Data Sheet
Batch manufacturing records help manufacturers show compliance with Current Good Manufacturing Practices (cGMP) outlined by regulatory authorities. Electronic batch record (EBR) systems offer a high level of control and visibility in real time that paper-based systems cannot. Improve your efficiency by automating shop floor processes and ensuring complete, accurate records. Learn more about MasterControl EBR software in this data sheet.
MasterControl Manufacturing Excellence helps companies around the world automate their batch record processes to meet regulatory requirements.
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cGMPs require extensive EBR systems documentation. This includes the following: Batch dates Identity of major equipment/lines used Components/materials used and their weights and measures In-process and laboratory control results Complete labeling control records Sampling Identification of personnel supervising or checking each step
Pharmaceutical companies have traditionally used paper (hard copy) to maintain production batch records. With the advent of 21 CFR Part 11 in 1997, the FDA began to accept EBR systems like MasterControl Manufacturing Excellence. When you adopt an EBR software system, it must be in compliance with regulations found in 21 CFR Parts 210-211.The requirements include a time-stamped audit trail, reporting, electronic signature and security requirements.
EBR software prevents mistakes from slowing the entire production process.
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