ClawStack

Fda Consultant Specialist

BFair

🛠️ Dev Tools · by alirezarezvani

205
upvotes

FDA regulatory consultant for medical device companies. Provides 510(k)/PMA/De Novo pathway guidance, QSR (21 CFR 820) compliance, HIPAA assessments, and device cybersecurity. Use when user mentions FDA submission, 510(k), PMA, De Novo, QSR, premarket, predicate device, substantial equivalence, HIPAA medical device, or FDA cybersecurity.

dev-tools

Install

$openclaw plugins install alirezarezvani/fda-consultant-specialist

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Security Analysis

Score: 69/100
BFair
Security Scan10/30
Network Safety15/15
Community Trust5/10
Permissions14/20
Author Reputation15/15
Auditability10/10

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