Compare CDMOs with ICH stability testing capabilities. Filter by chamber capacity, ICH condition support, and regulatory filing experience.
15 companies listed
Stability testing determines how a drug product changes over time under defined storage conditions (temperature, humidity, light). ICH guidelines (Q1A-Q1E) specify the conditions, timepoints, and statistical analysis methods used globally. Stability data is required for regulatory submissions to establish shelf life and storage conditions.
CDMOs offering stability services need: validated stability chambers (temperature and humidity controlled), GMP-compliant analytical testing capabilities, sample management systems for multi-year programs, and regulatory expertise to design study protocols that support global filing strategies.
France
Analytical and toxicological expertise at your service A comprehensive offer for your health products Supporting you from designing to marketing your product is our priority. Staffed with 100 employees, whose sole goal is to ensure your projects are successful. 2 sites in France: one site specializing in NMR based in the Paris area, and our primary site based in Provence. The combination of our analytical capacity and our consulting department is a major asset to meet your needs in terms of development, process validation and quality control. We also intervene upstream, providing bespoke support during your R&D phases.
United Kingdom
Cormica has a proud heritage spanning over six decades, partnering with pharmaceutical, medical device, and combination product manufacturers to accelerate safe, compliant product development and release. From R&D to post-market surveillance , we deliver end-to-end testing solutions across analytical chemistry, microbiology, and physical testing. Our GMP, GLP, and ISO 17025 accredited laboratories across the world ensure global regulatory technical excellence.
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