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The Integration of Stability Testing into Quality Assurance and Compliance Protocols
- Written by: Cantrol Environmental
- Original Recording
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Integrating a stability chamber into a quality management system is a regulatory necessity for any company involved in the life sciences, forming a cornerstone of product development and post-market surveillance. The data generated from these chambers is submitted to health authorities like Health Canada and the FDA to prove that a product remains safe, effective, and of high quality throughout its proposed shelf life under various climatic conditions.
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