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
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.
Secant Group:
from 50% to 9 0% + PM compliance across all sites
See eMaint in a validated environment
30-minute demo tailored to life sciences use cases. No generic product tour.