Pharmaceutical businesses are pushing for the computerization of manufacturing processes and documents, which is not only precise and transparent in terms of decentralization, data, and recording time, but also convenient for reviewing.
As a result, evaluating and implementing a computerized system or software to manage all types of records and documents is critical in order to meet the GxP criteria. To gain a deeper understanding of this topic, SEN Pharma partnered with Factorytalk, which has more than 18 years of experience in MES, EBR, eQMS, and CSV for GxP activities in the pharmaceutical industry, to co-host this Webinar “Ensuring Data Integrity with CSV and GxP compliant software”.
Facebook: SEN Pharma – Boosting Pharma Industry
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