Skip to main content

CODITECT STANDARDS

Product Requirements Document Template & Framework

For AI-Driven Autonomous Development in Regulated Industries


Version: 1.0
Classification: Template
Last Updated: [DATE]


Table of Contents

  1. Document Control
  2. Intent Understanding Framework
  3. Disambiguation Framework
  4. Requirements Structure
  5. Compliance Framework
  6. AI Agent Interpretation Guide
  7. Glossary
  8. Appendices

1. Document Control

Purpose of This Section

Document Control establishes traceability, accountability, and version management critical for regulated industry compliance (FDA 21 CFR Part 11, HIPAA, SOC2). For AI agentic systems, this section provides metadata that enables agents to understand document authority, currency, and stakeholder context.

Document Information

FieldValue
Document Title[PROJECT NAME] - Product Requirements Document
Document IDPRD-[PROJECT-CODE]-[VERSION]
StatusDraft | In Review | Approved | Deprecated
ClassificationInternal | Confidential | Regulated
Compliance ScopeFDA 21 CFR Part 11 | HIPAA | SOC2 | None
Created Date[YYYY-MM-DD]
Last Updated[YYYY-MM-DD]
Author[Name, Role]
Approver[Name, Role]

Version History

VersionDateAuthorChange Summary
0.1[Date][Name]Initial draft
0.2[Date][Name][Description of changes]
1.0[Date][Name]Approved for development

🤖 WHY THIS MATTERS FOR AI AGENTS

AI agents must reference version history to understand requirement evolution. When agents encounter conflicting information, version timestamps resolve precedence. Classification level informs what information can be shared or processed. Compliance scope triggers specific validation requirements in generated artifacts.

❌ NOT Needed in This Section

  • Detailed change logs at line level (use version control systems)
  • Meeting minutes or discussion threads (maintain separately)
  • Approval signatures for drafts (only required for approved versions)
  • Distribution lists (managed externally)

2. Intent Understanding Framework

⚠️ CRITICAL SECTION

This section is the cornerstone of AI agent comprehension. Without clear intent documentation, AI agents cannot distinguish between what the user SAID versus what they MEANT. The Intent Understanding Framework provides the cognitive scaffolding necessary for autonomous systems to make decisions aligned with stakeholder goals.

2.1 The Intent Hierarchy

User requirements exist at multiple levels of abstraction. AI agents must understand all levels to make appropriate decisions during autonomous development.

LevelDefinitionExampleAI Agent Use
Strategic IntentThe ultimate business outcome desiredReduce medication errors in hospital settingsGuides architectural decisions and trade-off resolution
Tactical IntentThe approach chosen to achieve strategic goalsBuild an AI-powered drug interaction checkerInforms technology selection and integration patterns
Operational IntentSpecific capabilities requiredAlert clinicians when dangerous combinations are prescribedDrives feature implementation and acceptance criteria
Functional IntentDetailed behaviors and interactionsDisplay red warning banner with severity scoreDetermines UI/UX implementation specifics

2.2 Why Intent Understanding is Critical

The Interpretation Gap

Every requirement statement contains implicit assumptions. When a stakeholder says "the system should be fast," they have a mental model of acceptable performance. Without explicit intent documentation, AI agents must guess:

❌ WITHOUT Intent Documentation✅ WITH Intent Documentation
"Fast" could mean:"Fast" means:
• Sub-second response• P95 latency < 200ms
• Faster than current system• Context: Clinical workflow
• Real-time streaming• Rationale: Match clinician attention span
• Just "not slow"• Constraint: Must beat 3-second current state
Agent GUESSES and may be wrongAgent KNOWS and implements correctly

The Cost of Misunderstanding

In regulated industries, misinterpreted intent creates compliance risk. An AI agent that implements a "notification" as an email when the intent was a real-time alert could:

  1. Delay critical clinical information (patient safety impact)
  2. Fail FDA audit trail requirements (regulatory violation)
  3. Require costly rework after compliance review (budget impact)
  4. Erode stakeholder trust in autonomous development (adoption risk)

2.3 Capturing Intent: The Five Ws + How

For each requirement, document:

ElementQuestionPurpose for AI Agents
WHOWho benefits? Who performs the action?Identifies personas, roles, and permission boundaries
WHATWhat capability is needed?Defines the functional requirement
WHYWhy is this needed? What problem does it solve?Enables agents to resolve ambiguity by returning to first principles
WHENWhen is this needed? Under what conditions?Establishes temporal and conditional logic
WHEREWhere in the system/workflow does this occur?Determines integration points and context boundaries
HOWHow should it work? What are the constraints?Provides implementation guidance and quality attributes

2.4 Intent Documentation Template

┌─────────────────────────────────────────────────────────────────┐
│ INTENT BLOCK │
├─────────────────────────────────────────────────────────────────┤
│ Requirement ID: [REQ-XXX] │
│ Statement: [The system shall...] │
│ │
│ Strategic Context: [How this supports business goals] │
│ User Story: As a [role], I want [capability] │
│ so that [benefit] │
│ │
│ Success Looks Like: [Observable outcome when intent satisfied] │
│ Failure Looks Like: [Observable outcome when NOT satisfied] │
│ │
│ Implicit Assumptions: [What the stakeholder takes for granted] │
│ Boundary Conditions: [Edge cases and limits] │
│ Anti-Requirements: [What this explicitly is NOT] │
└─────────────────────────────────────────────────────────────────┘

2.5 Intent Survival Verification

🚨 CRITICAL FINDING (Empirically Validated)

Research shows that 20-30% of requirements are silently dropped during AI planning phases—not because they're unclear, but because planning modes act as "filters" that normalize inputs. Intent that doesn't survive translation is intent that won't get built.

The Silent Loss Problem

Intent Document → PRD → Plan → Build
100% 80% 56% 45% ← TYPICAL LOSS PATTERN

With Verification Loops:
Intent Document → PRD → Plan → Build
100% 95% 90% 85% ← CODITECT TARGET

Mandatory Verification Pattern

After each planning phase, AI agents MUST:

  1. Extract all requirements from source document (PRD)
  2. Extract all planned items from generated plan
  3. Diff to produce FALLOUT LIST (PRD items not in plan)
  4. Score coverage percentage
  5. Iterate if coverage < 95%
  6. Escalate if coverage < 80% after 3 iterations

Intent Survival Metrics

MetricTargetAction if Below
PRD Capture Rate≥95%Revise PRD generation prompt
Plan Coverage Rate≥95%Run verification loop
Build Implementation Rate≥90%Review build execution
Total Survival Rate≥85%Full pipeline audit

Fallout List Template

┌─────────────────────────────────────────────────────────────────┐
│ FALLOUT REPORT │
├─────────────────────────────────────────────────────────────────┤
│ Planning Pass: #[N] │
│ Coverage: [X]% │
│ Status: ✅ PASS | ⚠️ ITERATE | 🚨 ESCALATE │
├─────────────────────────────────────────────────────────────────┤
│ MISSING REQUIREMENTS: │
│ │
│ | Req ID | Description | PRD Section | Severity | │
│ |--------|-------------|-------------|----------| │
│ | [ID] | [Desc] | [Section] | [H/M/L] | │
│ │
│ RECOMMENDED ACTION: [Iterate/Escalate/Accept] │
└─────────────────────────────────────────────────────────────────┘

❌ NOT Needed in Intent Documentation

  • Implementation details (belongs in Technical Design Documents)
  • Test cases (derived from intent but documented separately)
  • Schedule or timeline information (belongs in project plans)
  • Resource allocation (separate concern)

3. Disambiguation Framework

Purpose

Ambiguity is inherent in human communication. For AI agents to function autonomously, ambiguity must be systematically identified and resolved. This section provides the framework for transforming ambiguous requirements into actionable specifications.

3.1 Types of Ambiguity

Ambiguity TypeDefinitionExampleResolution Strategy
LexicalWords with multiple meanings"Table" - furniture or data structure?Define domain-specific glossary
SyntacticSentence structure allows multiple interpretations"Users can edit documents with permissions"Restructure using formal patterns
SemanticMeaning unclear from context"System should be user-friendly"Define measurable criteria
ReferentialUnclear what pronouns or references point to"It should validate before that"Explicit noun references
PragmaticIntent unclear despite clear words"Consider implementing caching"Clarify must-have vs nice-to-have
OmissionMissing information assumed known"Standard security practices"Enumerate all requirements explicitly

3.2 The Disambiguation Process

Step 1: Ambiguity Detection

AI agents must be trained to recognize ambiguity indicators:

Red Flag WordsProblematic PatternsMissing Elements
appropriate, adequatePassive voice constructionsNo units of measure
easy, simple, intuitiveMissing actors/subjectsNo frequency specified
fast, quick, responsiveCompound requirementsNo error handling
user-friendly, modernNegation chainsNo boundary conditions
flexible, robustConditional cascadesNo security context
etc., and so on, similarImplied comparisonsNo user role specified
some, several, manyOpen-ended listsNo success criteria
usually, typically, oftenUndefined acronymsNo compliance mapping

Step 2: Disambiguation Questions

For each ambiguity detected, generate targeted questions:

┌─────────────────────────────────────────────────────────────────┐
│ DISAMBIGUATION TEMPLATE │
├─────────────────────────────────────────────────────────────────┤
│ Original Statement: │
│ "The system should respond quickly to user actions." │
│ │
│ Ambiguity Identified: │
│ "quickly" - undefined performance metric │
│ │
│ Disambiguation Questions: │
│ 1. What is the maximum acceptable response time in ms? │
│ 2. Does this apply to all actions or specific operations? │
│ 3. Under what load conditions must this be maintained? │
│ 4. What is the current baseline we are improving upon? │
│ 5. Are there regulatory requirements for response time? │
│ │
│ Disambiguated Statement: │
│ "The system SHALL respond to drug interaction checks within │
│ 200ms (P95) under normal load (100 concurrent users) and │
│ within 500ms under peak load (500 concurrent users), │
│ measured from request submission to result display, to meet │
│ clinical workflow requirements per CPOE guidelines." │
└─────────────────────────────────────────────────────────────────┘

Step 3: The Disambiguation Decision Tree

AMBIGUITY DETECTED


┌──────────────────┐
│ Is compliance- │─── YES ──▶ ALWAYS ESCALATE TO HUMAN
│ related? │
└────────┬─────────┘
│ NO

┌──────────────────┐
│ Score > 0.6? │─── YES ──▶ ESCALATE TO HUMAN
└────────┬─────────┘
│ NO

┌──────────────────┐
│ Context │─── NO ───▶ ESCALATE TO HUMAN
│ sufficient? │
└────────┬─────────┘
│ YES

RESOLVE + DOCUMENT

3.3 Ambiguity Scoring

AI agents should calculate ambiguity scores to determine escalation need:

Score RangeInterpretationAction
0.0 - 0.2Clear requirementImplement autonomously
0.2 - 0.4Minor ambiguityImplement with documentation of interpretation
0.4 - 0.6Significant ambiguityPropose interpretation for human review
0.6 - 0.8High ambiguityRequest clarification before implementation
0.8 - 1.0Critical ambiguityBlock implementation until resolved

⚠️ AGENT AUTONOMY LEVELS

  • Level 1 (Auto-resolve): Clear glossary match or explicit context - agent resolves independently
  • Level 2 (Resolve + Flag): Reasonable inference but some uncertainty - agent resolves and flags for review
  • Level 3 (Escalate): High ambiguity or compliance impact - agent MUST NOT proceed without human input

In regulated industries, default to Level 3 for any requirement with compliance implications.

3.4 Resolution Documentation

Every disambiguation creates an audit trail:

FieldPurposeExample
Ambiguity IDUnique identifier for trackingAMB-PRD-001
Original TextVerbatim requirement as received"System should be fast"
Ambiguity TypeClassification from taxonomySemantic - undefined metric
Stakeholder ConsultedWho provided clarificationDr. Smith, Clinical Informatics
Date ResolvedTimestamp for audit trail2025-01-15
ResolutionClear, testable statement"Response time < 200ms P95"
RationaleWhy this resolution was chosenClinical workflow studies show >300ms disrupts clinician flow
Compliance ImpactRegulatory implicationsFDA UDI response time guidelines

❌ NOT Part of Disambiguation

  • Arguing with stakeholders about what they meant (document their clarification)
  • Making assumptions without documentation (all inferences must be recorded)
  • Changing stakeholder intent to match easier implementation (disambiguation clarifies, does not alter intent)

4. Requirements Structure

Purpose

A well-structured requirements framework enables AI agents to understand scope, priority, and dependencies. Structure provides the semantic scaffolding necessary for autonomous decision-making during development.

4.1 Executive Summary

What This Section Is

A concise overview (250-500 words) that captures the essence of the product for any reader. This section should stand alone and provide enough context for stakeholders to understand the product vision without reading the entire document.

Why It Matters for AI Agents

The Executive Summary serves as the "north star" for agent decision-making. When agents face ambiguous choices, they reference this section to align decisions with overall product direction.

Template

[PRODUCT NAME] is a [product category] designed for [target users] in the [industry/domain] sector. The primary problem it solves is [problem statement]. Key differentiators include [2-3 unique value propositions]. Success will be measured by [key metrics]. The product must comply with [regulatory requirements]. Initial release is targeted for [timeline] with [scope description].

❌ NOT Needed in Executive Summary

  • Technical architecture details
  • Feature-level specifications
  • Implementation approaches
  • Team structure or resource plans
  • Detailed timelines or Gantt charts

4.2 Problem Statement

What This Section Is

A clear articulation of the problem or opportunity that justifies the product. This section answers "Why does this product need to exist?" and "What happens if we do nothing?"

Template

┌─────────────────────────────────────────────────────────────────┐
│ PROBLEM STATEMENT │
├─────────────────────────────────────────────────────────────────┤
│ Current State: [Describe how things work today] │
│ Pain Points: [Specific problems, quantified] │
│ Impact: [Business/user consequences] │
│ Root Cause: [Why the problem exists] │
│ Desired Future State: [What success looks like] │
│ Constraints: [Boundaries that must be respected] │
└─────────────────────────────────────────────────────────────────┘

Why It Matters for AI Agents

The Problem Statement provides the "Why" that grounds all implementation decisions. When agents must choose between approaches, they evaluate options against how well they address the stated problem.

4.3 Functional Requirements

What This Section Is

Detailed descriptions of what the system must do. Functional requirements describe capabilities, features, and behaviors from the user perspective.

Requirement Format

ElementDescriptionExample
IDUnique identifier with hierarchyFR-AUTH-001
TitleBrief descriptive nameUser Authentication
PriorityMoSCoW classificationMUST
DescriptionClear statement using SHALL/SHOULD/MAYThe system SHALL authenticate users via SAML 2.0 SSO
RationaleWhy this requirement existsEnterprise security policy requires centralized identity
Acceptance CriteriaTestable conditions for successAC1: Valid SAML assertion grants access; AC2: Invalid assertion shows error
DependenciesRelated requirementsFR-SEC-001, NFR-PERF-003
Compliance MappingRegulatory requirements addressedHIPAA 164.312(d)

Priority Definitions (MoSCoW)

PriorityDefinitionAgent Interpretation
MUSTCritical for release; non-negotiableImplement first; block release if incomplete
SHOULDImportant but workarounds existImplement if time permits; can defer with documented trade-off
COULDDesirable enhancementImplement only after MUST/SHOULD complete
WON'TExplicitly out of scope for this releaseDo NOT implement; document as future consideration

❌ NOT Needed in Functional Requirements

  • How to implement the feature (belongs in TDD)
  • UI mockups or wireframes (reference design documents)
  • Database schemas (technical specification)
  • API contracts (interface documents)
  • Test scripts (QA documentation)

4.4 Non-Functional Requirements

What This Section Is

Quality attributes that constrain how the system operates. Non-functional requirements (NFRs) define performance, security, scalability, and other "-ility" characteristics.

NFR Categories

CategoryDescriptionTypical Metrics
PerformanceSpeed and responsivenessLatency (ms), throughput (req/sec), page load time
ScalabilityHandling growthMax concurrent users, data volume limits
AvailabilityUptime and reliabilitySLA percentage, MTTR, MTBF
SecurityProtection requirementsEncryption standards, auth protocols, audit logging
ComplianceRegulatory requirementsFDA 21 CFR Part 11, HIPAA, SOC2 controls
MaintainabilityEase of changeCode coverage, documentation requirements
UsabilityUser experienceTask completion time, error rate, satisfaction score
AccessibilityInclusive designWCAG level, assistive tech compatibility

🚨 CRITICAL FOR REGULATED INDUSTRIES

In FDA-regulated environments, NFRs around audit trails, electronic signatures, and data integrity are not optional. AI agents must treat compliance NFRs as MUST priorities regardless of business priority. Failure to implement compliance requirements correctly can result in regulatory action.

4.5 User Stories and Personas

What This Section Is

Narrative descriptions of user needs and goals. Personas provide archetypal users; user stories describe specific interactions in their voice.

Persona Template

┌─────────────────────────────────────────────────────────────────┐
│ PERSONA TEMPLATE │
├─────────────────────────────────────────────────────────────────┤
│ Name: [Persona name - memorable, archetypal] │
│ Role: [Job title and responsibilities] │
│ Demographics: [Experience level, tech comfort, etc.] │
│ Goals: [What they want to achieve] │
│ Pain Points: [Current frustrations] │
│ Context of Use: [When, where, how they interact] │
│ Success Criteria: [How they measure value] │
└─────────────────────────────────────────────────────────────────┘

User Story Format

As a [persona], I want [capability], so that [benefit].

Why It Matters for AI Agents

Personas enable agents to evaluate decisions from the user perspective. When facing implementation choices, agents can simulate: "Would Dr. Sarah (busy ER physician) be able to use this effectively during a crisis?"

4.6 Constraints and Assumptions

What This Section Is

Documented limitations and underlying assumptions that bound the solution space. These prevent scope creep and surface hidden expectations.

TypeDefinitionExample
Technical ConstraintTechnology limitations imposedMust integrate with existing Oracle database
Business ConstraintOrganizational limitationsBudget capped at $500K
Regulatory ConstraintCompliance mandatesMust complete FDA 510(k) clearance
Timeline ConstraintSchedule requirementsMVP by Q2 to meet HIMSS deadline
AssumptionBelieved truths not yet validatedUsers have reliable internet access

⚠️ ASSUMPTION RISK

Every assumption carries risk. AI agents should flag assumptions that, if wrong, would invalidate requirements. High-risk assumptions need validation plans.

4.7 Dependencies and Integrations

What This Section Is

External systems, services, and data sources that the product relies upon or must interface with.

Dependency TypeDescriptionRisk Consideration
UpstreamSystems that feed data to this productAvailability, data quality, schema changes
DownstreamSystems that consume this product's dataContract compatibility, failure propagation
PeerSystems that operate alongsideResource contention, coordination
InfrastructurePlatform dependenciesVersion compatibility, deprecation
VendorThird-party servicesSLA, continuity, security

5. Compliance Framework

🚨 REGULATORY CONTEXT

Coditect operates in regulated industries including healthcare, fintech, and life sciences. Every requirement must be evaluated against applicable regulatory frameworks. AI agents MUST NOT make autonomous decisions that could compromise compliance.

5.1 FDA 21 CFR Part 11

What This Covers

FDA regulations governing electronic records and electronic signatures. Applicable when building software for clinical trials, medical devices, or pharmaceutical manufacturing.

Key Requirements for AI Agents

RequirementDescriptionAgent Implementation Guidance
Audit TrailSystem must maintain secure, computer-generated, time-stamped audit trailsEvery data modification must log: who, what, when, why
Electronic SignaturesSignatures must be linked to records and non-repudiableImplement cryptographic binding of signature to content
Access ControlsSystem access limited to authorized individualsRole-based access with principle of least privilege
Record IntegrityRecords must be accurate, complete, and protectedImplement checksums, prevent unauthorized modification
ValidationSystems must be validated for intended useMaintain validation documentation, change control

5.2 HIPAA Security Rule

What This Covers

Regulations governing Protected Health Information (PHI) in healthcare settings. Applicable when building software that creates, receives, maintains, or transmits PHI.

Safeguard Categories

SafeguardRequirementsAgent Implementation Guidance
AdministrativePolicies, procedures, risk analysisDocument security policies in requirements
PhysicalFacility access, workstation securityInfrastructure requirements for deployment
TechnicalAccess control, encryption, integritySpecific NFRs for authentication, encryption

5.3 SOC 2 Controls

What This Covers

Trust service criteria for service organizations. Applicable when building SaaS products that handle customer data.

Trust Service Criteria

CriteriaFocus AreaTypical Requirements
SecurityProtection against unauthorized accessFirewalls, encryption, access controls
AvailabilitySystem uptime and accessibilitySLAs, redundancy, disaster recovery
Processing IntegrityComplete, valid, accurate processingInput validation, error handling, reconciliation
ConfidentialityProtection of confidential infoData classification, encryption at rest
PrivacyCollection and use of personal infoConsent, data minimization, retention limits

5.4 Compliance Mapping Template

Every requirement with compliance implications must include:

┌─────────────────────────────────────────────────────────────────┐
│ COMPLIANCE MAPPING TEMPLATE │
├─────────────────────────────────────────────────────────────────┤
│ Requirement ID: [ID] │
│ Applicable Regulations: [FDA Part 11 | HIPAA | SOC2 | Other] │
│ Specific Controls: [Control references, e.g., HIPAA │
│ 164.312(a)(1)] │
│ Evidence Required: [What must be documented for audit] │
│ Validation Approach: [How compliance will be verified] │
│ Risk if Non-Compliant: [Regulatory consequence] │
└─────────────────────────────────────────────────────────────────┘

6. AI Agent Interpretation Guide

Purpose

This section provides explicit guidance for AI agentic systems interpreting this PRD. It establishes decision boundaries, escalation triggers, and interpretation rules that enable autonomous operation while maintaining safety and quality.

6.1 Decision Authority Matrix

Decision TypeAgent AuthorityEscalation TriggerExample
Implementation DetailFULL - Agent decides autonomouslyNone unless conflicts with requirementsChoice of algorithm for sorting
Minor Requirement InterpretationCONDITIONAL - Agent decides with documentationAmbiguity score > 0.3Exact error message wording
Feature Trade-offLIMITED - Agent proposes, human approvesAlways escalateReducing scope to meet deadline
Compliance DecisionNONE - Human decision requiredAlways escalateHow to implement audit trail
Architecture ChangeNONE - Human decision requiredAlways escalateChanging database technology

6.2 Interpretation Rules

Rule 1: Explicit Over Implicit

When requirements conflict between explicit statements and implicit assumptions, explicit statements always win. Document the conflict and resolution.

Rule 2: Safety Over Features

When a feature implementation could compromise security, privacy, or compliance, choose the safer implementation even if it reduces functionality. Escalate for human review.

Rule 3: User Intent Over Literal Text

When literal interpretation of a requirement produces an outcome that clearly contradicts user intent (as documented), flag the discrepancy and propose resolution aligned with intent.

Rule 4: Compliance is Non-Negotiable

Never implement shortcuts that could compromise regulatory compliance. When in doubt, escalate. Regulatory consequences can include fines, market removal, and criminal liability.

Rule 5: Document Everything

Every interpretation, assumption, and decision must be documented. Future agents and humans will need to understand why decisions were made.

6.3 Planning Verification Protocol

⚠️ EMPIRICALLY VALIDATED REQUIREMENT

AI planning modes drop 20-30% of requirements silently. This is not a bug—it's how planning filters work. Coditect agents MUST implement verification loops.

Three-Pass Verification Pattern

PASS 1: Initial Planning
├── Generate plan from PRD
├── Extract planned items
├── Compare against PRD requirements
├── Generate Fallout List #1
└── Coverage typically: 70-80%

PASS 2: Recovery Planning
├── Append Fallout List #1 to context
├── Regenerate plan sections
├── Compare against PRD requirements
├── Generate Fallout List #2
└── Coverage typically: 85-92%

PASS 3: Final Verification
├── Append Fallout List #2 to context
├── Final plan refinement
├── Compare against PRD requirements
├── Generate Final Fallout Report
└── Coverage target: ≥95%

Agent Implementation Requirement

async def verified_planning(prd: PRDDocument, max_passes: int = 3) -> VerifiedPlan:
"""
Planning with mandatory verification loops.

CRITICAL: Do NOT skip verification. Silent losses are
unacceptable in regulated industries.
"""
coverage = 0.0
fallout_lists = []

for pass_num in range(1, max_passes + 1):
# Generate or refine plan
plan = await generate_plan(prd, fallout_lists)

# MANDATORY: Compare against source
coverage, fallout = await verify_against_prd(plan, prd)
fallout_lists.append(fallout)

# Log for audit trail
log_verification_pass(pass_num, coverage, fallout)

if coverage >= 0.95:
break

if coverage < 0.80:
raise EscalationRequired(
f"Coverage {coverage:.1%} below threshold after {max_passes} passes"
)

return VerifiedPlan(plan, coverage, fallout_lists)

6.4 Glossary Precedence

When interpreting terms, consult in order:

  1. Project-specific glossary (highest precedence)
  2. Domain-specific standards (e.g., HL7 FHIR for healthcare)
  3. Industry-standard definitions (e.g., ISO, IEEE)
  4. Common technical usage (lowest precedence)

⚠️ MULTI-AGENT TOKEN MULTIPLICATION

When operating in multi-agent orchestration (15x multiplier), budget requirements interpretation carefully. Complex disambiguation processes consume significant tokens. For high-ambiguity requirements, request human clarification rather than exhaustive autonomous analysis.


7. Glossary

Purpose

The glossary eliminates lexical ambiguity by defining terms as used in this document. AI agents should consult this glossary before inferring term meanings.

Domain Terms

TermDefinitionContext
Audit TrailSecure, timestamped log of system events and data changesFDA Part 11 compliance
Electronic SignatureComputer-generated means of authenticationRegulatory; not digital signature
PHIProtected Health Information - individually identifiable health dataHIPAA context
SAMLSecurity Assertion Markup Language - SSO protocolAuthentication
StakeholderPerson with interest in or influence over the productAnyone affected by decisions

[Add project-specific terms as needed]

Requirement Language (RFC 2119)

TermMeaning
SHALLAbsolute requirement
SHALL NOTAbsolute prohibition
SHOULDRecommended but not mandatory
SHOULD NOTNot recommended but not prohibited
MAYOptional
MUSTEquivalent to SHALL

8. Appendices

Appendix A: Referenced Documents

[List related documents: Technical Design Document, Architecture Decision Records, etc.]

Appendix B: Change Request Process

[Document process for requesting changes to this PRD]

Appendix C: Stakeholder Contacts

[Contact information for requirement clarification]

Appendix D: Compliance Checklists

[Regulatory compliance verification checklists]


Document Metadata

document:
type: PRD_TEMPLATE
version: 1.1 # Updated with empirical findings
standard: CODITECT_STANDARDS
compliance_scope:
- FDA_21_CFR_PART_11
- HIPAA
- SOC2
ai_agent_guidance:
disambiguation_threshold: 0.6
escalation_required:
- compliance_decisions
- architecture_changes
- feature_tradeoffs
- coverage_below_80_percent # NEW
autonomous_allowed:
- implementation_details
- minor_interpretations_with_documentation
# NEW: Intent Survival Requirements
intent_verification:
enabled: true
min_coverage: 0.95
max_planning_passes: 3
fallout_list_required: true
escalate_if_below: 0.80
token_awareness:
single_agent_multiplier: 4
multi_agent_multiplier: 15
optimization_priority: verification_loops # Changed from disambiguation_caching
# NEW: Empirical Validation Reference
validated_by:
experiment: "9 Apps Experiment"
key_finding: "Planning modes drop 20-30% of requirements silently"
mitigation: "3-pass verification recovers 90%+ of losses"

CODITECT STANDARDS | PRD Template v1.1
For AI-Driven Autonomous Development in Regulated Industries
Updated with empirical validation from intent survival research