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MAXLife Electronic Batch Records
Many Life Sciences manufacturers today rely on paper-based and
people-intensive processes to document every step in the
production process of a batch to comply with GMP and other
compliance standards. There are many disadvantages to this
approach of managing batch records:
Paper-based processes increase
operating costs, risk, and the possibility of human errors.
Manual batch operations are
inefficient, time-consuming, and slow time to market.
Physically managing batch records is
complex and provides limited tracking and visibility in the
event of any non-conformances.
MAXLife provides Electronic Batch Record (EBR) capabilities that
reduce manual processing and operating costs by tracking Batch
Records electronically, having them go through a life cycle of
approvals, security, and workflows along the way.
Benefits of the MAXLife Electronic Batch Records (EBRs):
Complete document lifecycle
management capabilities, including automated workflows, audit trails,
and full versioning support.
Reduces time, effort, and costs
associated with manual and paper-based processes.
Enables compliance with industry and
government regulations (including FDA 21 CFR Part 11).
Increases traceability and enforces
document / data security.
Integrated quality control and product safety document management solution for Recalls, CAPA, SOPs, Audits, Complaints, GMPs and more!
MAXLife Electronic Batch Records (EBR) eliminates costly
paperwork errors, speeds up information distribution and
collaboration, and enables strategies for improving quality and
efficiency. MAXLife makes it easier for Life Sciences companies
to access and track batch records, model and change complex
processes, and speed time-to-market.
MAXLife ERP can dramatically improve profitability, productivity, and product safety at even the most complex organizations.
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