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Industries · Pharmaceuticals

CDSCO-first serialisation & authentication

Meet India’s track & trace expectations for Schedule H medicines with GS1 identifiers, signed scan events, and submission schemas our regulatory team validates before you go live.

Why CDSCO changes the game

Unit-level traceability is no longer a packaging exercise — it is a continuous data programme. Regulators expect consistent GTIN, batch, expiry, and serial encoding, with provable custody across CMOs, 3PLs, and distributors.

Pre-mapped data elements

CDSCO-required fields are modelled into Ratifye so commissioning and shipping events emit regulator-aligned payloads.

Crypto layer on every unit

Copied barcodes fail verification — reducing substandard and falsified medicine risk in secondary markets.

Recall in minutes

Identify affected serials across the network and notify partners with signed evidence for audits.

Export markets

Extend the same serial foundation toward DSCSA and EU FMD reporting with guidance from Ratifye specialists.

Typical go-live

Most teams connect GS1 master data, turn on line commissioning, deploy scanners with the Ratifye SDK, and run parallel verification for two weeks before switching production reporting. Timelines compress when master data is already clean.

Explore the platform

Start with serialization and track & trace, then layer authentication at warehouses and pharmacies.