Bukalemun Health
Manage laboratory, quality and pharma workflows through auditable, controlled and integrated processes.

A shared digital foundation for regulated processes
Bukalemun Health manages laboratory and quality records with controlled access, approvals, revisions and audit trails on one platform.
Modular capabilities
Deploy together or progressively based on your scope.
QMS, deviation, CAPA and change control
Stability and method validation
Training, maintenance and calibration
Electronic approval and audit trail
Instrument, ERP and document integrations
Health process backbone
Laboratory and quality records use the same access, approval and audit principles.
Record
A sample, quality event or related operational record is opened in a controlled way.
Workflow
Tasks, tests, reviews and approvals are routed to responsible roles.
Control
Access, revision, evidence and state rules are applied.
Reporting
Approved records become available for reporting and enterprise integration.
Frequently asked questions
Can LIMS and QMS be used together?
Yes. A shared core lets laboratory and quality workflows use common identity, workflow and integration principles.
How are regulatory requirements handled?
Platform capability is separated from organisational validation and regulatory responsibility; project requirements are confirmed explicitly.
Define your Health scope
Model your laboratory and quality workflows using the right modules for your requirements.