Create a compliant Appendix A slide package offering IP landscapes, freedom-to-operate memos and regulatory readiness roadmaps to satisfy diligence requests from biotech-focused VCs

Generate create a compliant appendix a slide package offering ip landscapes, freedom-to-operate memos and regulatory readiness roadmaps to satisfy diligence requests from biotech-focused vcs for Scientific Research and Development Services industry

Scientific Research and Development Services

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Upload patent applications, office action responses, prior-art search results, or invention disclosures as the foundation for Appendix A. Supports full IP portfolio analysis.
Choose the major life-science category to guide claim construction, regulatory pathway, and competitive landscape analysis—directly informs FTO memo organization.
Specify the major US FDA divisions or ex-US pathways relevant to this asset; drives regulatory readiness section and milestone timelines.
Align diligence depth to current fundraise: Seed/Series A focuses on IP novelty; Series B/C adds regulatory threshold data; IPO stage requires full manufacturing control narratives.
List patent families, branded product names, and assignee companies whose patents must be mapped; critical for FTO opinion and white-space charts.
Define risk tolerance to tailor claim-depth and mitigation notes in Appendix A; closely tied to term-sheet terms requested by VCs.
Anticipated dates or quarters for pre-IND/IND, end-of-Phase 2, Type C meetings; anchors Gantt charts for VC diligence timeline.
Choose final deliverable style to match VC data-room standards; dictates slide count, executive-summary orientation, and red-flag callouts.
Insert law-firm docket number or prior FTO memo reference for consistency; ensures alignment with already-run searches.