Detailed roadmap phases according to 𝐓𝐫𝐚𝐜𝐤_𝐚𝐧𝐝_𝐭𝐫𝐚𝐜𝐞_𝐬𝐭𝐚𝐧𝐝𝐚𝐫𝐝𝐬_𝐅𝐂_𝐯𝟐 which announced by Pharmacy and Poisons Board last year
𝐏𝐡𝐚𝐬𝐞 𝟏 – 𝐁𝐚𝐬𝐢𝐜 𝐁𝐚𝐭𝐜𝐡 𝐓𝐫𝐚𝐜𝐞𝐚𝐛𝐢𝐥𝐢𝐭𝐲
Track products at batch level using GTIN + batch recording.
Simple data exchange (Excel/paper). Optional central batch database.
𝐏𝐡𝐚𝐬𝐞 𝟐 – 𝐄𝐥𝐞𝐜𝐭𝐫𝐨𝐧𝐢𝐜 𝐁𝐚𝐭𝐜𝐡 𝐒𝐲𝐬𝐭𝐞𝐦
Mandatory electronic data exchange (EDI).
Central repository managed by regulator.
Standard location codes (GLN).
𝐏𝐡𝐚𝐬𝐞 𝟑 – 𝐏𝐢𝐥𝐨𝐭 𝐒𝐞𝐫𝐢𝐚𝐥𝐢𝐳𝐚𝐭𝐢𝐨𝐧 (𝐇𝐢𝐠𝐡-𝐑𝐢𝐬𝐤 𝐏𝐫𝐨𝐝𝐮𝐜𝐭𝐬)
Unit-level serial numbers + GS1 DataMatrix.
Serialized data repository + pilot verification system.
𝐏𝐡𝐚𝐬𝐞 𝟒 – 𝐅𝐮𝐥𝐥 𝐍𝐚𝐭𝐢𝐨𝐧𝐚𝐥 𝐒𝐞𝐫𝐢𝐚𝐥𝐢𝐳𝐚𝐭𝐢𝐨𝐧
Mandatory unit-level serialization for all regulated products.
Nationwide verification system + healthcare integration.
𝐏𝐨𝐢𝐧𝐭𝐬 𝐭𝐨 𝐛𝐞 𝐡𝐢𝐠𝐡𝐥𝐢𝐠𝐡𝐭𝐞𝐝 𝐟𝐫𝐨𝐦 𝐦𝐲 𝐫𝐞𝐚𝐝𝐢𝐧𝐠 𝐭𝐨 𝐭𝐡𝐞 𝐬𝐭𝐚𝐧𝐝𝐚𝐫𝐝𝐬
For Gs1 Datamatrix labelling
All blister packs and sachets (Primary packaging) sold directly as such to consumers: unique identifier must be printed directly on the blister pack or sachet
All bottle or vial products (Primary packaging) sold directly as such to consumers: unique identifier must be printed directly on bottle or vial
Aggregation of serialized secondary packages into a serialized(sGTIN) tertiary package (case) and then onto a pallet with SSCC. (See Pic below)
Patients can verify their dispensed medicines using a mobile app linked to the central database.