Our Stability Studies are designed to evaluate the shelf-life, storage conditions, and long-term quality of pharmaceutical products, ensuring compliance with global regulatory standards (such as ICH, FDA, and EMA guidelines).

We conduct a range of stability testing protocols to assess:

• Physical, chemical, and microbiological stability
• Degradation pathways and impurity profiling
• Temperature, humidity, and light exposure impacts
• Container/closure system integrity

Our team provides data to support regulatory submissions, product labeling, and formulation optimization, ensuring your product maintains its efficacy, safety, and quality throughout its intended shelf life.

With state-of-the-art stability chambers and rigorous testing methodologies, we deliver reliable, reproducible, and accurate results, empowering you to meet regulatory requirements and market demands.