FDA Establishment Registration
for Testing Laboratories
FEI NUMBER: 3015176596
GOOD MANUFACTURING PRACTICES
AIFA (Italian Medicines Agency) has authorized CHIMAN to perform analytical controls on medicinal products and investigational medicinal products (GMP) since July 2006.
CHIMAN has been admitted to clinical trials of medicinal products according to Italian D.M. 19 March 1998 since August 2007 (AUSL of Piacenza issued the qualification on 03 August 2007, prot. N. 42567).
AIFA (Italian Medicines Agency) on 17 April 2008 (communication N. AIFA.II/40983/P/i.5.i.m/O) has recorded CHIMAN admission to perform laboratory analyses for Phase I / Bioequivalence / Bioavailability Studies from clinical trials of medicinal products on healthy volunteers (according to Italian D.M. 19 March 1998).