From raw material identification to finished and packaged pharmaceutical products, drug stability testing is a critical step for both research and development (R&D) and quality control (QC), with a tremendous impact on customer safety. Stability chambers are enclosures used to test the “stability profile” of a drug — documentation on how the quality of a drug may vary over time under the influence of a variety of parameters. Temperature and humidity are key factors controlled when using stability chambers.

Maximizing control over the stability testing process allows pharmaceutical manufacturers to obtain the most thorough, accurate results as efficiently as possible—avoiding any number of issues that can negatively influence the efficacy of testing results and/or the quality of products produced.