Regulatory & privacy compliance agent skills
297 skills in Regulatory & privacy compliance.
Top skills
- Customs Trade Compliance 通関書類、関税分類、関税最適化、制限当事者スクリーニング、複数の法域にわたる規制コンプライアンスのための成文化された専門知識。15年以上の経験を持つ貿易コンプライアンス専門家に情報。HS分類ロジ…
- Hipaa Compliance HIPAA準拠実装、セキュリティ対策、監査ログ、およびデータ保護戦略。
- Customs Trade Compliance 海关文件、关税分类、关税优化、受限方筛查以及多司法管辖区法规合规的编码化专业知识。由拥有15年以上经验的贸易合规专家提供。包括HS分类逻辑、Incoterms应用、自贸协定利用以及罚款减免。适用…
- Hipaa Compliance 针对医疗隐私和安全工作的HIPAA特定入口点。当任务明确围绕HIPAA、PHI处理、受保实体、BAA、违规态势或美国医疗合规要求时使用。
- Customs Trade Compliance Codified customs and trade compliance expertise — HS/HTS tariff classification with GRI rules, co…
- Gdpr Compliant Apply GDPR-compliant engineering practices across your codebase.
- Skill Card Generator Use only to generate or update a governance skill card for a specified existing agent skill direc…
- Ai Act Readiness /cs:ai-act-readiness <system> — EU AI Act 6-question forcing interrogation.
- Aims Audit /cs:aims-audit <scope> — ISO/IEC 42001 AIMS internal-audit 6-question forcing interrogation.
- Compliance Os Compliance OS — meta-orchestrator that lets compliance teams CONFIGURE which frameworks apply, CO…
- Compliance Readiness /cs:compliance-readiness <program> — Multi-framework compliance officer 6-question forcing interr…
- Fda Qsr Audit Prep /cs:fda-qsr-audit-prep <scope> — FDA 21 CFR 820 (QSR / QMSR) audit 6-question forcing interrogation.
- Gdpr Audit Prep /cs:gdpr-audit-prep <scope> — GDPR audit 6-question Article-cited forcing interrogation.
- Iso13485 Audit Prep /cs:iso13485-audit-prep <scope> — ISO 13485 QMS audit 6-question forcing interrogation.
- Iso27001 Audit Prep /cs:iso27001-audit-prep <scope> — ISO 27001 ISMS audit readiness 6-question forcing interrogation.
- Soc2 Audit Prep /cs:soc2-audit-prep <scope> — SOC 2 Type II readiness 6-question forcing interrogation.
- Eu Ai Act Specialist EU AI Act (Regulation (EU) 2024/1689) operational compliance for compliance teams.
- Iso42001 Specialist ISO/IEC 42001:2023 AI Management System (AIMS) specialist for compliance teams running internal a…
- Capa Officer CAPA system management for medical device QMS.
- Fda Consultant Specialist FDA regulatory consultant for medical device companies.
- Gdpr Dsgvo Expert GDPR and German DSGVO compliance automation.
- Mdr 745 Specialist EU MDR 2017/745 compliance specialist for medical device classification, technical documentation,…
- Qms Audit Expert ISO 13485 internal audit expertise for medical device QMS.
- Quality Documentation Manager Document control system management for medical device QMS.