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LuminLogic is a 21 CFR Part 11 compliant SaaS solution that supports document, regulatory, quality, and risk management systems for medical device, pharmaceutical and biotech companies during the commercialization process.

LuminLogic Smart Enterprise Suite (SES) is designed specifically for regulated businesses. We built it to make FDA compliance, business process management and business communication easy and efficient for life science companies. Our trusted platform addresses compliance, quality management and regulatory concerns, and, thanks to the cloud, it comes with low risk and fast results.

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iec 606011 3rd edition a1, fda compliance strategies, 21 cfr part 11, cmm expertise, gxp, fda 21 cfr part 820, compliance audits, quality system development, risk remediation, iso, fda 21 cfr part 11 annex 11, hipaa, process validation strategies, iec 62304, software design control evaluations

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50
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