Legal-AI skills in 🇺🇸 United States

984 skills, across 45 practice areas.

Expert Witness Impeachment

Apache-2.0United StatesLitigation

Surfaces inconsistencies, opinion shifts, methodological flaws, and credential discrepancies across expert reports, transcripts, CVs, and publications for impeachment, cross-examination, and exclusion motions. Trigger when the user references expert impeachment, expert report analysis, Daubert or Frye challenges, deposition prep against an expert, or credibility attacks on opposing expert witnesses.

Expert Witness Impeachment Analysis

Apache-2.0United StatesLitigation

Analyzes expert witness materials (reports, depositions, CVs, publications) to identify inconsistencies, opinion drift, and methodological failures for impeachment. Produces a prioritized inconsistency register, cross-examination questions, and Daubert/Frye challenge assessment. Use when challenging expert reliability or credibility during discovery, pre-trial, or trial in commercial litigation.

Expert Witness Medical Records Omissions Analysis

Apache-2.0United StatesPersonal injury

Identifies medical records an expert witness failed to review, cite, or address by cross-referencing the expert's materials-reviewed list against the full case record set. Produces a tiered omissions register, methodology critique, bias analysis, and strategic recommendations for cross-examination and exclusion motions. Use in personal injury or medical malpractice litigation when challenging or defending expert credibility during discovery, pre-trial, or trial preparation.

Expert Witness Report Analysis

Apache-2.0United StatesLitigation

Critiques opposing expert witness reports for admissibility challenges, disclosure deficiencies, and cross-examination vulnerabilities. Triggers when the user provides an expert report for analysis, needs Daubert/Frye assessment, requests a motion to exclude or limit expert testimony, or prepares deposition or trial cross-examination of an opposing expert.

Expert Witness Report Summary

Apache-2.0United StatesLitigation

Produces structured, citation-ready summaries of U.S. expert witness reports for litigation. Captures qualifications, assignment, methodology, materials, findings, opinions, assumptions, limitations, and quantitative results with pinpoint citations. Use when summarizing expert reports, preparing for depositions or trial, reviewing expert disclosures, or planning cross-examination.

Expert Witness Report Summary

Apache-2.0United StatesLitigation

Generates structured, citation-anchored summaries of expert witness reports for depositions, hearings, and trial preparation. Distills qualifications, methodology, opinions, assumptions, and quantitative findings into a navigable reference. Use when summarizing expert witness reports, retained expert disclosures, or rebuttal expert reports in US litigation.

Export Administration Regulations (EAR) Compliance Skill

MITUnited StatesSanctions

Export Administration Regulations (EAR, 15 CFR Parts 730-774) compliance advisor — ECCN classification across all 10 CCL categories and 5 product groups (A-E), EAR99 determination, jurisdiction analysis (EAR vs ITAR order of review), license requirement analysis via Country Chart, all license exceptions (LVS, GBS, CIV, TMP, RPL, GOV, TSU, ENC, TSR, APP, BAG, AVS, ACE), end-user/end-use controls (Entity List, Denied Persons List, Unverified List, MEU List), deemed export rules, Foreign Direct Product Rule (FDPR), de minimis thresholds, 10 General Prohibitions, SNAP-R license applications, voluntary self-disclosure, civil/criminal penalties, Export Compliance Program (ECP) design, and EAR vs ITAR jurisdiction determination. Use for any dual-use export control, CCL classification, or BIS compliance question.

Export Compliance Program (ECP) Manual

Apache-2.0United StatesSanctions

Drafts an audit-ready Export Compliance Program manual covering EAR, ITAR, and OFAC requirements. Use when creating or updating an export compliance policy, international trade compliance program, or preparing enforcement defense documentation for regulatory review.

Exporter of Record (EOR) Agreement

Apache-2.0United StatesSanctions

Drafts a U.S.-compliant Exporter of Record (EOR) Agreement appointing a third party as USPPI for international export transactions. Allocates compliance obligations under EAR, ITAR, OFAC, and CBP with denied-party screening, AES/EEI filing, indemnification, and record retention. Use when drafting EOR appointments, export compliance service agreements, or logistics outsourcing for cross-border shipments.

Expungement Petition

Apache-2.0United StatesCriminal

Drafts jurisdiction-specific petitions for expungement or sealing of criminal records. Covers caption construction, statutory eligibility analysis, rehabilitation narratives, and prayer for relief. Use when drafting expungement petitions, record-sealing motions, set-aside petitions, or certificates of rehabilitation in post-conviction proceedings.

Extracting Case Data for SC-100 Form

MITUnited StatesLitigation

Use this skill to extract and organize case data from a natural language case description for filling the SC-100 form. Maps case facts to form fields.

Fairness Hearing Notice

Apache-2.0United StatesLitigation

Drafts FRCP 23(e)-compliant fairness hearing notices for class action settlements. Covers settlement terms, opt-out rights, objection procedures, and hearing logistics. Use when notifying class members of a proposed settlement pending court approval.

Family Law Summons

Apache-2.0United StatesFamily

Drafts procedurally compliant family law summons for dissolution, custody modification, support enforcement, and other domestic proceedings. Covers jurisdiction-specific formatting, mandatory statutory warnings (ATROs), response deadlines adjusted by service method, service of process instructions, and proof of service sections. Use when initiating family law litigation, preparing summons for service, or drafting notice documents for domestic relations cases.

Family Limited Partnership (FLP) Agreement

Apache-2.0United StatesTrusts and estates

Drafts Family Limited Partnership agreements for estate planning and intergenerational wealth transfer. Ensures IRS enforceability under IRC §2036 with legitimate business purpose, valuation discounts, and senior-generation control. Use when drafting FLP agreements, family partnership documents, or estate planning partnership structures.

FAR-Compliant Subcontract Agreement

Apache-2.0United StatesGovernment contracts

Drafts FAR-compliant subcontract agreements between prime contractors and subcontractors under U.S. federal government prime contracts. Handles mandatory flow-down of FAR/DFARS/agency clauses, contract-type pricing, security/clearance, IP/data rights, and termination. Use when drafting government subcontracts, FAR flow-down clauses, or prime-sub agreements.

Farmout Agreement

Apache-2.0United StatesEnergy

Drafts U.S. upstream oil and gas farmout agreements transferring working interests through earn-in obligations. Use when drafting farmout/farm-in agreements, defining earning well requirements, negotiating farmee/farmor terms, integrating JOA/AMI provisions, or handling reassignment and reversion mechanics.

FCPA Compliance Policy

Apache-2.0United StatesWhite collar

Drafts an implementable Foreign Corrupt Practices Act (FCPA) Compliance Policy for U.S.-jurisdictional corporations with international operations. Covers anti-bribery provisions (15 U.S.C. §§ 78dd-1 through -3), accounting provisions (15 U.S.C. §§ 78m(b)(2)(A)-(B)), gift thresholds, tiered third-party due diligence, internal controls, training, and whistleblower protections. Incorporates DOJ/SEC Resource Guide guidance. Use when drafting or updating an FCPA policy, anti-bribery compliance program, corporate ethics policy, or international corruption risk framework.

FDA 510(k) Premarket Notification

Apache-2.0United StatesLife sciences

Drafts FDA 510(k) Premarket Notification submissions demonstrating substantial equivalence under 21 CFR Part 807. Supports Traditional, Special, and Abbreviated pathways. Use when preparing Class II medical device regulatory filings, substantial equivalence analyses, or FDA premarket submissions.

FDA Establishment Registration & Device Listing

Apache-2.0United StatesLife sciences

Drafts FDA Establishment Registration and Device Listing documents compliant with 21 CFR Part 807. Structures filings with establishment details, owner/operator information, device inventories, compliance certifications, and signature blocks mirroring FDA Form 2830. Triggers on initial registrations, annual renewals, listing updates, or foreign establishment filings requiring US agent designations.

FDA Food Facility Registration

Apache-2.0United StatesRegulatory

Drafts an FDA Food Facility Registration under FSMA and 21 CFR Part 1, Subpart H (21 U.S.C. 350d). Covers facility identity, food product categories, U.S. agent designation for foreign facilities, and certification language. Use when preparing new FDA facility registrations, biennial renewals, or registration updates for domestic or foreign food facilities.

FDA Labeling Compliance Review

Apache-2.0United StatesRegulatory

Conducts FDA labeling compliance reviews for drugs, foods, dietary supplements, and medical devices. Analyzes principal display panels and information panels against FDCA, 21 CFR, and FDA guidance to identify misbranding risks, claims violations, and mandatory disclosure gaps. Use when reviewing product labels, auditing FDA compliance, assessing labeling risk, or preparing for FDA submission.

FDA MedTech Compliance Auditor

MITUnited StatesLife sciences

FDA MedTech Compliance Auditor workflow skill. Use this skill when the user needs Expert AI auditor for Medical Device (SaMD) compliance, IEC 62304, and 21 CFR Part 820. Reviews DHFs, technical files, and software validation and the operator should preserve the upstream workflow, copied support files, and provenance before merging or handing off.

FDA MedTech Compliance Auditor

MITUnited StatesLife sciences

Expert AI auditor for Medical Device (SaMD) compliance, IEC 62304, and 21 CFR Part 820. Reviews DHFs, technical files, and software validation.

FDA MedTech Compliance Auditor

MITUnited StatesLife sciences

FDA MedTech Compliance Auditor workflow skill. Use this skill when the user needs Expert AI auditor for Medical Device (SaMD) compliance, IEC 62304, and 21 CFR Part 820. Reviews DHFs, technical files, and software validation and the operator should preserve the upstream workflow, copied support files, and provenance before merging or handing off.