Operate your quality management system — controls, non-conformities, CAPA, supplier quality and audits — in line with ISO 9001, 13485 and 22000.
Everything a QMS needs — controls, non-conformities, CAPA and audits — all within the same platform as the rest of your governance.
Documented procedures relating to controls and records.
Record, categorise and resolve non-conformities.
Corrective and preventive actions, including those responsible and deadlines.
Supplier assessment, audits and quality scoring.
Plan and carry out internal quality audits, recording the findings.
Version-controlled documents and approvals.
Quality controls specific to medical devices.
HACCP and food safety controls.
Run a CAPA once and iComply highlights it in all the quality standards that refer to it — without any duplication of effort.
Scope & diagnosisDefine the scope and carry out a GAP analysis against the selected standards.
Map controlsSelect controls; iComply automatically maps them to each relevant framework.
Collect evidenceAssign tasks, upload evidence once and reuse it across all requirements.
Audit & monitorCarry out audits, track CAPA and monitor compliance on an ongoing basis.
Internal audit, findings and CAPA.
Supplier risk, due diligence and the Data Protection Act.
View all governance domains in a single platform.
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