Was your SDS rejected, questioned, or sent back for correction?

Do not assume the document only needs a quick format change. Rejections can relate to the product data, market version, classification, translation, document age, or a reviewer-specific requirement. ICSDS can review the context and help determine the right next step.

Tell Us What Happened Submit the Rejected Document

Intake

Start with the evidence

Send the current SDS, the rejection or request message, the product name, and the target market. If more technical information is required, ICSDS will identify it after the initial review.

Common categories that may require review

The document is outdated or based on old product information.

The SDS was created for a different jurisdiction or language.

Product or supplier data has changed.

Hazard communication or classification information requires review.

The reviewer is asking for information not addressed by the current document.

The issue may involve the label or another compliance workstream rather than the SDS alone.

Recommendation

What ICSDS may recommend

The correct solution could be an SDS revision, new authoring, translation, market-specific version, label review, or a broader regulatory assessment. Recommendations are made after the available information is reviewed.

Confidentiality

Confidential support

If the issue requires formulation or technical information, NDA support is available before confidential details are exchanged. You do not need to determine the regulatory cause before you contact ICSDS.

Bring the problem. We will help define the compliance path.

No long technical questionnaire. Give us the project context — we will ask for technical detail only where it matters.

NDA available before you share anything confidential.

Reviewed by in-house regulatory professionals.

Scope and timeline agreed before work begins.

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