Pharmaceutical & Biotech

Verify GMP
execution on the floor.

EASE makes GMP verification simple for quality and operations teams, from the cleanroom to the production floor. Document every check. Route findings to corrective action. Use targeted retraining to fill compliance gaps.

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Document GMP compliance where the work happens.

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Verify the steps that protect the patient
Confirm line clearance, cleaning verification, and environmental controls are done right every shift and every batch.
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Prevent process gaps from becoming deviations
Identify execution drift and skipped steps early, so you can act before they become batch holds or complaints.
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Walk into inspections with defensible verification records
Get a complete, time-stamped record of every check, finding, and corrective action to stay inspection-ready.

Correct process issues before they hit the batch record.

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Keep every check on schedule

Set the frequency for floor-level checks and inspections from your SOPs, then send checklists directly to mobile devices. Schedule an entire year’s worth of audits and inspections with just a few clicks.

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Incorporate visual standards into checklists

Build reference photos and acceptance criteria into every checklist to show your team exactly what a correct material inspection, gowning step, or environmental monitoring sample looks like. When a check fails, the reaction plan shows what to do next to close the loop.

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Close findings before they become CAPAs

Send every finding to a corrective action with a named owner and due date. Overdue items escalate automatically to supervisors, and nothing closes until the fix is verified.

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Track the trends that predict compliance

Watch completion rates and open findings across your sites to spot compliance drift and repeat issues before they show up in a deviation or a 483 observation.

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Manage your audits and inspections in one place

Run GMP audits, safety inspections, and preventive maintenance audits from one system instead of spreadsheets or binders. Produce complete records on demand when a sponsor or regulator asks.

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Hold every site to the same standard

Roll up performance across all facilities or drill down into individual sites or client programs. Give leaders the visibility to track underperforming sites and focus resources where compliance risk is highest.

Capture defensible records of frontline verification activities.

EASE turns quick mobile checks on the production line into documented verification of compliance with key quality and safety requirements.

  • Walk into FDA and EMA inspections with evidence that cGMP steps are consistently followed on the manufacturing floor.
  • Keep workers safe around solvents, high-speed lines, and manual handling processes, with detailed records of hazard mitigation and on-the-job retraining.
  • Document compliance with client-specific and product-specific requirements to streamline sponsor audits.
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Even though we have a no-blame policy, supervisors know we hold them accountable for paying attention to the details. EASE helps us get to the root cause so we can strengthen our team.

Rick Lindquist
EHS and Continuous Improvement Manager at Berry Global