Compliance-ready maintenance for life science teams
Pharmaceutical and biotech manufacturers use eMaint to reduce audit prep time, eliminate compliance gaps, and extend asset life — without disrupting validated environments.
We help customers be 21 CFR Part 11 compliant.
Download the white paper
How risk-based validation and
continuous process verification
give life sciences teams a
competitive edge.
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.
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: from 50% to 9 0% + PM compliance across all sites
90%+
Cumplimiento PM
21 CFR
Part 11 validated
Multi-site
standardized
