In a validated environment the maintenance record is a regulated document. Calibration state, change control, and who performed the work carry the same weight as the work itself — a CMMS that cannot produce defensible records is not usable here regardless of its other features.
Audit trail integrity is the gate. Electronic records need attributable, time-stamped, tamper-evident history — evaluate that before you evaluate anything else, because no amount of usability compensates for a record that won't survive an inspection.
The equipment that shows up in nearly every a pharmaceutical facility.
The plant maintains the air handler, the autoclave, the water skid, the press and the isolator. A validated setpoint is not a maintenance input. Pick this industry at signup and all of it is created for you — no import, no configuration.
PPE:
Hazard zones:
Pick Pharmaceutical & Life Sciences at signup and your plant is standing up in about three minutes — equipment, PMs, quality checklists, and safety inspections included.