Audiment vs MasterControl Quality Excellence

Built for physical frontline store inspections: kitchen hygiene, refrigerator temperatures, visual merchandising, service speed, and cashier protocols across distributed commercial locations.

Built for FDA-regulated pharmaceutical and medical manufacturing: electronic batch records (EBR), cleanroom deviation tracking, and GxP document control.

Used by frontline shift supervisors, store managers, and regional coaches on personal smartphones (BYOD) walking physical store aisles.

Used by pharmaceutical cleanroom technicians, QA compliance directors, and regulatory affairs executives working on validated manufacturing terminals.

Photo evidence is captured strictly through an in-app live camera modal with front/rear flip and orientation correction. Device gallery uploads are restricted by default, preventing staff from submitting pre-saved or stock photos.

Evidence collection centers on validated electronic signatures, digital batch records, cleanroom environmental monitoring sensors, and laboratory test data.

Enforces high-accuracy GPS geolocation capture directly at final submission. If coordinates cannot be verified on-site within an 8-second window, submission is strictly blocked until physical presence is confirmed.

Operates inside controlled pharmaceutical manufacturing facilities; physical presence verification and GPS geofencing are completely irrelevant to cleanroom batch records.

Critical store failures automatically generate a tracked CAPA document with a strict 48-hour SLA assigned to the store manager, backed by proactive 6-hour cron reminders and photo-verified closure.

Manufacturing deviations trigger formal FDA-regulated CAPA investigations involving multi-week laboratory testing and regulatory filings.

Supports surprise audits (suppressing manager pre-notifications) and 'Flashmob' mass-dispatches with custom hourly deadlines to verify promotional rollouts or sudden operational issues across all stores.

Audits are formal FDA regulatory inspections or supplier audits scheduled months in advance.

Dashboards provide cross-branch benchmark rankings, regional performance trends, and automated trend alert banners (flagging locations that score below threshold on 3+ consecutive audits) to surface systemic drift instantly.

Dashboards visualize cleanroom batch release yields, open deviation cycle times, and regulatory audit readiness.

Flat per-location pricing with unlimited users per branch. Shift managers, assistant store leads, head chefs, and regional coaches all have dedicated accounts without driving up monthly software licensing bills.

Enterprise life sciences software pricing based on licensed cleanroom seats, plant sites, and validated modules, running into tens of thousands of dollars.

100% cloud-and-mobile responsive web app/PWA. Runs on any smartphone browser instantly via web link without requiring App Store downloads, MDM provisioning, or personal storage consumption.

Validated desktop enterprise web portal requiring formal Computer System Validation (CSV) under FDA regulations.

Audits continue fully offline without interruption. You can capture live camera photos, complete logic-based checks, and the system syncs automatically in the background once the device reconnects to Wi-Fi or cellular.

Requires validated corporate cloud connectivity for real-time electronic batch record updates.

Built for store floors, not pharmaceutical cleanrooms

MasterControl is built for cleanroom technicians managing FDA electronic batch records. Audiment is built for operations teams inspecting store floors, kitchen hygiene, and brand standards on smartphones.

48-hour automated CAPA SLAs

Store operational defects cannot wait for multi-week clinical investigations. Audiment automatically triggers 48-hour SLA tasks with photo verification to fix store issues immediately.

1-2 week deployment vs multi-month software validation

Audiment deploys across store branches in days without requiring FDA Part 11 computer system validation (CSV).

FDA-regulated pharmaceutical and medical device manufacturing

If you operate a pharmaceutical cleanroom, biotechnology production facility, or medical device plant requiring validated electronic batch records (EBR) and FDA 21 CFR Part 11 compliance, MasterControl is an industry-leading life sciences eQMS.