Quality Management

Improve quality. Prevent deviations. Standardize excellence.

Manage audits, inspections, observations, CAPAs, and change control in one platform. Glartek's solution is built to help teams meet ISO requirements and reduce repeat issues across sites

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User interface showing a 5S audit dashboard on a tablet with tasks and inspection scores, alongside two mobile screens displaying a checklist and a voice chat for incident reporting.

Your Challenge

Increasing pressure to improve quality and reduce non-conformities

Quality teams are expected to prevent issues before they happen. However, they are expected to deal with complex processes, teams distributed across locations, and evidence scattered across systems.

Fragmented Audits and Actions

Limited Visibility Into ISO Progress

Slow and Inconsistent RCA

CAPA Closure Delays and Gaps

Change Requests Without Traceability

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The only EHSQ solution built for the frontline with diret impact on management

One platform to manage Quality end-to-end

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Interface titled Create observation with options to report unsafe acts, unsafe conditions, or positive observations.
Dashboard showing 6 of 9 inspections completed with a circular progress icon and a total of 82 audits.

Audit readiness at any time

Centralize findings, evidence, and action plans

Faster investigations and resolution

Link observations, RCA and CAPA so nothing is lost between teams

Stronger compliance and continuous improvement

Standardize processes and prove effectiveness with traceable records

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Exploring all our solutions

Covering all your needs with a single solution

Glartek EHSQ Solutions
Audits Management
Plan audits, track objectives, capture evidence, and monitor closure to support ISO 45001 alignment.
Inspections Management
Run structured inspections with consistent checklists and clear follow-ups.
Observations
Capture shopfloor observations instantly and route them to the right owner.
Root Cause Analysis
Use standardized investigation workflows to identify real causes, not symptoms.
Corrective & Preventive Actions
Assign, track, verify, and close CAPAs with proof of effectiveness.
Management of Change
Control operational changes with approvals, risk evaluation, and audit trails.

Upholding quality on the day-today

Improving key metrics in quality

45%

Faster CAPA closure

50%

Less time preparing for audits

30%

Fewer repeat non-conformities

30%

Reduction in recordable incidents

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Testimonials

Hear it from our customers

"Glartek’s solution allows us to make an easier and faster diagnosis of the issues we have in our operations. The solution was very effective and met our expectations, so in the future our objective is to expand it to our different activities.”

Diana Tomázio
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Operational Quality

Make “zero deviations” a measurable reality

When quality workflows are standardized, improvement becomes measurable. Organizations that digitize audits, inspections, RCA, and CAPA reduce delays, improve traceability, and eliminate repeat findings by connecting every step, from the first observation to verified closure.

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