「iso-27001」の検索結果

Router/index for the 15 regulatory & quality-management skills bundled in this plugin (ISO 13485 QMS, EU MDR 2017/745, FDA submissions under QMSR, ISO 14971 risk, CAPA, document control, ISO 27001/ISMS, ISO 42001 AIMS, EU AI Act, GDPR/DSGVO, SOC 2, auditing). Use when a compliance request doesn't obviously match one skill and you need to pick the right one (e.g., 'prepare us for an ISO 13485 audit', 'is my AI system high-risk under the AI Act').

日本語の概要は準備中です。原文の説明を表示しています。

ISMS auditing for ISO 27001 compliance, control assessment, and certification support. Use for ISMS audit programs, internal/external ISO 27001 audits, ISO 27002 Annex A control testing, and Stage 1/Stage 2 certification audits.

日本語の概要は準備中です。原文の説明を表示しています。

ISO 27001:2022 ISMS implementation and cybersecurity governance for HealthTech and MedTech. Use for ISMS design, risk assessment per Clause 6.1.2, Annex A controls, ISO 27001 certification, security audits, and incident response.

日本語の概要は準備中です。原文の説明を表示しています。

Guides ISO 27701 Privacy Information Management System implementation extending ISO 27001/27002. Covers Clause 5 PIMS-specific requirements, Clause 6 PIMS guidance for ISO 27002, Clause 7 PII controller guidance (Annex A), Clause 8 PII processor guidance (Annex B), gap assessment, and certification path. Keywords: ISO 27701, PIMS, privacy management system, ISO 27001 extension, certification, Annex A, Annex B.

日本語の概要は準備中です。原文の説明を表示しています。

ISO/IEC 27001:2022 is the international standard for establishing, implementing, maintaining, and continually improving an Information Security Management System (ISMS). bu skill covers the complete

日本語の概要は準備中です。原文の説明を表示しています。

12 regulatory & QM agent skills and plugins for Claude Code, Codex, Gemini CLI, Cursor, OpenClaw. ISO 13485 QMS, MDR 2017/745, FDA 510(k)/PMA, ISO 27001 ISMS, GDPR/DSGVO, risk management (ISO 14971), CAPA, document control, auditing. Python tools (stdlib-only).

日本語の概要は準備中です。原文の説明を表示しています。