Indonesia’s pharmaceutical track and trace system has evolved significantly, beginning with a traceability project in 2018 and progressing toward ambitious goals set for 2025–2027.
The Indonesian National Agency of Drug and Food Control (BPOM) has taken proactive steps to enhance a secure and sustainable pharmaceutical supply chain. In 2022, BPOM replaced the 2018 law on serialization and traceability with an updated regulation. In 2023, BPOM launched the e-Labeling Pilot Project, reinforcing its commitment to future-ready pharmaceutical oversight.
This document outlines the labeling process, including traceability, serialization, aggregation requirements, and noted exceptions.
All pharmaceutical manufacturers in Indonesia must use a 2D Data Matrix barcode to enable product tracking and tracing. The barcodes must comply with GS1 standards, as mandated by Regulation No. 22/2022, effective from October 5, 2022.
Manufacturers can either:
There are two types of barcodes:
Implementation Deadlines
The Identification Barcode is a QR code used to:
Applicability
Products not requiring serialization should only include an Identification Barcode. These include:
Note: Barcodes must be obtained through electronic Marketing Authorization (MA) approval and include:
The NIE (Nomor Izin Edar) is a product license number issued by BPOM. It indicates the product’s origin (domestic or imported) and provides access to product data in the BPOM’s “Cek Produk” database.
Serialization uses the Authentication Barcode, which is a 2D Data Matrix containing a unique identifier.
Applicability
Serialization is required for:
Barcode Data Requirements
Note: To request barcodes via the Track and Trace app, businesses must submit:
Aggregation is mandatory and must follow GS1 standards using the SSCC (Serial Shipping Container Code).
The following products are exempt from barcode requirements:
CONCLUSION: In today’s evolving global landscape, traceability is more than a regulatory requirement — it’s a strategic imperative. Our advanced solutions help your organization achieve seamless compliance, end-to-end transparency, and the highest standards of pharmaceutical safety.
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