Creating and Publishing an EPD
A step-by-step guide to developing, verifying, and publishing your Environmental Product Declaration.
Prerequisites:
Creating and Publishing an EPD
Creating an Environmental Product Declaration requires careful planning, rigorous data collection, and third-party verification. This lesson walks through the complete process from initial planning to published EPD.
Overview: The EPD Development Timeline
A typical EPD project follows this timeline:
| Phase | Duration | Activities |
|---|---|---|
| Planning | 2-4 weeks | Select program operator, identify PCR, scope project |
| LCA Development | 8-16 weeks | Data collection, modeling, calculations |
| EPD Preparation | 2-4 weeks | Format results, prepare documentation |
| Verification | 4-8 weeks | Third-party review, revisions |
| Publication | 1-2 weeks | Registration, public posting |
Total timeline: 4-8 months depending on complexity and data availability.
Phase 1: Planning and Preparation
Step 1.1: Define Your Goals
Before starting, clarify why you're creating an EPD:
- Market access: Required by customers or regulations?
- Competitive differentiation: Demonstrating environmental leadership?
- Internal improvement: Using LCA to identify reduction opportunities?
- Regulatory compliance: Meeting Buy Clean or similar requirements?
Your goals influence decisions about scope, program operator, and investment level.
Step 1.2: Select a Program Operator
Consider these factors when choosing:
| Factor | Questions to Ask |
|---|---|
| Market recognition | Will my customers accept EPDs from this operator? |
| PCR availability | Do they have a PCR for my product category? |
| Geographic relevance | Are they recognized in my target markets? |
| Cost | What are registration and renewal fees? |
| Support | What guidance and templates do they provide? |
| Timeline | What is their typical verification turnaround? |
Step 1.3: Identify the Applicable PCR
Search the program operator's PCR library for your product category:
- Find PCRs covering your product type
- Verify the PCR is current (not expired)
- Review scope definitions to confirm your product fits
- Note any sub-categories or product groups
If no PCR exists, discuss options with the program operator:
- Use general program rules
- Initiate PCR development
- Wait for planned PCRs
Step 1.4: Assemble Your Team
EPD projects typically require:
Internal resources:
- Product/process expert (knows manufacturing details)
- Data coordinator (gathers production data)
- Project manager (coordinates activities)
- Management sponsor (approves scope and budget)
External resources:
- LCA consultant (if conducting LCA externally)
- Verification body (required for third-party verification)
Even if you conduct the LCA internally, consider engaging an experienced EPD consultant to review your work before verification. This can prevent costly revisions later.
Phase 2: Conducting the LCA
The LCA must comply with ISO 14040/14044 and the applicable PCR.
Step 2.1: Define Goal and Scope
Document per ISO requirements:
Goal:
- Intended application (support EPD development)
- Reasons for carrying out the study
- Intended audience (B2B customers, specifiers, etc.)
- Comparability intentions
Scope:
- Product system description
- Functional unit (as specified in PCR)
- System boundary (modules included per PCR)
- Allocation procedures
- Cut-off criteria
- Impact categories
- Data quality requirements
Step 2.2: Collect Life Cycle Inventory Data
This is typically the most time-consuming phase.
Foreground data (specific to your product):
| Data Type | Sources |
|---|---|
| Material inputs | Bills of materials, purchasing records |
| Energy consumption | Utility bills, meter readings |
| Direct emissions | Emissions reports, measurements |
| Waste generation | Waste manifests, hauling records |
| Water use | Utility bills, flow meters |
| Transport | Shipping records, logistics data |
Background data (generic supply chain data):
| Data Type | Sources |
|---|---|
| Raw material production | LCI databases (ecoinvent, GaBi, etc.) |
| Electricity grids | Regional grid data from databases |
| Transportation | Database transport processes |
| Waste treatment | Generic treatment processes |
Step 2.3: Build the LCA Model
Using your LCA software:
- Create the product system per your scope
- Enter foreground data for your processes
- Link to background database processes
- Configure allocation methods per PCR requirements
- Verify mass and energy balances
Step 2.4: Calculate Impact Assessment
Run LCIA using the method(s) specified in the PCR:
- Select required impact categories
- Calculate results for each life cycle module (A1, A2, A3, etc.)
- Generate contribution analyses
- Identify and investigate any anomalies
Step 2.5: Interpret Results
Before finalizing:
- Completeness check: Are all significant flows included?
- Sensitivity analysis: How do key assumptions affect results?
- Consistency check: Were methods applied uniformly?
- Contribution analysis: Do hotspots make sense?
Document interpretation per ISO 14044 Section 4.5.
PCRs often specify data quality requirements (age, geographic scope, technology coverage). Ensure your data meets these requirements and document where it doesn't.
Phase 3: Preparing the EPD Document
Step 3.1: Use the Program Operator's Template
Most operators provide templates ensuring compliance:
- EPD International: Template generator tool
- UL Solutions: EPD template files
- IBU: Structured reporting format
Step 3.2: Complete Required Sections
Product information:
- Manufacturer name and contact
- Product name, description, and identification
- Manufacturing location(s)
- Declared unit and reference service life
LCA information:
- LCA practitioner and date
- Database(s) and software used
- System boundary diagram
- Scenarios and assumptions
Environmental performance:
- Impact indicators by life cycle module
- Resource use indicators
- Waste and output flows
- Additional environmental information
Quality and verification:
- Data quality assessment
- Verification details
- Validity period
Step 3.3: Prepare Supporting Documentation
Verification requires additional documentation:
LCA report: Comprehensive technical report meeting ISO 14044 requirements, typically including:
- Detailed methodology description
- Complete inventory tables
- Full LCIA results
- Data quality assessment
- Interpretation and conclusions
Background documentation:
- Data collection forms
- Calculation spreadsheets
- Database references
- Correspondence on methodology decisions
Phase 4: Third-Party Verification
Step 4.1: Select a Verifier
Verifiers must be approved by your program operator. Select based on:
- Accreditation status
- Experience with your product category
- Availability and timeline
- Cost
Step 4.2: Understand the Verification Process
Verification includes:
Document review:
- EPD content and completeness
- LCA methodology compliance
- PCR conformance
- Data quality adequacy
Calculation verification:
- LCA model review
- Spot-check calculations
- Database appropriateness
- LCIA method application
Optional site visit:
- Verify data sources
- Understand processes
- Confirm representativeness
Step 4.3: Respond to Verifier Comments
Verifiers typically issue:
- Minor comments: Documentation clarifications, formatting
- Major comments: Methodological issues, data concerns
- Non-conformances: Must be resolved before approval
Respond systematically to each comment with:
- Actions taken
- Justification if no change made
- Evidence of corrections
Step 4.4: Obtain Verification Statement
After satisfactory resolution:
- Verifier issues verification statement
- Statement includes verifier details and conformance declaration
- Statement is incorporated into EPD
Phase 5: Publication and Maintenance
Step 5.1: Register with Program Operator
Submit to program operator:
- Final EPD document
- Verification statement
- Registration fee
- Any required declarations
Step 5.2: Publication
The program operator will:
- Review submission for completeness
- Assign registration number
- Publish on their EPD library
- Issue publication confirmation
Your EPD is now publicly available and can be shared with customers.
Step 5.3: Ongoing Maintenance
EPDs require ongoing attention:
Validity period: Typically 5 years, but may require annual confirmation that data remains representative.
Updates required when:
- Production process changes significantly
- Impact results change more than threshold (often 10%)
- PCR is updated with new requirements
- Errors are identified
Renewal process:
- Update LCA with current data
- Re-verify if changes exceed thresholds
- Submit renewal to program operator
Cost Considerations
EPD projects vary widely in cost:
| Component | Range | Factors Affecting Cost |
|---|---|---|
| LCA development | $15,000-80,000+ | Complexity, data availability, consultant rates |
| Verification | $3,000-15,000 | Verifier rates, number of products, site visits |
| Registration | $1,000-5,000 | Program operator fees, multi-product discounts |
| Annual maintenance | $500-2,000 | Program operator requirements |
Total first-year cost: $20,000-100,000+ depending on complexity.
Cost reduction strategies:
- Develop EPDs for product families, not individual products
- Use industry-average EPDs where available
- Conduct LCA internally if you have expertise
- Participate in industry EPD programs with shared costs
Key Takeaways
- EPD development typically takes 4-8 months from start to publication
- Select program operator and PCR early—they determine methodology requirements
- Data collection is usually the most time-intensive phase
- Build relationships with verifiers who understand your product category
- Budget for ongoing maintenance, not just initial development
Practice Checklist
Before starting your EPD project, verify:
- Clear goal and business case defined
- Program operator selected
- Applicable PCR identified and reviewed
- Internal resources assigned
- Budget approved
- Timeline realistic for data collection needs
- Verifier identified and available
What's Next?
The final lesson in this track provides a comprehensive resource list of program operators, PCR databases, and support organizations for your EPD development work.
Further Reading
- ISO 14025:2006 Environmental labels and declarations — Type III environmental declarations
- EPD International Guidance Documents
- UL Solutions EPD Guide