Adding EBR allows users to review and address exceptions during the manufacturing process. Exceptions can then be addressed in as they occur, reducing wasted time, money and materials.
Furthermore, quality personnel can investigate process deviations as they occur instead of waiting for batch completion.
“For years, EBR has been interpreted as putting the old paper system behind computer screens; however, computer-based systems are capable of much more”, said Martin Dittmer, FactoryTalk Pharma Suite product manager at Rockwell.
