Pharmaceutical Quality & Training Software
Choose individual GMP quality modules, a complete electronic Quality Management System, or standalone Training Management Software.
Electronic Document Management
Controlled documents, revisions, approvals and document lifecycle management.
Deviations & Investigations
Deviation investigations, root cause analysis and QA review.
CAPA Management
Corrective and preventive actions with effectiveness verification.
Change Control
Controlled changes, impact assessments and approval workflows.
Supplier Qualification
Supplier registration, risk assessments and qualification workflows.
Process Compliance
Process compliance records, monitoring and quality oversight.
Complete QMS Suite
Integrated access to all available QMS modules under one license.
Standalone Training Management
SOP training, employee assignments, retraining and compliance dashboards.
Flexible GMP Software Licensing
Start with individual modules or select the complete QMS suite. Customer-specific trial environments and module-level audit controls are being prepared.
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