At Ceyone Life Sciences, stability studies are a vital part of ensuring the quality, safety, and shelf-life of pharmaceutical products. Our comprehensive testing programs evaluate how environmental and stress factors influence the efficacy, purity, and integrity of drug substances and products over time. These studies generate critical data for regulatory submissions and play a key role in guiding formulation development and storage conditions.
- Real-Time Stability Studies
Long-term monitoring of product performance under recommended storage conditions.
- Accelerated Stability Studies
Evaluations under elevated conditions to predict long-term stability and establish shelf life.
- Purification & Isolation
Preparing pure compounds via prep-HPLC (normal & reverse phase), lyophilization, crystallization, and other isolation techniques to prepare standards, intermediates, or batch materials.
- Stress Studies
Determining degradation pathways under extreme conditions such as heat, humidity, oxidation, and pH variations.
Why Choose Ceyone?
State-of-the-art stability chambers with controlled temperature and humidity settings.
Analytical support with advanced instrumentation for accurate characterization.
Data aligned with global regulatory guidelines (ICH, USFDA, EMA, WHO).
Reliable reports for regulatory filings, shelf-life determination, and formulation optimization.