SFDA Post-Market Surveillance 2025 | Saudi Food Registration

Learn how SFDA monitors food product safety in Saudi Arabia after approval. Stay compliant with post-market surveillance rules | Saudi Food Registration.

6/16/20252 min read

Saudi Food Registration logo overlay with inspector hands checking food product labels
Saudi Food Registration logo overlay with inspector hands checking food product labels

How SFDA Monitors Post-Market Surveillance for Food Products in Saudi Arabia (2025 Guide)

Getting SFDA registration for your food product is only the first step. Once your product enters the Saudi market, it becomes part of SFDA’s post-market surveillance (PMS) system — an ongoing process that monitors safety, compliance, and quality even after approval.

In this guide, we explain exactly how SFDA monitors food products after they’re registered, and what companies need to know to stay compliant in 2025.

What Is Post-Market Surveillance (PMS)?

Post-market surveillance refers to the SFDA’s regulatory activities after your product is on the market.

Its primary goals are to:

  • Ensure ongoing safety and product quality

  • Detect any safety risks that may arise over time

  • Confirm labeling and claims remain accurate

  • Verify imported products match approved specifications

  • Enforce recalls or corrective actions if problems occur

Why Does SFDA Conduct Post-Market Surveillance?

PMS helps SFDA maintain full control over public health. Even fully approved products can develop safety concerns due to:

  • Changes in ingredient sourcing

  • Storage or transportation issues

  • Undeclared allergens

  • Fraudulent or counterfeit products

  • Unauthorized label modifications

SFDA actively monitors products to catch these issues before they impact consumers.

How Does SFDA Monitor Products After Approval?

1️⃣ Routine Market Inspections

SFDA inspectors visit warehouses, distribution centers, ports, and retail outlets to:

  • Review product labels and packaging

  • Confirm Arabic language compliance

  • Verify production and expiry dates

  • Cross-check imported goods against registered dossiers

2️⃣ Sampling and Laboratory Testing

SFDA may pull random product samples to test for:

  • Microbiological contamination

  • Heavy metals or chemical residues

  • Undeclared ingredients or allergens

  • Shelf life verification

3️⃣ Barcode and Traceability Checks

Using registered barcodes and SFDA systems, inspectors verify that:

  • Barcodes match registered products

  • Traceability systems work for recalls or safety alerts

4️⃣ Import Shipment Audits

SFDA may inspect shipments during customs clearance to ensure:

  • Packaging matches registration details

  • SASO compliance for packaging and labeling

  • Correct documentation accompanies imports

5️⃣ Complaint and Incident Investigations

If a consumer, retailer, or distributor files a complaint, SFDA may:

  • Launch targeted inspections

  • Request additional testing data

  • Demand corrective action from the manufacturer

What Happens If Non-Compliance Is Found?

If SFDA identifies violations, they may:

  • Issue warning letters

  • Impose fines or penalties

  • Temporarily suspend imports

  • Mandate product recalls

  • Suspend or cancel SFDA registration

Early corrective actions often reduce the severity of penalties.

How Can Companies Stay Compliant Post-Approval?

  • Maintain full batch traceability

  • Keep accurate and updated import records

  • Review all label changes with regulatory experts before implementation

  • Perform ongoing internal audits on safety and stability

  • Stay informed of new SFDA regulations and circulars

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Compliance Doesn’t End at Approval

Post-market surveillance is not a one-time event — it’s a continuous responsibility.

Companies that proactively monitor their products and maintain full transparency with SFDA reduce their risk and protect both consumers and their brand.

Need help maintaining SFDA compliance after approval?
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