You’ve committed to Full Material Disclosure (FMD). Good. That means you’re thinking beyond checkboxes and aiming for real transparency. But let’s be honest — collecting FMDs from your supply chain isn’t exactly plug-and-play.
At Acquis, we’ve helped companies handle thousands of FMDs, and Irrespective of industry, the same core challenges pop up again and again. Lets explore the top FMD headaches — and what you can actually do to fix them.
This is where it all starts — and often stalls. Suppliers submit partial declarations, leave out key materials, or skip CAS numbers like they’re optional.
The common culprits of Full Material Disclosure:
Fix it: Set expectations early. Require a minimum completeness level (we suggest 90%+) and always follow up for missing CAS numbers. For recurring gaps, consider mapping from SDS or engineering drawings as a starting point.
Sometimes you get the data, but it’s just… wrong. CAS numbers that don’t match the substance name, percentages that don’t add up, or a total part weight that seems to defy physics.
What common error do we see a lot in Full Material Disclosure
Fix it: Use automated validation tools that flag discrepancies on import. Manual review is not scalable. Trust us, you don’t want to VLOOKUP your way through 500 parts.
Here’s where incomplete or inaccurate FMDs start to hurt. Substances that exceed legal thresholds. Exemptions that aren’t justified. Supplier declarations that haven’t been updated since 2019.
Watch out for these using Full Material Disclosure for compliance:
Restricted substances (e.g., RoHS, REACH SCIP, Prop 65, POPs)
Fix it: Automate cross-checking against live substance lists. If your system can’t flag a newly added SVHC, you’re flying blind. Require suppliers to confirm exemption applicability in writing (no guesswork allowed).
Here’s a fun one: 20 suppliers, 20 formats. Some send PDFs, some Excel, others outdated XML. You end up stitching things together like a regulatory jigsaw puzzle.
Big problems:
Fix it: Ask for data in structured formats (IPC 1752A, IMDS, IEC 62474), and use a platform like Acquis Compliance Tool to bring everything into one system-readable format. Standardization is how you scale.
Data without documentation is just storytelling.
Often missing:
Fix it: Build documentation requirements into your data request process. Store it alongside the FMDs — not in a separate email chain from six months ago.
Even if the FMD is perfect, it can still fall apart at the BOM level. We’ve seen it all — materials mapped to the wrong components, duplication, and worse, no linkage at all.
Typical issues:
Fix it: Integrate your engineering BOM with your compliance system. Run alignment checks regularly. And please — don’t manage this manually in spreadsheets.
This is the elephant in the room. Even with all your systems and standards in place, you still need one thing: your supplier to cooperate.
Challenges include:
Fix it:
Fix it: Set a schedule for annual or bi-annual FMD refreshes. And don’t treat process chemicals as optional — they're often where the risks hide.
FMD is not a one-and-done exercise. It’s a continuous process that gets better (and more useful) the more you refine it. The key isn’t perfection — it’s visibility. If you can see what’s in your product, you can manage risk, reduce cost, and stay one step ahead of compliance chaos.
Next Up: Why FMD is a Smart Business Investment (Even If You’re Not in Compliance)
We’ll learn the ROI behind FMD — from cost savings and risk reduction to smoother customer audits and ESG reporting wins. Want that post in your inbox early? You know what to do.
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