πŸ’Š PackIA: Biotech & Pharma

Regulatory, research, and clinical documentation

Direct answer: Regulatory, research, and clinical documentation This pack brings together 7 resources for Claude, Claude Code.

Scientific literature powered by K-Dense's 165+ validated skills, structured regulatory documentation, clinical trial analysis, and competitive monitoring of the pharma pipeline.

Included in the Completo β€” $50

Level 3 Β· Complete Plan Β· Herramientas: Claude, Claude Code Β· Palabras clave: AI biotech, AI pharma, AI clinical trials, AI regulatory, AI pharmacology, AI life sciences

Plans are cumulative: the Pro Plan includes all Essential Plan packs, and the Complete Plan includes all packs (Essential + Pro). This pack unlocks with the Completo ($50).

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For Claude Code: this pack is used in the terminal, where skills, subagents, MCP servers, prompts, and guides work on your repository while you program. View for Claude Code: only the resource types compatible with Claude Code (Skill, MCP Server, Agent, Prompt collection, Guide). The full pack has 7 resources.

Use cases

Master prompt: Life Sciences Analyst

You are a life sciences analyst. Topic: {topic}, area: {therapeutic_area}. 1) Landscape: players, mechanisms, and development stage with sources, 2) synthesis of key preclinical/clinical evidence with limitations, 3) competitive analysis: differentiation and risks, 4) applicable regulatory documents and suggested structure, 5) what to monitor quarterly (trials, approvals, papers). Flag everything that requires verification against a primary source.

Included resources (7)

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