Wolter Somer

Wolter Somer possesses extensive experience in regulatory affairs, having held managerial roles at various organizations. At Vitalize Products since June 2015, Wolter has focused on developing Product Master Files for dietary supplements. Previous roles include Manager Regulatory Affairs at Solipharma b.v. from February 2004 to December 2013, where Wolter was responsible for preparing and submitting complete registration dossiers in ECTD format, and at Regenboog Apotheek, where the management included the full registration dossier for Methadon. Earlier experience at Solipharma bv included the establishment of HACCP and GMP systems as QA Manager from February 2003 to December 2010. Wolter's career began at Circa Dia with the development of a Melatonin dossier. Wolter holds a Bachelor of Science in Analytische chemie/Technisch Chemisch from HTS Chemische Technologie and a Bachelor of Science in Chemische Analyses from HTS Chemie.