Electronic Batch Records (EBRs) are a form of digitized compliance. They help to reduce errors, streamline traceability, and generate a low volume of documents in the Life Sciences space.
The EMA and FDA Current Good Manufacturing Practices (CGMPs) require proof of proper handling for every step of the production process. Batch records and other types of manufacturing documentation demonstrate this level of accountability. Paper-based systems are cumbersome and error-prone. The right electronic batch record (EBR) software system removes the documentation burden from quality and manufacturing teams. It also improves product quality and key performance metrics.
Promeridian can ensure compliance and improve efficiency by automating your paper-based systems with an integrated EBR system.
