50%

reduction in calibration costs
through intelligent automation

85%

reduction in unplanned downtime
for eMaint customers

20–40%

extension of asset life, deferring
capital replacement

Sound familiar?

Audit prep takes weeks, not days

Manual documentation and inconsistent records
across sites make every inspection stressful.

Maintenance data lives in spreadsheets

Fragmented, unvalidated data creates compliance gaps and makes traceability impossible.

Revalidation slows everything down

Every system update triggers a documentation
marathon — delaying technology adoption.

Inconsistent practices across sites

What works at one facility doesn ‘t translate to
others — standardization feels out of reach.

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Built for validated environments

Risk-based validation

Focus validation effor t where it matters most. eMaint helps you tier assets by criticality and maintain documented evidence for inspectors.

Continuous process verification

Improve visibility through downloadable audit trails on each record that update automatically – no manual documentation or paper records needed.

Data governance & integrity

Role-based access, CFR Part 11 compliant audit trails, and a single source of truth for asset data across every site.

Customer Story: Medical — medical device manufacturer

Secant Group needed a CMMS that was 21 CFR Part 11 compliant and fully validatable. After implementing eMaint, they standardized maintenance across all locations — with electronic signatures and timestamped audit trails ready for every inspection.

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Secant Group: 

from 50% to 9 0% + PM compliance across all sites

90%+
PM compliance
21 CFR
Part 11 validated
Multi-site
standardized

See eMaint in a validated environment

30-minute demo tailored to life sciences use cases. No generic product tour.