Loading...
Loading...
Found 4 Skills
Comprehensive toolkit for preparing ISO 13485 certification documentation for medical device Quality Management Systems. Use when users need help with ISO 13485 QMS documentation, including (1) conducting gap analysis of existing documentation, (2) creating Quality Manuals, (3) developing required procedures and work instructions, (4) preparing Medical Device Files, (5) understanding ISO 13485 requirements, or (6) identifying missing documentation for medical device certification. Also use when users mention medical device regulations, QMS certification, FDA QMSR, EU MDR, or need help with quality system documentation.
Эксперт по compliance отчётам. Используй для SOX, GDPR, HIPAA, SOC 2 аудитов и документации соответствия.
Standardized template for campaign compliance intake, reviews, and approvals.
Advertising compliance review skill, designed to check whether advertising materials comply with the Advertising Law of China and relevant regulations. Applicable scenarios: (1) When users submit advertising copy or materials for compliance review; (2) When users mention keywords such as "advertising review", "advertising compliance", "advertising law inspection"; (3) When users require to check if there are illegal or non-compliant risks in advertising content; (4) When users submit advertisements from industries including real estate, food, medical care, pharmaceuticals, internet etc. for special review. The review basis covers the Advertising Law, Anti-Unfair Competition Law and industry-specific regulations.