The Kymos Group is an analytical CRO with three European laboratories devoted to providing bioanalytical and CMC services for the life science industry throughout the entire product life cycle: from early research and development to manufacturing and commercialization. We are GLP- and GMP-certified, have been successfully inspected by the EMA, ANVISA and the FDA and are experts in analytical and quality control work with small molecules, biologics, TIDES (oligonucleotides and peptides) and advanced therapies. Kymos Group provides services to clients worldwide in the pharmaceutical, biotechnology, veterinary, fine chemistry, cosmetic and nutraceutical industries
Service
Method Development, Validation, and Transfer
Kymos has two GMP-certified, EMA and FDA-inspected EU sites fully dedicated to analytical method development and validation for CMC
Service
Kymos Group provides GMP-certified analysis for all raw materials used in the pharmaceutical industry. Both APIs and excipients.
Service
GMP-certified ICH and ongoing stability studies, various climatic zones and 100m3 of EMA and FDA inspected storage capacity.
Service
Pre-clinical & Clinical Bioanalysis · GLP & GCP Compliant
Bioanalysis of Small Molecules & Generics , Bioanalysis & Immunogenicity of Biologics & Biosimilars & Nucleic Acids.