Regulators such as the US FDA, TGA, HSA, NPRA and MHRA require proof of proper handling for every step of the production process of a Pharmaceutical or Medical Device. Batch records and other types of manufacturing documentation demonstrate this level of accountability. Many companies still use paper-based systems, which are cumbersome and error-prone. The right electronic batch record (EBR) software system removes the documentation burden from quality and manufacturing teams.
To learn more about MasterControl's software systems, please contact a SeerPharma representative.
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