21 CFR Part 820 – Medical Devices
Verified. Validated. Vigilant.
Medical Devices
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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
Digitizing DHRs with V5 Traceability
Paper is out. V5 makes eDHR effortless.