CORDENPHARMA BRUSSELS (BE)
Core Capabilities
- >> Liquid-Phase Peptide Synthesis (LPPS)
- >> Solid-Phase Peptide Synthesis (SPPS)
- >> Rapid peptide synthesis using persilylation technique
- >> Hybrid strategies (SPPS-LPPS)
- >> Complex peptides & peptidomimetics
- >> Cyclic peptides & peptides with multiple disulfide bridges
- >> Short peptides (10-12 residues), often with no HPLC purification
- >> Arginine-rich peptides
- >> Nucleotides, cyclic dinucleotides
- >> Spray drying
CordenPharma 15 Year Anniversary
COMPLIANCE
- >> 7 FDA inspections: Most recently February, 2017
- >> Belgian Health Authorities: Most Recently January 2020
- >> Registered in the EUDRAGMDP database according to EU Directive 62/2011
- >> Relevant GMP Certificates are available on EUDRAGMDP database
- >> The QMS assures compliance to cGMP – as per EU GMP, Part II and ICH Q7
- >> DMF filing experience: USA, Europe, Switzerland, Bosnia and Herzegovina, Japan, Australia, Canada, New Zealand, Singapore, Indonesia, Malaysia, China
Related Products & Platforms
Drug Products
Technology Platforms
Facility Legacy
Founded in 1987, CordenPharma Brussels, formerly Peptisyntha, was a member of the Solvay group until being acquired by CordenPharma in October 2013. CordenPharma Brussels has built a 30 year track record of success in supplying pharmaceutical and biotech companies with clinical and commercial scale cGMP peptide APIs manufactured using world-class cost-effective production processes. Through expertise and capabilities in all synthetic peptide manufacturing technologies, CordenPharma Brussels assesses and customizes their manufacturing approach to achieve the most effective manufacturing process for their customers.
CordenPharma Brussels has developed a portfolio of innovative proprietary technologies with the objective to shorten synthetic processes / reduce the number of processing steps, control quality, and simplify purification steps (or eliminate HPLC purifications for short peptides).
HISTORY
- >> 1987: Peptisyntha founded on the Solvay Campus
- >> 1996: First pre-approval FDA inspection for a major peptide API manufacturer made by Peptisyntha for the worldwide market; Following FDA inspections: 1999, 2005, 2009, 2013, 2015 and 2017
- >> 2001-2008: Production plant extension: new small-scale and large-scale GMP units
- >> 2006-2008: Additional capabilities, further kilo-lab capacity, new QC/microbiology labs, new warehouse
- >> 2011: Solid-phase peptide production units added
- >> October 2013: Peptisyntha acquired by ICIG (International Chemical Investor Group) to join CordenPharma
- >> September 2016: Peptisyntha S.A. name changed to Corden Pharma Brussels S.A.
- >> 2017: EMA Inspection
- >> 2020: Inspection by Belgian Health Authorities
- >> 2022 Astorg acquires CordenPharma from ICIG
Managing Director
Jean-Luc Dewez
Corden Pharma Brussels S.A.
310 rue de Ransbeek
1120 Brussels
Belgium
Phone: +32 2 263 14 11