From 5f63dbf10ba6539c2ca830300a52b25a0b500709 Mon Sep 17 00:00:00 2001 From: alirezarezvani <5697919+alirezarezvani@users.noreply.github.com> Date: Fri, 30 Jan 2026 03:13:41 +0000 Subject: [PATCH] chore: sync codex skills symlinks [automated] --- .codex/skills-index.json | 4 ++-- 1 file changed, 2 insertions(+), 2 deletions(-) diff --git a/.codex/skills-index.json b/.codex/skills-index.json index 009e375..e6f3ce6 100644 --- a/.codex/skills-index.json +++ b/.codex/skills-index.json @@ -75,7 +75,7 @@ "name": "senior-frontend", "source": "../../engineering-team/senior-frontend", "category": "engineering", - "description": "Comprehensive frontend development skill for building modern, performant web applications using ReactJS, NextJS, TypeScript, Tailwind CSS. Includes component scaffolding, performance optimization, bundle analysis, and UI best practices. Use when developing frontend features, optimizing performance, implementing UI/UX designs, managing state, or reviewing frontend code." + "description": "Frontend development skill for React, Next.js, TypeScript, and Tailwind CSS applications. Use when building React components, optimizing Next.js performance, analyzing bundle sizes, scaffolding frontend projects, implementing accessibility, or reviewing frontend code quality." }, { "name": "senior-fullstack", @@ -195,7 +195,7 @@ "name": "fda-consultant-specialist", "source": "../../ra-qm-team/fda-consultant-specialist", "category": "ra-qm", - "description": "Senior FDA consultant and specialist for medical device companies including HIPAA compliance and requirement management. Provides FDA pathway expertise, QSR compliance, cybersecurity guidance, and regulatory submission support. Use for FDA submission planning, QSR compliance assessments, HIPAA evaluations, and FDA regulatory strategy development." + "description": "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." }, { "name": "gdpr-dsgvo-expert",