Avista Pharma has over 3,000 square feet of stability areas that include over 25 environmental chambers for pharmaceutical stability studies across three (3) locations. We can accommodate studies of various container and lot sizes, temperatures, humidities, lights and lengths of study. With fully-compliant GMP analytical chemistry and microbiological labs, Avista Pharma is your one-stop stability testing partner with redundant storage locations for business continuity.
Avista Pharma utilizes a LIMS system to support these studies. The LIMS stability module allows for seamless integration of analytical method data with the study management data (pull dates, container quantities, storage locations, upcoming sample pull schedule, etc.). Samples are also individually bar coded and tracked throughout the study life cycle.
For more information, please see our Stability Studies section under Drug Product R&D.