Claude Skills by sunyifeisb-art

Redline a proposed side letter on behalf of an LP client by reference to the LP's investment policy, the governing fund documents, and prior fund precedent, producing a marked-up draft with a cover memo that prioritizes changes and identifies the LP's policy basis for each position.

Draft a private placement memorandum for a fund offering using a prior fund's PPM as a structural template, reconciling all source documents into a single consistent offering document with the required disclosure sections for a private fund offering.

Draft a complete set of side letters for multiple investors at a fund closing, along with a campaign summary memo and an MFN disclosure schedule, where investors have potentially conflicting requests, some provisions may exceed the side-letter policy, and the MFN cascade must be analyzed across the full investor group.

Draft side letters for multiple investors at a fund closing, produce a campaign summary memo with MFN cascade analysis, and prepare an MFN disclosure schedule. The task requires distinguishing MFN-eligible provisions from carved-out provisions and resolving investor-specific issues using the governing side-letter policy and the fund’s operating documents.

Draft a subscription agreement for a governmental plan investor's commitment to a fund and prepare an issues memo identifying cross-document inconsistencies, where the investor's regulatory status, tax treatment, and investment authorization present distinct issues that must each be accurately addressed.

Mark up a prior fund LPA precedent in tracked changes to conform to a new fund's term sheet, adding required new sections, and flagging open questions and valuation methodology concerns with partner notes.

Draft a seller-protective transfer agreement for a secondary market sale of a fund interest, incorporating protections and closing mechanics drawn from the governing fund documents, related side letters, consent materials, and capital account records.

Extract and cross-reference key terms from subscription documents and a related summary into a standardized term extraction report, flagging inconsistencies across documents and capturing the operative language and regulatory characterization required for each investor representation.

Extract all pricing-relevant terms from a secondary LP interest transfer document set into a structured pricing term sheet, with an appended issues log identifying discrepancies, ambiguities, and gaps across the documents.

Extract all reporting obligations from an investment advisory agreement and companion documents into a consolidated reporting obligation matrix, and identify structural and compliance issues including sequencing dependencies, deadline ambiguities, and gaps between the adviser's ongoing obligations and the agreement's periodic reporting cadence.

Review a Form ADV Part 2A brochure against supporting compliance and fund documents and produce a findings memo organized by item number with severity ratings and remediation recommendations for each identified deficiency.

Review a draft investment advisory agreement on behalf of an investor client and produce an issues memo identifying material deficiencies, with severity ratings, legal authority citations, and recommended resolutions for each issue.

Review a limited partnership interest transfer agreement as counsel to the fund or general partner and produce an issues memo identifying material concerns and consent conditions by comparing the transfer documents against the governing partnership agreement, related side arrangements, portfolio-company information, and capital account or comparable transfer-supporting records.

Review subscription documents for a large institutional investor and produce a comprehensive issues memo for the fund sponsor identifying material legal, regulatory, and commercial concerns before the investor is admitted as a limited partner.

Review a private equity fund LPA from an LP investor's perspective and produce an issues memo with severity ratings and negotiation recommendations for provisions that deviate from market standard or the LP's investment guidelines.

Review a registered investment adviser's compliance manual against applicable regulatory requirements and supporting materials, then produce an issues memo identifying regulatory and operational deficiencies, with severity ratings and remediation recommendations for each issue identified.

Draft counsel responses to an LP comment memo on a fund agreement, completing the response column with a clear accept/partial-accept/reject decision, a concise rationale, and proposed revised language for each accepted or partially accepted comment.

Review an LP comment package and accompanying LPA markup, then produce a GP counsel response memo that includes a summary matrix, comment-by-comment responses with accept/modify/reject decisions, precedent-based analysis where relevant, and an appendix cross-referencing comments to the applicable LPA sections.

Review a Form ADV Part 2A brochure against supporting records and produce an issues memo organized by Item number with severity ratings, regulatory basis citations, and remediation recommendations with timelines for each deficiency.

Identifies structural and documentary gaps in a healthcare data privacy compliance program using incident records, vendor tracking, audit findings, and governance minutes to produce a remediation-focused memorandum.

Reviews a site’s redline of a sponsor clinical trial agreement against a negotiation playbook to classify changes by risk level and recommend negotiating positions, with attention to intellectual property, indemnification, insurance, audit rights, publication, assignment, and program-wide precedent effects.

Reviews a counterparty's redline of a merger agreement against the initial draft and related deal materials to identify compounded risk interactions, representation issues, and asymmetric risk allocation with term-sheet deviation analysis.

Compares a clinical trial protocol against applicable regulatory requirements and pre-submission guidance to produce a gap analysis memorandum with citation-level support and remediation recommendations.

Compares a closing certificate against merger agreement pre-closing covenants and supporting documents to identify false certifications, unauthorized actions, and timing failures through a structured closing-analysis workflow.

Analyzes multiple payor contracts against a benchmark report on a contract-by-contract basis to identify rate deviations, structural adverse terms, and acquisition-relevant provisions with quantified financial impact.

Compares security and privacy policies against the HIPAA Security Rule on a policy-by-policy basis, organizing gaps by applicable safeguard category and tailoring remediation sequencing to external compliance deadlines.

Conducts an element-by-element privacy-rule gap analysis of a privacy notice and related privacy policy, addressing marketing authorization concepts, dual compliance-role obligations, and data-sharing agreement coverage gaps.

Compares a vendor cloud infrastructure proposal against internal procurement requirements and related security or compliance addenda to identify financial, technical, legal, and regulatory gaps, then organizes the differences into a negotiation-focused gap analysis.

Drafts a clinical trial agreement harmonizing sponsor and site positions on biospecimen use, publication mechanics, CRO involvement, debarment representations, and data-lock timing, with a companion memo identifying cross-document conflicts and recommended compromises.

Drafts a corporate-integrity-agreement-compliant comprehensive employee compliance training manual that identifies and resolves cross-document errors, covers whistleblower anti-retaliation, foreign anti-corruption, government pricing, and contractor obligations, with role-differentiated modules.

Drafts a CIA implementation plan and board resolution package that maps each CIA obligation to a timeline, addresses chief compliance officer qualification and independence requirements, and includes multi-period staffing and budget projections for review.

Drafts a corrective action response to an FDA warning letter that addresses each cited observation, identifies the applicable device and facility identifiers, and lays out observation-sequenced remediation steps and timelines.

Drafts a comprehensive data privacy compliance policy manual and gap analysis for a digital health company operating under overlapping healthcare-privacy obligations, addressing biometric privacy laws, consumer health data statutes, advertising SDK data sharing, and implementation deadlines.

Drafts a tailored enterprise SaaS vendor onboarding questionnaire and internal cover memo for a healthcare system, with the cover memo linking each questionnaire section to prior internal review themes in general terms and the questionnaire including a response deadline.

Drafts a tailored healthcare SaaS vendor onboarding questionnaire and internal cover memo that addresses AI/ML governance, security and incident-response enhancements, applicable consumer health-data privacy considerations, and cross-border data handling.

Drafts an FDA Prior Approval Supplement cover letter and a companion discrepancy memo that resolves cross-document conflicts on supplement classification, facility identifiers, regulatory authority citations, and user fee category.

Drafts a healthcare asset purchase agreement for an ambulatory surgery center acquisition, focusing on healthcare-specific operational transition issues, regulatory-compliance drafting, employee and lease transfer mechanics, and post-closing adjustment structure.

Drafts a definitive reverse triangular merger agreement for a healthcare transaction with healthcare-specific representations, regulatory and operational covenants, earn-out mechanics, antitrust considerations, and a companion drafting issues memorandum flagging ambiguities and buyer-side risks.

Drafts a healthcare management services agreement for a physician group engaging a management services organization, with attention to corporate practice limits, federal fraud-and-abuse constraints, fee-splitting concerns, governance mechanics, termination provisions, data rights, and related supporting materials.

Produces a fully marked-up institutional redline of a sponsor-drafted clinical trial agreement, aligning the draft to the applicable institutional research position on indemnification causation, publication rights, adverse-event reporting, protocol amendment review, and government-funding / invention-ownership considerations.

Produces a healthcare merger agreement markup commentary and issues summary chart that contextualizes each issue against the applicable negotiation playbook, incorporates cross-document references from related compliance and financing materials when they bear on the provision being analyzed, and applies a structured issue-analysis framework.

Drafts a privacy impact assessment for an AI-powered healthcare platform, focusing on algorithmic bias, inference logging, HIPAA marketing classification of automated outreach, business associate agreement secondary use scope, state health data law timing, de-identification risk, and API token security.

Drafts a comprehensive Civil Investigative Demand response with objections, interrogatory answers, and a privilege log, plus a privileged internal strategy memo analyzing preservation issues, potential whistleblower-related exposure, personal self-incrimination issues, and voluntary disclosure options.

Extract closing conditions from a merger agreement into a structured matrix, categorizing each condition by burdened party and condition type, and assessing feasibility, unusual features, and procedural interactions that may affect closing.

Extract compliance obligations from a warning letter and supporting inspection materials into a structured spreadsheet register with required columns, categorized obligations, phased timeline, and a summary/risk assessment tab.

Reviews an informed consent form against applicable informed-consent requirements, any required privacy authorization, institutional review board contact requirements, conflict-of-interest disclosure expectations, and cross-document consistency to identify missing elements, omissions, and discrepancies.

Compiles a regulatory obligation register for a pharmaceutical digital health platform launch covering healthcare privacy and security, consumer communications consent, anti-kickback and patient-assistance-program structure, substance-use-disorder confidentiality, multi-jurisdiction breach notification, professional licensure, and consumer health-data notification obligations.

Produces a structured regulatory obligations register and narrative memo for a digital health telehealth platform launch, covering data-use agreements, clinical decision support analysis, telehealth prescribing rules, biometric privacy laws, remote monitoring billing requirements, and open vendor audit findings.

Extracts and catalogs regulatory permits from healthcare acquisition diligence documents, including change-of-ownership analysis by regulatory body, operating-without-permit risk identification, facility-level compounding risk assessment, and deal-phase-organized remediation recommendations.

Extracts and catalogs reimbursement terms from a managed care payor contract and any related exhibits, focusing on methodologies, rate structures, escalation mechanics, discount provisions, audit and recoupment mechanics, value-based care terms, and termination-related payment obligations, benchmarked against general industry playbook conventions.