In 2017 piCHEM opened a brand new production facility providing 1.200m² edge-cutting laboratory and production space as well as adequate storage rooms. Peptides are manufactured in compliance with ICH guidelines and according to applicable laws and regulations. The production facilities are inspected and approved by the national authorities, the US FDA and the japanese PMDA.
Our pharmaceutical contract manufacturing department supports your drug development project through all stages of clinical trials. piCHEM conducts GMP manufacturing of APIs from milligram to several hundred gram scale.
piCHEM offers peptide synthesis according to GMP with applicable techniques in peptide chemistry. Depending on the structure, quantity or special client requirements, different strategies are available, from conventional synthesis in solution to solid phase synthesis methods (SPPS).
Reversed phase chromatography and ion exchange chromatography are applied as standard purification procedures for synthetic peptides.
Peptides are available as lyophilisate in bulk or in bulk aliquots. For final manufacturing steps, cleanrooms in class D/C are available.