Out With Paper Travelers, In With eDHR
Audit-Ready Execution Evidence
Medical Devices
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ISO 17025 – Laboratory Accreditation
Accurate. Accredited. Assured.
21 CFR Part 820 – Medical Devices
Verified. Validated. Vigilant.
Electronic Device History Record (eDHR)
Digitized Batch Control
Certified. Controlled. ISO 13485.
Regulated. Recorded. Ready.
LIMS Integration for V5 MES & QMS
Automated lab-to-batch control