Skill Packages
Browse ready-made AI workflow skills for document elaboration, review, and structuring.
CSRD Double Materiality Assessment (ESRS 1 §3)
Run an ESRS 1 §3 Double Materiality Assessment end-to-end: scope and methodology memo, stakeholder engagement plan and log, IRO long-list, impact and financial scoring rubrics, value-chain coverage, ESRS topic and sub-topic disclosure scoping, ESRS Set 1 datapoint gap log, board approval pack, and an ISAE 3000 (Revised) assurance evidence file — aligned with EFRAG IG-1, IG-2, and IG-3.
Cyber Threat Information Sharing (DORA Art. 45)
Draft information sharing arrangements for exchanging cyber threat intelligence per DORA Art. 45, covering participation agreements, data protection safeguards, sharing protocols (TLP, STIX/TAXII), and governance.
Learn MoreCybersecurity Incident Response Plan (Sector & State-Specific)
Draft a cybersecurity Incident Response Plan aligned with NIST SP 800-61r3, tailored to industry sector (HIPAA, GLBA, PCI DSS, FERPA, NERC CIP) and state breach notification laws. Includes detection playbooks, escalation procedures, and state-by-state notification timeline matrix.
Data Privacy — AIPD (CNIL Standard)
Conduct a Privacy Impact Assessment (AIPD) under the CNIL standard for France (RGPD). Three-step methodology: Context, Principles, Risks. Validates retention periods against CNIL 'droit à l'oubli' (right to erasure).
Learn MoreData Processing Agreement (DPA) — SCC & sub-processor sync
Draft the legal annex for DPAs governing controller–processor data transfers under GDPR and CCPA. Inserts the correct Standard Contractual Clauses by data importer country and validates sub-processor list against the privacy portal.
Learn MoreDenial intake normalizer
Parse payer denial letters, EOBs, Medicare Advantage IDNs, NOMNC/DENC, and appeal forms into a structured case.json. Classifies the denial, routes the appeal type, and computes the appeal deadline — the intake step for every downstream denial-appeal and prior-auth skill.
Learn MoreDesign Dossier Elaborator
Guided elaboration of design dossier, technical file, or device master record sections for medical devices: device classification, risk summary (ISO 14971:2019), essential principles (GSPR), labelling/IFU, clinical evaluation, post-market surveillance, and traceability per EU MDR 2017/745 Annex II and FDA QMSR (21 CFR Part 4).
DiGA Fast-Track
Prepare and validate Fast-Track applications for listing Digital Health Applications (DiGA) in the BfArM directory per DiGAV. Cross-checks clinical study protocols against claimed Positive Versorgungseffekte and audits technical documentation for ISiK interoperability standards compliance.
Learn MoreDigital Operational Resilience Testing Program (DORA)
Design the resilience testing program required by DORA Arts. 24-27, covering basic testing (vulnerability assessments, penetration testing, scenario-based tests) and advanced TLPT for significant entities per RTS 2025/1190.
Learn MoreDoc Co-Authoring
Guide users through a structured workflow for collaboratively writing documents, proposals, specs, and decision docs. Uses a three-stage process: context gathering, iterative refinement, and reader testing.
Learn MoreDoc Oferta FIDC - Documentos da Oferta
Elaboração dos documentos de oferta pública de cotas de FIDC: prospecto, regulamento, lâmina, aviso ao mercado, anúncios de início e encerramento, e resumo mensal, conforme Resolução CVM 160/2022
DOCX Tools
Professional DOCX tools for creating, editing, and manipulating Word documents. Create new .docx with full style control, edit existing files at the XML level, handle tracked changes and comments, convert between formats, and validate OOXML structure.
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