In a previous article , we explored how PHARMA-CODE is similar and different from other barcode types. Now we invite you to explore with us the practicalities of printing the PHARMA-CODE on your products.
With other barcode types, it is always a critical concern from the printer suppliers about validating the data structure. Certainty that the encoded information correct is an essential aspect of barcode quality with external usage (open-loop) barcodes such as GS1 and HIBC UDI. This is not a concern—or at least not the printer’s concern—with PHARMA-CODE because it serves in an internal usage (closed loop) application. Our previous article explains this in detail.
PHARMA-CODE number allocation
The sole purpose of PHARMA-CODE is to ensure that only the correct collateral information is included in a pharmaceutical package. The package itself and all relevant inserts must match. The product manufacturer allocates the PHARMA-CODE numbers for this purpose. Lookup to a database is not necessary, so a standardized numbering protocol is not required. On an assembled package, the PHARMA-CODE barcode is no longer visible. Consumers and pharmacies often pay little attention and even not aware of the existence of those PHARMA-CODE.
Two Levels of Coding
Although the number allocation is very simple, some PHARMA-CODE barcodes also use color to identify inserts and ensure they are included in package assembly. This difference could confuse and intimidate printers utilized in the automated production environment. How to make sure the printed barcodes are correct? Who is responsible for errors, why no compliance standard exists for PHARMA-CODE to control the application?
Like other barcodes, there is a PHARMA-CODE standard, but number allocation is entirely discretionary to the product manufacturer. The design file provided to a contract printer includes barcode data that is part of an internal manufacturing process. Numbering errors or discrepancies are invisible and unknown to the printer. Manage remaining concerns with a simple contractual agreement, which absolves the contractor printer or packager of responsibility for label design data, including barcodes, in the customer-supplied file.
Still, there are print quality specifications and tolerances. Verification is unconventional but important. Best practices: deploy verifying cameras when the individual medicine carton is packed, inspecting the correctness of inserts to avoid recalls. Familiar ISO print quality verification uses a red light source; barcodes are ideally black against a white substrate. To verify a multi-color PHARMA-CODE, a white light verifier is used. Special PHARMA-CODE software is also necessary.
Although PHARMA-CODE verifiers are unusual, they are commercially available. Here is one example.
Access the data sheets here.
A conventional red light verifier can be used to test and grade black-on-white PHARMA-CODE but special PHARMA-CODE software is necessary. Check with your verifier supplier for availability. We can help.
Two Levels of Verification
Verification can also include validation. This is particularly true with PHARMA-CODE, which confirms the inclusion of only the correct collateral materials in the pharmaceutical package. Verifying the barcode is the perfect time to do this. Some verifiers can perform lookup to a database. This matches the barcode to the product and assures packaging accuracy. Here too, we can help.
We are grateful for the kind and generous assistance of Dongming Wang, of Global Marketing at Laetus GmbH.
If you have questions, concerns or comments about PHARMA-CODE or any barcode issue, please contact us here.
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John helps companies resolve current barcode problems and avoid future barcode problems to stabilize and secure their supply chain and strengthen their trading partner relationships.