Documentation / Turnover Packages
D ocumentation is critical to comply with Current Good Manufacturing Practice (cGMP) regulations, which require proof the manufacturing process repeatedly generates pharmaceutical products that meet attributes relating to identity, strength, quality, purity and potency. Sani-Matic's turnover packages are extremely detailed and designed to minimize your validation costs. A dedicated team of documentation specialists ensures you have the documentation required to validate your cleaning process. Detailed Turnover Packages to Meet Bio-Pharm Validation Requirements
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