Skill Packages
Browse ready-made AI workflow skills for document elaboration, review, and structuring.
Change Order Impact Analyzer
Trace the technical impact of a proposed specification change across all related sections, disciplines, and procurement items to prevent cascading contradictions.
Learn MoreCharities Governance Code Compliance
Prepare the Charities Governance Code Compliance Record Form for the annual report to the Charities Regulator (Ireland). Aligns board minutes and policies with the six core principles and validates trustee term limits and rotation in the constitution.
Learn MoreChemical Safety (SDS Author)
Author and validate Safety Data Sheets (SDS / FISPQ) compliant with REACH Annex II, GHS, CLP Regulation, and ABNT NBR 14725-4 for EU and Brazilian markets. Validates the 16 mandatory sections and cross-checks chemical concentrations against CLP thresholds to auto-suggest H and P phrases.
Learn MoreCI Relationship Mapper (COBIT BAI10)
Draft the CMDB data model: how Hardware links to Software and Business Process. Ensures impact analysis is accurate. Includes orphan CI detector.
Learn MoreCIS Benchmark Mapper
Draft Secure Configuration Baselines (hardening guides) from CIS Benchmarks or STIGs into formal policy. Validates recurring Drift Analysis schedule (NIST CSF 2.0 PR.PS).
Learn MoreCIS Controls Implementation Author
Guided elaboration of CIS Controls v8 implementation plan — safeguard selection, IG1/IG2/IG3 alignment, and mapping to existing policies or controls.
Learn MoreCISA Circular Formatter (CPG 7.1)
Format incident data for CISA and SRMA reporting under CPG 7.1 and CIRCIA. Enforces 72-hour (covered incident) and 24-hour (ransomware) notification windows and validates Information Requirements so the first report is complete.
Learn MoreCitation Source Fidelity — Verificação Semântica de Citações
Validador de fidelidade semântica de citações. Dado um documento (TCC, dissertação, artigo, parecer jurídico, matéria jornalística) e as fontes originais em uploads/sources/, verifica se cada citação direta e cada paráfrase reflete fielmente o que a fonte realmente diz. Detecta distorção, paráfrase superficial, atribuição cruzada e citações cuja passagem-fonte não existe. Produz relatório com veredito por citação e explicação textual da divergência. Idiomas: pt-BR e en.
Learn MoreClinical claim evidence mapper
Persist a citation from every clinical claim (diagnosis, prior therapy, contraindication, lab value, score, outcome, coverage criterion, guideline) asserted in a drafted appeal or letter of medical necessity back to a chart excerpt. Blocks export of any drafting skill's output when claims are unmapped — the trust gate for all pilot-ready healthcare packets.
Learn MoreClinical Report Writing
Write comprehensive clinical reports including case reports (CARE guidelines), diagnostic reports (radiology, pathology, lab), clinical trial reports (ICH-E3, SAE, CSR), and patient documentation (SOAP notes, H&P, discharge summaries). Includes regulatory compliance and validation tools.
Learn MoreClinical Trial Protocol (ICH E6 R3)
Draft clinical trial protocols compliant with ICH E6(R3) and ICH E8(R1). Covers study design, objectives, endpoints, eligibility criteria, estimand framework (ICH E9(R1)), statistical analysis plan, safety monitoring, IDMC, RBQMS, and regulatory submission requirements (FDA IND / EU CTR 536/2014 via CTIS) for all study phases and therapeutic areas.
Learn MoreClinical Trial Protocol (ICH E6(R3) GCP)
Draft and validate clinical trial protocols per ICH E6(R3) Good Clinical Practice and ICH E8(R1) General Considerations for Clinical Studies. Ensures the protocol contains all required elements for ethics committee / IRB submission and regulatory filing (EMA, FDA IND, ANVISA).
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