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compliance-briefing-kit

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🇺🇸

Original

English

🇨🇳

Translation

Chinese

Compliance Briefing Kit Skill

合规简报工具Skill

When to Use

使用场景

Kicking off HIPAA/FDA-compliant campaign reviews.
Preparing legal/medical reviewers with complete context.
Auditing historical campaigns for documentation completeness.

启动符合HIPAA/FDA标准的营销活动审核。
为法务/医疗审核人员提供完整的背景信息。
审核历史营销活动的文档完整性。

Framework

框架

Campaign Snapshot – objectives, audiences, channels, timelines, owners.
Data & Consent Map – data sources, identifiers, consent method, retention policy.
Claims & Evidence – value propositions, clinical proof, disclaimers, risk statements.
Regulatory Checklist – HIPAA, FDA (DTC/HCP), FTC, regional privacy, accessibility steps.
Approval Workflow – reviewers, SLAs, escalation path, expiration date.

营销活动概览 – 目标、受众、渠道、时间线、负责人。
数据与同意记录 – 数据来源、标识符、同意方式、留存政策。
声明与证据 – 价值主张、临床证据、免责声明、风险说明。
合规检查清单 – HIPAA、FDA（直接面向消费者/医疗保健专业人员）、FTC、区域隐私、无障碍措施。
审批工作流 – 审核人员、服务水平协议（SLA）、升级路径、到期日期。

Templates

模板

Compliance intake form (fillable PDF/Notion) with required fields.
Reviewer packet structure (assets, claims, data flows, prior approvals).
Decision log sheet with timestamps and attachments.

包含必填字段的合规收集表单（可填写PDF/Notion格式）。
审核人员数据包结构（资产、声明、数据流、过往审批记录）。
带时间戳和附件的决策记录表。

Tips

提示

Require complete claims/evidence attachments before routing to legal.
Include version history to track copy or asset changes during review.
Pair with
```
run-compliance-review
```
for automated routing + documentation.

在提交给法务审核前，要求附上完整的声明/证据附件。
包含版本历史记录，以跟踪审核期间文案或资产的变更。
搭配
```
run-compliance-review
```
使用，实现自动流转 + 文档记录。