EU AI Act Pharmacovigilance Implications: Mastery of EU AI Act requirements applicable to pharmacovigilance including risk classification cate...
Domain: D12 - Industry & Regulatory Type: Knowledge Proficiency Level: L4 (Proficient - Independent practice) Bloom Level: Analyze
Mastery of EU AI Act requirements applicable to pharmacovigilance including risk classification categories for AI systems, conformity assessment obligations, transparency requirements for automated decision-making, and post-market monitoring expectations. Understanding of high-risk AI system designation criteria relevant to drug safety, documentation requirements under Annex IV, and EMA preparations for AI Act implementation in medicines regulation.
When this skill is activated, Claude should:
Generated from PV KSB Framework v1.0 | 2025-12-31