CCIT for Cryogenically-Stored Products 

Some drug products must be stored at cryogenic temperatures, which means temperatures below -150 degrees Celsius. These are typically biologics, such as stem cells and vaccines, which are extremely sensitive to temperature fluctuations. Cryogenic storage is the most effective way to maintain the stability and efficacy of these products. Cryogenic storage involves using liquid nitrogen or other cryogenic gases to support the extremely low temperatures required for these products. Specialized containers and equipment ensure that the products remain at the appropriate temperature during storage and transport. Proper storage and handling of these products are critical to maintaining their potency and ensuring patient safety. 

Gateway Analytical - Analysis Solutions

CCIT Study: Cryogenically-Stored Products

Gateway Analytical is your go-to laboratory for CCIT of drug products stored at extremely low temperatures. Several regulatory agencies have reviewed our validated methods, and will work for your needs. Contact Gateway Analytical today to learn more about our approach to CCIT for storing cryogenically stored products. We recognize that CCIT at cryogenic temperatures demands unparalleled precision, considering the potential for package deformation and seal failure due to extreme cold. It is generally known that CCIT at extremely low temperatures can be challenging due to the potential for package deformation and seal failure caused by thermal contraction of the packaging materials.

Deep Cold, Deeper Expertise.

 Pharmaceutical and biotechnology companies must work closely with regulatory agencies and testing laboratories to develop and validate appropriate CCIT methods for their product-package configurations, including those stored at extremely low temperatures. Contact us today to discover how we can support your cryogenic CCIT needs with our validated and trusted methods.

Gateway Analytical - Analysis Solutions

Early-Phase Development

Comprehensive packages designed to navigate clinical & regulatory complexities of parenteral product-package and container-closure development, from concept to market readiness.

Container Closure
Integrity Testing

Quantitative, non-destructive, deterministic leak detection technologies for products stored in vials, syringes, cartridges, flexible containers, and bottles.

Particulate
Analysis

Multi-analytical methods to count, size, and characterize visible and subvisible particulate matter in pharmaceuticals, disposable containers, single-use systems, raw materials, and medical devices.

Medical Device
Analysis

Rigorous studies focused on enumerating particulate matter and identifying potential chemical compounds that could migrate from medical devices into the environment or directly impact patient health.

Extractables
& Leachables

Studies aimed at identifying potentially harmful compounds in manufacturing components and final containers to ensure the safety and efficacy of pharmaceutical products.