UK/US consultancy for medical device software FDA submissions, documented from public research.
Visit qmlogic.comPublic-tier claims with issuer citations; registry verification pending.
Certifications are held by individuals, never organizations. Org-level status below is a DERIVED rollup of named holders, the org claims nothing its holders do not hold. Issuer directories (GIAC, (ISC)², ISACA) list individual certificate holders with expiration dates, registry lookups resolve at the named-holder level and require no carrier data.
No certifications documented for this firm.
None documented
Not documented
Documented from public research (firm website and cited public pages, read September 2026).
Publishes end-to-end FDA 510(k) consulting for medical device software including 21 CFR 820.30 and Part 11. (cited sources on file, September 2026).
Sourced from public research; the platform's full verification pass is pending.
No publicly documented case work was found on the firm's own site at the time of our research. Some firms publish engagement details under NDA restrictions; some simply do not publish. The absence of documented work is a fact, not a judgment.
