@cregis-dev/cckit 0.3.0 → 0.4.1

package/templates/bmad/bmm/workflows/2-plan-workflows/create-prd/steps-v/step-v-08-domain-compliance-validation.md

@@ -1,243 +1,243 @@
----
-name: 'step-v-08-domain-compliance-validation'
-description: 'Domain Compliance Validation - Validate domain-specific requirements are present for high-complexity domains'
-
-# File references (ONLY variables used in this step)
-nextStepFile: './step-v-09-project-type-validation.md'
-prdFile: '{prd_file_path}'
-prdFrontmatter: '{prd_frontmatter}'
-validationReportPath: '{validation_report_path}'
-domainComplexityData: '../data/domain-complexity.csv'
----
-
-# Step 8: Domain Compliance Validation
-
-## STEP GOAL:
-
-Validate domain-specific requirements are present for high-complexity domains (Healthcare, Fintech, GovTech, etc.), ensuring regulatory and compliance requirements are properly documented.
-
-## MANDATORY EXECUTION RULES (READ FIRST):
-
-### Universal Rules:
-
-- 🛑 NEVER generate content without user input
-- 📖 CRITICAL: Read the complete step file before taking any action
-- 🔄 CRITICAL: When loading next step with 'C', ensure entire file is read
-- 📋 YOU ARE A FACILITATOR, not a content generator
-- ✅ YOU MUST ALWAYS SPEAK OUTPUT In your Agent communication style with the config `{communication_language}`
-
-### Role Reinforcement:
-
-- ✅ You are a Validation Architect and Quality Assurance Specialist
-- ✅ If you already have been given communication or persona patterns, continue to use those while playing this new role
-- ✅ We engage in systematic validation, not collaborative dialogue
-- ✅ You bring domain expertise and compliance knowledge
-- ✅ This step runs autonomously - no user input needed
-
-### Step-Specific Rules:
-
-- 🎯 Focus ONLY on domain-specific compliance requirements
-- 🚫 FORBIDDEN to validate other aspects in this step
-- 💬 Approach: Conditional validation based on domain classification
-- 🚪 This is a validation sequence step - auto-proceeds when complete
-
-## EXECUTION PROTOCOLS:
-
-- 🎯 Check classification.domain from PRD frontmatter
-- 💬 If low complexity (general): Skip detailed checks
-- 🎯 If high complexity: Validate required special sections
-- 💾 Append compliance findings to validation report
-- 📖 Display "Proceeding to next check..." and load next step
-- 🚫 FORBIDDEN to pause or request user input
-
-## CONTEXT BOUNDARIES:
-
-- Available context: PRD file with frontmatter classification, validation report
-- Focus: Domain compliance only (conditional on domain complexity)
-- Limits: Don't validate other aspects, conditional execution
-- Dependencies: Steps 2-7 completed - format and requirements validation done
-
-## MANDATORY SEQUENCE
-
-**CRITICAL:** Follow this sequence exactly. Do not skip, reorder, or improvise unless user explicitly requests a change.
-
-### 1. Load Domain Complexity Data
-
-Load and read the complete file at:
-`{domainComplexityData}` (../data/domain-complexity.csv)
-
-This CSV contains:
-- Domain classifications and complexity levels (high/medium/low)
-- Required special sections for each domain
-- Key concerns and requirements for regulated industries
-
-Internalize this data - it drives which domains require special compliance sections.
-
-### 2. Extract Domain Classification
-
-From PRD frontmatter, extract:
-- `classification.domain` - what domain is this PRD for?
-
-**If no domain classification found:**
-Treat as "general" (low complexity) and proceed to step 4
-
-### 2. Determine Domain Complexity
-
-**Low complexity domains (skip detailed checks):**
-- General
-- Consumer apps (standard e-commerce, social, productivity)
-- Content websites
-- Business tools (standard)
-
-**High complexity domains (require special sections):**
-- Healthcare / Healthtech
-- Fintech / Financial services
-- GovTech / Public sector
-- EdTech (educational records, accredited courses)
-- Legal tech
-- Other regulated domains
-
-### 3. For High-Complexity Domains: Validate Required Special Sections
-
-**Attempt subprocess validation:**
-
-"Perform domain compliance validation for {domain}:
-
-Based on {domain} requirements, check PRD for:
-
-**Healthcare:**
-- Clinical Requirements section
-- Regulatory Pathway (FDA, HIPAA, etc.)
-- Safety Measures
-- HIPAA Compliance (data privacy, security)
-- Patient safety considerations
-
-**Fintech:**
-- Compliance Matrix (SOC2, PCI-DSS, GDPR, etc.)
-- Security Architecture
-- Audit Requirements
-- Fraud Prevention measures
-- Financial transaction handling
-
-**GovTech:**
-- Accessibility Standards (WCAG 2.1 AA, Section 508)
-- Procurement Compliance
-- Security Clearance requirements
-- Data residency requirements
-
-**Other regulated domains:**
-- Check for domain-specific regulatory sections
-- Compliance requirements
-- Special considerations
-
-For each required section:
-- Is it present in PRD?
-- Is it adequately documented?
-- Note any gaps
-
-Return compliance matrix with presence/adequacy assessment."
-
-**Graceful degradation (if no Task tool):**
-- Manually check for required sections based on domain
-- List present sections and missing sections
-- Assess adequacy of documentation
-
-### 5. For Low-Complexity Domains: Skip Detailed Checks
-
-Append to validation report:
-```markdown
-## Domain Compliance Validation
-
-**Domain:** {domain}
-**Complexity:** Low (general/standard)
-**Assessment:** N/A - No special domain compliance requirements
-
-**Note:** This PRD is for a standard domain without regulatory compliance requirements.
-```
-
-Display: "**Domain Compliance Validation Skipped**
-
-Domain: {domain} (low complexity)
-
-**Proceeding to next validation check...**"
-
-Without delay, read fully and follow: {nextStepFile}
-
-### 6. Report Compliance Findings (High-Complexity Domains)
-
-Append to validation report:
-
-```markdown
-## Domain Compliance Validation
-
-**Domain:** {domain}
-**Complexity:** High (regulated)
-
-### Required Special Sections
-
-**{Section 1 Name}:** [Present/Missing/Adequate]
-{If missing or inadequate: Note specific gaps}
-
-**{Section 2 Name}:** [Present/Missing/Adequate]
-{If missing or inadequate: Note specific gaps}
-
-[Continue for all required sections]
-
-### Compliance Matrix
-
-| Requirement | Status | Notes |
-|-------------|--------|-------|
-| {Requirement 1} | [Met/Partial/Missing] | {Notes} |
-| {Requirement 2} | [Met/Partial/Missing] | {Notes} |
-[... continue for all requirements]
-
-### Summary
-
-**Required Sections Present:** {count}/{total}
-**Compliance Gaps:** {count}
-
-**Severity:** [Critical if missing regulatory sections, Warning if incomplete, Pass if complete]
-
-**Recommendation:**
-[If Critical] "PRD is missing required domain-specific compliance sections. These are essential for {domain} products."
-[If Warning] "Some domain compliance sections are incomplete. Strengthen documentation for full compliance."
-[If Pass] "All required domain compliance sections are present and adequately documented."
-```
-
-### 7. Display Progress and Auto-Proceed
-
-Display: "**Domain Compliance Validation Complete**
-
-Domain: {domain} ({complexity})
-Compliance Status: {status}
-
-**Proceeding to next validation check...**"
-
-Without delay, read fully and follow: {nextStepFile} (step-v-09-project-type-validation.md)
-
----
-
-## 🚨 SYSTEM SUCCESS/FAILURE METRICS
-
-### ✅ SUCCESS:
-
-- Domain classification extracted correctly
-- Complexity assessed appropriately
-- Low complexity domains: Skipped with clear "N/A" documentation
-- High complexity domains: All required sections checked
-- Compliance matrix built with status for each requirement
-- Severity assessed correctly
-- Findings reported to validation report
-- Auto-proceeds to next validation step
-- Subprocess attempted with graceful degradation
-
-### ❌ SYSTEM FAILURE:
-
-- Not checking domain classification before proceeding
-- Performing detailed checks on low complexity domains
-- For high complexity: missing required section checks
-- Not building compliance matrix
-- Not reporting findings to validation report
-- Not auto-proceeding
-
-**Master Rule:** Domain compliance is conditional. High-complexity domains require special sections - low complexity domains skip these checks.
+---
+name: 'step-v-08-domain-compliance-validation'
+description: 'Domain Compliance Validation - Validate domain-specific requirements are present for high-complexity domains'
+
+# File references (ONLY variables used in this step)
+nextStepFile: './step-v-09-project-type-validation.md'
+prdFile: '{prd_file_path}'
+prdFrontmatter: '{prd_frontmatter}'
+validationReportPath: '{validation_report_path}'
+domainComplexityData: '../data/domain-complexity.csv'
+---
+
+# Step 8: Domain Compliance Validation
+
+## STEP GOAL:
+
+Validate domain-specific requirements are present for high-complexity domains (Healthcare, Fintech, GovTech, etc.), ensuring regulatory and compliance requirements are properly documented.
+
+## MANDATORY EXECUTION RULES (READ FIRST):
+
+### Universal Rules:
+
+- 🛑 NEVER generate content without user input
+- 📖 CRITICAL: Read the complete step file before taking any action
+- 🔄 CRITICAL: When loading next step with 'C', ensure entire file is read
+- 📋 YOU ARE A FACILITATOR, not a content generator
+- ✅ YOU MUST ALWAYS SPEAK OUTPUT In your Agent communication style with the config `{communication_language}`
+
+### Role Reinforcement:
+
+- ✅ You are a Validation Architect and Quality Assurance Specialist
+- ✅ If you already have been given communication or persona patterns, continue to use those while playing this new role
+- ✅ We engage in systematic validation, not collaborative dialogue
+- ✅ You bring domain expertise and compliance knowledge
+- ✅ This step runs autonomously - no user input needed
+
+### Step-Specific Rules:
+
+- 🎯 Focus ONLY on domain-specific compliance requirements
+- 🚫 FORBIDDEN to validate other aspects in this step
+- 💬 Approach: Conditional validation based on domain classification
+- 🚪 This is a validation sequence step - auto-proceeds when complete
+
+## EXECUTION PROTOCOLS:
+
+- 🎯 Check classification.domain from PRD frontmatter
+- 💬 If low complexity (general): Skip detailed checks
+- 🎯 If high complexity: Validate required special sections
+- 💾 Append compliance findings to validation report
+- 📖 Display "Proceeding to next check..." and load next step
+- 🚫 FORBIDDEN to pause or request user input
+
+## CONTEXT BOUNDARIES:
+
+- Available context: PRD file with frontmatter classification, validation report
+- Focus: Domain compliance only (conditional on domain complexity)
+- Limits: Don't validate other aspects, conditional execution
+- Dependencies: Steps 2-7 completed - format and requirements validation done
+
+## MANDATORY SEQUENCE
+
+**CRITICAL:** Follow this sequence exactly. Do not skip, reorder, or improvise unless user explicitly requests a change.
+
+### 1. Load Domain Complexity Data
+
+Load and read the complete file at:
+`{domainComplexityData}` (../data/domain-complexity.csv)
+
+This CSV contains:
+- Domain classifications and complexity levels (high/medium/low)
+- Required special sections for each domain
+- Key concerns and requirements for regulated industries
+
+Internalize this data - it drives which domains require special compliance sections.
+
+### 2. Extract Domain Classification
+
+From PRD frontmatter, extract:
+- `classification.domain` - what domain is this PRD for?
+
+**If no domain classification found:**
+Treat as "general" (low complexity) and proceed to step 4
+
+### 2. Determine Domain Complexity
+
+**Low complexity domains (skip detailed checks):**
+- General
+- Consumer apps (standard e-commerce, social, productivity)
+- Content websites
+- Business tools (standard)
+
+**High complexity domains (require special sections):**
+- Healthcare / Healthtech
+- Fintech / Financial services
+- GovTech / Public sector
+- EdTech (educational records, accredited courses)
+- Legal tech
+- Other regulated domains
+
+### 3. For High-Complexity Domains: Validate Required Special Sections
+
+**Attempt subprocess validation:**
+
+"Perform domain compliance validation for {domain}:
+
+Based on {domain} requirements, check PRD for:
+
+**Healthcare:**
+- Clinical Requirements section
+- Regulatory Pathway (FDA, HIPAA, etc.)
+- Safety Measures
+- HIPAA Compliance (data privacy, security)
+- Patient safety considerations
+
+**Fintech:**
+- Compliance Matrix (SOC2, PCI-DSS, GDPR, etc.)
+- Security Architecture
+- Audit Requirements
+- Fraud Prevention measures
+- Financial transaction handling
+
+**GovTech:**
+- Accessibility Standards (WCAG 2.1 AA, Section 508)
+- Procurement Compliance
+- Security Clearance requirements
+- Data residency requirements
+
+**Other regulated domains:**
+- Check for domain-specific regulatory sections
+- Compliance requirements
+- Special considerations
+
+For each required section:
+- Is it present in PRD?
+- Is it adequately documented?
+- Note any gaps
+
+Return compliance matrix with presence/adequacy assessment."
+
+**Graceful degradation (if no Task tool):**
+- Manually check for required sections based on domain
+- List present sections and missing sections
+- Assess adequacy of documentation
+
+### 5. For Low-Complexity Domains: Skip Detailed Checks
+
+Append to validation report:
+```markdown
+## Domain Compliance Validation
+
+**Domain:** {domain}
+**Complexity:** Low (general/standard)
+**Assessment:** N/A - No special domain compliance requirements
+
+**Note:** This PRD is for a standard domain without regulatory compliance requirements.
+```
+
+Display: "**Domain Compliance Validation Skipped**
+
+Domain: {domain} (low complexity)
+
+**Proceeding to next validation check...**"
+
+Without delay, read fully and follow: {nextStepFile}
+
+### 6. Report Compliance Findings (High-Complexity Domains)
+
+Append to validation report:
+
+```markdown
+## Domain Compliance Validation
+
+**Domain:** {domain}
+**Complexity:** High (regulated)
+
+### Required Special Sections
+
+**{Section 1 Name}:** [Present/Missing/Adequate]
+{If missing or inadequate: Note specific gaps}
+
+**{Section 2 Name}:** [Present/Missing/Adequate]
+{If missing or inadequate: Note specific gaps}
+
+[Continue for all required sections]
+
+### Compliance Matrix
+
+| Requirement | Status | Notes |
+|-------------|--------|-------|
+| {Requirement 1} | [Met/Partial/Missing] | {Notes} |
+| {Requirement 2} | [Met/Partial/Missing] | {Notes} |
+[... continue for all requirements]
+
+### Summary
+
+**Required Sections Present:** {count}/{total}
+**Compliance Gaps:** {count}
+
+**Severity:** [Critical if missing regulatory sections, Warning if incomplete, Pass if complete]
+
+**Recommendation:**
+[If Critical] "PRD is missing required domain-specific compliance sections. These are essential for {domain} products."
+[If Warning] "Some domain compliance sections are incomplete. Strengthen documentation for full compliance."
+[If Pass] "All required domain compliance sections are present and adequately documented."
+```
+
+### 7. Display Progress and Auto-Proceed
+
+Display: "**Domain Compliance Validation Complete**
+
+Domain: {domain} ({complexity})
+Compliance Status: {status}
+
+**Proceeding to next validation check...**"
+
+Without delay, read fully and follow: {nextStepFile} (step-v-09-project-type-validation.md)
+
+---
+
+## 🚨 SYSTEM SUCCESS/FAILURE METRICS
+
+### ✅ SUCCESS:
+
+- Domain classification extracted correctly
+- Complexity assessed appropriately
+- Low complexity domains: Skipped with clear "N/A" documentation
+- High complexity domains: All required sections checked
+- Compliance matrix built with status for each requirement
+- Severity assessed correctly
+- Findings reported to validation report
+- Auto-proceeds to next validation step
+- Subprocess attempted with graceful degradation
+
+### ❌ SYSTEM FAILURE:
+
+- Not checking domain classification before proceeding
+- Performing detailed checks on low complexity domains
+- For high complexity: missing required section checks
+- Not building compliance matrix
+- Not reporting findings to validation report
+- Not auto-proceeding
+
+**Master Rule:** Domain compliance is conditional. High-complexity domains require special sections - low complexity domains skip these checks.