By Deepa ShettyLast Updated: 2 min read

Digital Product Passport (DPP) requirements are moving product information toward structured, interoperable digital data. For manufacturers, that creates a practical problem long before a DPP is published: much of the product and material information needed to build it may still live in Excel files, spreadsheets, supplier documents and disconnected systems.

The European Commission describes the DPP as a digital container for information about products, components and materials. The information required depends on the applicable product legislation, and economic operators are responsible for compiling the required data digitally and maintaining its accuracy throughout the product lifecycle. Internal Market SME

That makes the journey from supplier data → FMD → structured product data → DPP an important part of DPP readiness.

Converting an Excel file to XML can be part of that journey. But XML conversion by itself does not make product data DPP-ready.

The real challenge is making sure the data is complete, structured, validated, connected to the right product and component relationships, and capable of being maintained over time.

What Does Excel Have to Do With Digital Product Passport Readiness?

For many electronics manufacturers, product information has accumulated across spreadsheets for years.

A typical product may have:

  • Product and part numbers in an ERP system
  • BOM information in PLM
  • Material declarations from suppliers
  • RoHS and REACH declarations in compliance systems
  • FMD information in spreadsheets
  • Test reports in PDF files
  • Supplier information in email
  • Sustainability information in separate databases

The problem is not necessarily that Excel is incapable of storing useful information.

The problem is that spreadsheet data is often structured for people rather than for connected, machine-readable data exchange.

DPP implementation requires product information to follow the data structure and obligations defined by the applicable legislation. The European Commission also identifies interoperability, data exchange, data formats and machine-readable information as important parts of the DPP framework. Internal Market SME

So the question is not simply:

"How do we convert Excel to XML?"

It is:

"How do we turn the product and material data in Excel into reliable structured data that can support the applicable DPP requirements?"

Why Is Excel a Problem for Product and Material Data?

Excel can be useful for collecting and reviewing data, but problems appear when it becomes the primary system for managing product information.

Common issues include:

☐ Different suppliers use different column names

☐ Material descriptions are inconsistent

☐ Part numbers do not match across files

☐ Units are entered differently

☐ Required fields are left blank

☐ Material and substance relationships are unclear

☐ Supplier data is stored separately from the BOM

☐ Supporting evidence is stored somewhere else

☐ Older declarations remain mixed with current information

☐ Changes to components are not reflected everywhere

☐ The same product information is manually copied into multiple files

These problems become more significant when information needs to move between systems.

A spreadsheet may tell a compliance professional that a component contains a particular material. A structured data model needs to represent what that component is, which product it belongs to, what material is associated with it, what information is known about that material, and where the supporting evidence comes from.

That relationship is more important than the file extension.

What Is the Difference Between Data Formatting and Data Structure?

This distinction is critical.

Formatting describes how information is represented.

Structure describes how information relates to other information.

For example, an Excel file might contain:

Product

Component

Material

Substance

Weight

Product A

Component 001

Aluminum

Substance X

250 g

Converting that row into XML does not automatically establish whether:

  • Product A is the correct product identifier
  • Component 001 is part of the current BOM
  • Aluminum is the correct material classification
  • Substance X is correctly identified
  • 250 g refers to the component, material or substance
  • the information came from an approved supplier declaration
  • the declaration is still current

The XML can be technically valid while the underlying information is still wrong or incomplete.

This is why data quality and data modelling need to come before file conversion.

Why Does XML Matter for Machine-Readable Product Data?

XML is a structured format that can represent relationships between data elements.

Instead of treating product information as cells in a spreadsheet, structured data can represent relationships such as:

Product → Component → Material → Substance

That is useful when information needs to move between systems or be processed automatically.

The DPP framework is being developed around interoperability, structured information, machine-readable data, data exchange and related technical standards. The European Commission's DPP work now includes standards covering areas such as identifiers, interoperability, data carriers, APIs, data exchange protocols and data storage. Internal Market SME

However, XML should not be treated as a universal DPP format.

The exact technical requirements depend on the applicable product legislation, delegated acts and technical specifications.

XML is a way of structuring and exchanging data. It is not, by itself, a declaration of DPP compliance.

Does Converting Excel to XML Make Data DPP Ready?

No.

This is one of the most important distinctions manufacturers should make.

A simple conversion could look like:

Excel → XML

A more useful DPP readiness workflow looks like:

Supplier data → FMD → Validation → Product structure → BOM relationships → Evidence → Structured data → Applicable DPP requirements

The difference is significant.

A file can be converted into XML while still containing:

  • Missing information
  • Duplicate records
  • Incorrect units
  • Outdated supplier declarations
  • Inconsistent component identifiers
  • Unvalidated material information
  • Missing evidence
  • Incorrect product relationships

The European Commission states that economic operators must provide product data digitally according to the data structure and obligations defined by the relevant legislation. They are also responsible for maintaining the accuracy of DPP information throughout the product lifecycle. Internal Market SME

So conversion is a technical step inside a larger data-readiness process.

What Data Needs to Be Structured Before XML Conversion?

Before converting product information, manufacturers need to understand what the data actually represents.

For FMD-driven product information, the underlying relationships may include:

Product

↓

BOM / Assembly

↓

Component

↓

Material

↓

Substance

↓

Supporting evidence

Depending on the applicable requirement, additional information may be associated with the product, component or material.

The important point is that the manufacturer should know what each data field means and how it relates to the rest of the product.

For example:

Data area

Question to resolve

Product

Which product does this information belong to?

Component

Which component or part is involved?

Material

What material is associated with the component?

Substance

What substances are present or relevant?

Quantity

What does the reported quantity represent?

Supplier

Who provided the information?

Evidence

What document or declaration supports it?

Date

When was the information provided or validated?

Status

Is the information current and accepted?

Relationship

Where does this component sit in the product structure?

This creates a foundation that can be transformed into machine-readable data more reliably.

How Should FMD Data Be Prepared Before XML Conversion?

Full Material Disclosure can provide a useful product and material data foundation because it can connect information about components, materials and substances.

But FMD data should not simply be exported without validation.

A practical preparation process is:

1. Identify the product

Establish the product identifier and the product version or relevant product structure.

2. Establish the BOM

Connect the product to its current components and assemblies.

3. Map component information

Make sure component numbers, descriptions and supplier information are consistent.

4. Connect material information

Associate each relevant component with its material information.

5. Connect substance information

Where required, identify relevant substances and their relationships to materials.

6. Attach evidence

Connect declarations, reports or other supporting information to the relevant records.

7. Validate the data

Check completeness, consistency, units, identifiers, dates and relationships.

8. Structure the output

Only after the underlying information is reliable should manufacturers transform it into the required structured format.

This is where FMD becomes more than a compliance record.

It can become part of the product-data foundation needed for downstream digital workflows.

For a broader explanation of FMD and how material, component and substance information fits together, see the Full Material Disclosure guide.

How Do You Validate Data Before Converting It?

Validation should happen before conversion, not after.

A useful validation checklist includes:

☐ Product identifiers are consistent

☐ Current BOM information is being used

☐ Component numbers match the source system

☐ Supplier information is associated with the correct component

☐ Material information is complete

☐ Substance information is correctly associated

☐ Units are consistent

☐ Required fields are populated

☐ Supporting evidence is available

☐ Declaration dates are recorded

☐ Outdated information is identified

☐ Duplicate records are removed

☐ Data relationships are preserved

☐ Exceptions are documented

The goal is not merely to create an XML file that passes a technical parser.

The goal is to create structured product information that can be trusted.

How Does BOM Structure Fit Into the Process?

The BOM is the bridge between the product and the underlying material information.

Without that connection, manufacturers can end up with a collection of material records without a reliable understanding of where those materials exist in the product.

Consider:

Product A

→ Assembly 01

→ Component 001

→ Material X

→ Substance Y

That relationship is much more useful than simply storing:

Material X | Substance Y

The first structure provides product context.

This becomes particularly important when a manufacturer needs to determine which products are affected by a material change, supplier update or regulatory requirement.

It also supports the broader product-data chain:

Supplier → Material → Component → BOM → Product → DPP

That chain is central to turning supplier information into usable product intelligence.

What Happens When Supplier Data Comes in Different Formats?

Supplier data rarely arrives in one consistent format.

One supplier may provide:

  • Excel
  • CSV
  • XML
  • IPC declaration
  • Laboratory report
  • Technical drawing
  • PDF declaration
  • Structured portal submission

Another supplier may provide completely different information.

Trying to force every supplier into the same file format at the beginning can create unnecessary friction.

A better approach is to establish a common internal data model.

The supplier's original format can then be mapped into that model.

For example:

Supplier Excel

↓

Supplier XML

↓

IPC declaration

↓

PDF evidence

↓

Structured internal FMD record

Once the information has been normalised and validated, the manufacturer can use it for downstream compliance and product-data workflows.

This is also why supplier data collection should be treated as part of the FMD process rather than as a separate administrative activity.

See how to get FMD data without constantly chasing suppliers for a practical supplier data-collection workflow.

Can Existing FMD Data Be Reused for DPP?

Potentially, yes.

But reuse depends on the quality, scope and structure of the underlying data and the requirements applicable to the product.

The European Commission makes clear that the exact information required in a DPP depends on the relevant product legislation. Internal Market SME

That means manufacturers should avoid assuming that every FMD field will automatically become a DPP field.

Instead, think about FMD as one potential source of product and material information.

For example:

FMD

→ Material composition

→ Component information

→ Substance information

→ Supplier evidence

→ Product relationships

These records can potentially support downstream requirements where the applicable DPP rules call for relevant product, material or substance information.

The benefit is reuse.

Instead of collecting the same underlying information repeatedly for different compliance and sustainability processes, manufacturers can build a controlled product-data foundation and reuse appropriate information where requirements overlap.

What Does an Excel-to-XML Workflow Look Like?

A practical workflow can be structured into eight stages.

Stage 1: Collect

Bring together product, BOM, component, supplier and material information.

Stage 2: Normalise

Standardise identifiers, units, naming conventions and data fields.

Stage 3: Map

Connect suppliers, components, materials and substances to the correct product structure.

Stage 4: Validate

Identify missing, inconsistent, duplicate or outdated information.

Stage 5: Evidence

Connect declarations, reports and other supporting records to the relevant data.

Stage 6: Structure

Map validated information into the required data model.

Stage 7: Transform

Generate the required machine-readable representation, such as XML where applicable.

Stage 8: Maintain

Update the underlying information when products, suppliers, components, materials or requirements change.

The last stage is easy to overlook.

DPP readiness is not a one-time export exercise. The European Commission specifically places responsibility on economic operators to maintain the accuracy of DPP information throughout the product lifecycle. Internal Market SME

What Should an Excel-to-XML Readiness Checklist Include?

Before attempting to convert product data into structured output, ask:

Product structure

☐ Do we have a current product structure?

☐ Can every relevant component be connected to the correct product?

☐ Are product and component identifiers consistent?

Material data

☐ Do we know which materials are associated with each relevant component?

☐ Is the material information complete?

☐ Are material and substance relationships clear?

Supplier data

☐ Do we know which supplier provided each record?

☐ Can we identify missing supplier information?

☐ Are supplier submissions validated?

Evidence

☐ Can each important claim be traced back to supporting evidence?

☐ Are declaration dates recorded?

☐ Can outdated evidence be identified?

Data quality

☐ Are units standardised?

☐ Are duplicate records identified?

☐ Are mandatory fields complete?

☐ Are inconsistent values flagged?

Structured data

☐ Is there a defined data model?

☐ Are relationships between records preserved?

☐ Can the data be exchanged between systems?

☐ Does the output match the applicable technical requirements?

Lifecycle management

☐ Can the data be updated when the product changes?

☐ Can supplier changes be reflected?

☐ Can affected products be identified when material information changes?

This checklist helps separate data readiness from simple file conversion.

How Can Manufacturers Avoid Building Another Data Silo?

The worst outcome would be to create a new DPP spreadsheet or XML repository that becomes disconnected from the rest of the compliance process.

A better architecture connects DPP readiness to the product data manufacturers already need for compliance.

For example:

Supplier data

→ FMD

→ BOM

→ Product compliance

→ Sustainability data

→ DPP data

The same underlying product information can then support multiple workflows where the applicable requirements overlap.

This is particularly important as manufacturers manage multiple regulatory requirements at the same time.

The goal should not be to create a separate database for every regulation.

The goal should be to create a reusable, controlled product-data foundation.

How Does FMD Support the DPP Data Foundation?

FMD does not replace the DPP.

Instead, it can provide a useful source of product and material information that may support DPP preparation.

The relationship can be thought of as:

Supplier disclosures

↓

Full Material Disclosure

↓

Validated material and substance data

↓

Product and BOM relationships

↓

Structured product information

↓

Applicable DPP data

↓

DPP registration and lifecycle management

The exact DPP data requirements remain product-specific and depend on the applicable legislation and delegated acts. Internal Market SME

That distinction matters because manufacturers should prepare their data architecture now without assuming that today's spreadsheet structure or a generic XML schema represents the final requirement for every product.

How Can Regilient Support FMD and DPP Data Readiness?

Regilient can help manufacturers build the product and material data foundation behind these workflows.

The focus is not simply on converting one file into another.

It is on managing the underlying information across the lifecycle:

Collect → Validate → Connect → Assess → Document → Monitor → Update → Reuse

This can include supplier data collection, FMD management, BOM-level product intelligence, compliance assessment, supporting evidence and structured product information.

For manufacturers preparing for DPP requirements, that creates an opportunity to address the underlying data problem before the final DPP output is required.

The European Commission's DPP implementation work is already moving toward interoperable data exchange, machine-readable information and technical infrastructure for DPP registration and lifecycle management. Internal Market SME

The practical question is therefore not just whether a manufacturer can generate XML.

It is whether the manufacturer can trust the product data being put into that XML.

From Spreadsheet Data to Structured Product Intelligence

Excel to XML is not the real transformation.

The real transformation is:

Unstructured supplier information → validated FMD → connected product data → structured information → reusable DPP data

For electronics manufacturers, that means DPP preparation should start with the quality and structure of the product data already being collected.

If material information is incomplete, disconnected from the BOM or difficult to trace back to suppliers, converting it into XML will not solve the underlying problem.

Build the data foundation first. Then build the digital passport on top of it.

Recommended next step

Start by mapping your existing supplier, FMD, BOM and product information into one connected data structure. From there, identify which information can support current compliance workflows and which fields may be required for applicable DPP requirements.

Internal content path:
FMD foundation → supplier data collection → structured product data → DPP readiness.

The broader Full Material Disclosure guide explains the FMD foundation, while the DPP FMD compliance guide focuses specifically on preparing FMD data for Digital Product Passport requirements.

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From Excel Chaos to XML Confidence: Your FMD Wake-Up Call for DPP Readiness

What is the connection between Excel, XML, and Digital Product Passports?
Excel spreadsheets are often used for Full Material Disclosure (FMD) , but they aren’t machine-readable or regulatory-compliant for Digital Product Passports (DPPs). DPPs require structured, validated XML (e.g. IPC‑1752A , IEC 62474), making Excel inadequate for scalable, audit-ready compliance.
Why isn't Excel scalable for managing FMD data?
Excel lacks built-in validation for CAS numbers, has no real substance threshold enforcement, doesn’t link to live substance regulations (like SVHC or RoHS), and cannot generate interoperable formats like XML needed for regulatory submissions and DPP systems
What benefits does converting FMD data to XML provide?
XML formats (e.g. IPC‑1752A Class D, IEC 62474) enable: Substance-level data mapping with CAS numbers and concentration Automated validation checks Interoperability with systems like SCIP, IMDS, and DPP portals Version control and audit traceability
How does structured XML support Digital Product Passport readiness?
DPP requirements under EU’s Ecodesign for Sustainable Products Regulation mandate machine-readable data about material composition, compliance, recyclability, and supply chain transparency. XML format aligns with these needs and ensures compatibility with QR codes, APIs, or cloud-based DPP platforms
What are the main FMD readiness criteria for DPP compliance?
According to Regilient: Homogeneous material-level data with CAS numbers Substance flags (RoHS, SVHC, PFAS) Machine-readable XML per standard schemas Version control and audit documentation Supplier onboarding with structured formats (e.g. IPC‑1752A)
How can companies transition from Excel to XML efficiently?
Using automated compliance platforms like Regilient enables bulk FMD conversion into standardized XML formats. These tools validate data, flag regulated substances, and output interoperable files suitable for DPP systems—eliminating manual mapping and errors
Why is upgrading FMD data structure urgent now?
DPP compliance will become mandatory for many EU product categories by 2026–2027, and technical rules (delegated acts) are expected by late 2025. Companies relying on Excel now risk non-compliance, missed regulatory submissions, and loss of market access