Key Capabilities
- 1SVHC screening and threshold checks at material/part/BOM level
- 2Supplier declaration & test evidence intake with version control
- 3SCIP field mapping (identifiers, SVHC info, EU article category, safe-use)
- 4Complex object (assembly) tree builder with reuse across products
- 5Submission exports/API payloads and audit-ready document packs
How It Works

Identify in-scope articles by screening against the Candidate List.

Collect & validate supplier evidence; flag gaps for closure.

Populate required SCIP fields and validations.

Model complex objects and reuse sub-assemblies.

Export submission files and archive evidence for audits.
Free Resource: SCIP Compliance Guide
Learn how to prepare and submit SCIP notifications under the EU Waste Framework Directive (WFD). This guide explains SVHC identification, IUCLID dossier preparation, supply-chain data collection, and the steps required to submit and maintain SCIP database notifications.
Download E-Book
Operational Benefits

Cut manual effort with automated validations and reusable datasets

Reduce submission errors with field checks and required metadata

Maintain an auditable evidence trail across suppliers and parts

Scale submissions across product portfolios without rework
SCIP Implementation & Advisory Services
Pair the platform with experts who operationalize SCIP: faster onboarding, cleaner data, and smoother submissions.

Implementation (4–8 weeks)
- Data model & field configuration
- Supplier request templates & workflows
- BOM tree modeling and reuse patterns
- Team training (ops, quality, sourcing)
Outcome:
Live environment; first submission dataset generated.

Advisory (Quarterly)
- Applicability & prioritization rules
- Evidence QA & gap closure plans
- Submission readiness reviews
- Executive risk/readiness updates
Outcome:
Fewer surprises; faster responses to requests.

Managed Service (MSP)
- Ongoing supplier outreach & validation
- Dataset maintenance and change monitoring
- Submission support and archive management
- SLA: initial triage in 2 business days
Outcome:
Stable compliance ops without adding headcount.
SCIP: Manual vs Software
| Process Area | Manual (Spreadsheets) | Software (Regilient) |
|---|---|---|
| SVHC Screening | Ad-hoc checks, inconsistent thresholds | Rules engine with threshold logic |
| Complex Objects | Rebuilt per product, error-prone | Reusable BOM/assembly trees |
| Field Validation | Copy/paste, missing metadata | Structured fields & required checks |
| Submissions | One-off files, no lineage | Export templates, APIs, full audit trail |
SCIP Scope & Roles (High-Level)
| Role | Typical Actions (examples) |
|---|---|
| Producer / Assembler | Screen parts for SVHCs, submit SCIP for articles and complex objects, maintain updates. |
| Importer | Ensure imported articles are assessed and submissions made as required. |
| Distributor | Pass information and maintain records where applicable. |
Always verify current applicability, data elements, and any portal/process changes in official guidance.
SCIP Compliance Checklist
- Confirm articles with SVHCs above threshold
- Collect and validate supplier evidence
- Build/maintain complex object trees
- Populate required SCIP fields
- Export & submit; archive documentation
FAQs for SCIP (WFD) Compliance Software
Useful Waste Framework Directive Compliance Resources
Related Compliance Solutions
Achieve SCIP Compliance Efficiently
Automate screening, standardize datasets, and keep documentation audit-ready with Regilient.




