Shelf-Life Evaluation for Medical Devices, Device Materials, and Sterile Barrier Systems
Medical devices and packaging materials may change over time. Accelerated aging studies help evaluate how these changes may affect critical properties related to product safety, performance, and packaging integrity within a shorter period.
Studies planned in accordance with ASTM F1980 can be applied to sterile barrier systems and their packaging materials, as well as medical devices and device materials for which the method is suitable.
Aging conditions and post-aging evaluations are defined based on the product characteristics and intended shelf life.
Let's Define the Right Aging Plan for Your Product
We help you determine the appropriate study scope based on your target shelf life, product materials, packaging design, and storage conditions.
To discuss accelerated aging protocol development and related testing, please complete this request form and send it to info@nioreg.com.
