Regulatory affairs team is central to Galenix as It coordinates the numerous steps in developing new medical products within an appropriate regulatory framework
With more than 15 years of experience, the Regulatory affairs Department is in charge of the documentation required for registration of drug substances and drug products:
The Regulatory affairs also Coordinates Phase I clinical studies in partnership with more than 10 C.R.O. in Europe and worldwide, bioanalysis and toxicology laboratories.
GALENIX INNOVATIONS - Allee des Palanques - 33127 ST JEAN D'ILLAC - FRANCE
Tel: +33 (0)826 39 69 18 - Fax: +33 (0)5 56 68 83 01