administration is
specifically responsible for the management and follow-up of administrative
procedures. However,
one or more regional administration(s) participate(s)
in the decision process with the federal administration.
Authorisations are delivered on basis
of an advice
of the Biosafety Advisory Council.
COMPETENT
ADMINISTRATION AT THE FEDERAL LEVEL
Federaal Agentschap voor Geneesmiddelen en Gezondheidsproducten (FAGG)/
Agence Fédérale des Médicaments et Produits de Santé (AFMPS)
Eurostation II 8th floor
Place Victor Hortaplein
B-1060 Brussels
Ph.: +32 (0)2 524 80 00
Fax: +32 (0)2524 80 01 |
COMPETENT ADMINISTRATIONS AT THE
REGIONAL
LEVEL
The administration involved depends on the site where the
release of the experimental GMO takes place.
Walloon
Region
Ministère de la Région Wallonne
Direction Générale des Ressources Naturelles et de l'Environnement
(DGRNE)
Division de la Prévention et des Autorisations
Avenue Prince de Liège 15
B-5100 Namur
081 33 61 49
081 33 61 22
DPA.DGRNE@mrw.wallonie.be
http://mrw.wallonie.be/dgrne/dppgss/index.htm
Flemish
Region
Vlaamse Minister van Leefmilieu
Departement Leefmilieu, Natuur en Energie (AMINAL)
Afdeling Milieuvergunningen
Graaf de Ferrarisgebouw
Koning Albert II-laan 20 bus 8
B-1000 Brussels
02 553 79 97
02 553 79 65
Aminal@lin.vlaanderen.be
http://www.mina.be/
Brussels Region
Brussels Institute for Management on the Environment (IBGE-BIM)
Gulledelle 100
B-1200 Brussels
02 775 75 75
02 775 76 21
info@ibgebim.be
http://www.ibgebim.be/
|