What problem does it solve? Creating a consulting-grade regulatory training PPT for medical device topics (FDA 510(k), CE MDR, NMPA registration) requires coordinating content structure, visual design, and PPTX assembly across multiple AI tools. This Skill produces three reusable, topic-adapted instruction documents so users can generate a consistent, professional deck without writing prompts from scratch. ## Core Features & Use Cases - Instruction 1 (Content Structure): Adapts a canonical 15-page consulting-style outline (background, criteria, application path, evidence strategy, action plan) to any regulatory topic. - Instruction 2 (Visual Style): Produces 3-4 visual style concepts (Professional, Modern, Technical, Premium) across 6 page types via ImageGen, using company brand colors. - Instruction 3 (Editable PPTX Assembly): Directs python-pptx generation of fully editable slides (text boxes, tables, shapes, speaker notes) rather than image-embedded slides. - Use Case: Ask for PPT instructions on "EU Breakthrough Device Designation" and receive a single Markdown file with all three adapted instruction sets ready to paste into any AI tool. ## Quick Start Generate a complete set of PPT instructions for the topic "FDA 510(k) Submission Strategy".
