2023 Trend: Quality 2D Codes Needed for Final Leg of FDA’s DSCSA
Printed and electronic tracking come together in the final stage of the FDA’s Drug Supply Chain Security Act (DSCSA). Unless the agency extends the November 2023 deadline, the pharmaceutical supply chain must have lot-level Electronic Product Code Information Services (EPCIS) implemented. The industrial inkjet printing industry stands to benefit from these regulations.
10 Years in the Making
The early stages of the DSCSA required human-readable information about the supply chain. Serialized tracking information established inkjet printing as the versatile solution for variable tracking information. The U.S. Congress enacted the Drug Supply Security Act in November 2013. In January 2015, they required manufacturers to begin printing lot numbers of packaging for all prescription drugs. Since then, the FDA has required other tracking information.
Required DSCSA Information
Proprietary or established name or names of the product
Strength and dosage form of the product
National Drug Code (NDC) number of the product
Number of containers
Lot number of the product
Date of the transaction
Date of the shipment if more than 24 hours after the date of the transaction
Business name and address of the person from whom ownership is being transferred
Business name and address of the person to whom ownership is being transferred
The vision for the regulations looked towards a future where both human-readable and machine-readable tracking information is required. As expected in this digital age, 2017 saw the introduction of mandates for lot-level tracking information to be transferred to supply-chain partners electronically using an advance ship notice (ASN).
What’s Changing for the Pharma Supply Chain in 2023
The DSCSA doesn’t stop at the lot level. Requirements get even more granular.
To fully protect consumers from counterfeit medications, pharma products must transfer unit-level information electronically at the handoffs in the supply chain. At this point, fully serialized traceability becomescomplete for the U.S. pharmaceutical supply chain.
Packaging units can use RFID chips or printed 2D codes to comply with interoperability. Each technology connects to a database with the required tracking information. Either way, a scanner or reader extracts the required identifiers and begins validation with the database.
Required Identifiers for Interoperability Compliance
National Drug Code (embedded in the Global Trade Item Number®, GTIN®)
How Industrial Inkjet Printing Supports DSCSA Compliance
Despite rumors of its demise, print remains very much alive.
Manufacturers place static product information onto a label and apply them to each product. Other information, such as expiration dates that change, requires inkjet printers to directly mark every bottle, container, or box with variable data.
Printing QR codes with industrial inkjet printers offer the fastest and most cost-effective solution for connecting a unit to its corresponding electronic data.
For the grand plan for the system to work, companies must print QR codes at consistently high quality.
Achieving a high-quality barcode depends on a combination of factors: printing resolution, ink and contrast, the substrate, the printing environment, and the barcode design. One or more may contribute to a barcode that won’t scan.
Inkjet inks from companies like Kao Collins optimally match the ink to the printhead technology and the pharmaceutical packaging or label material. For example, an ink that fails to dry quickly may spread, causing scanning failure. Considering the quantity of drugs produced, fast dry time also supports high-speed printing.
How the QR Code and Electronic Data Come Together
Under the DSCSA, all pharmaceutical companies in the U.S. must affix or imprint a product identifier to each package and homogenous case of a product they intend to introduce in a transaction.
Trading parties must exchange relevant and required trading transaction information and statements. This exchange should happen in a secure, electronic, and interoperable manner. The transaction information should include the product identifier at the package level.
Trading parties should be able to securely, electronically, and interoperably verify the product identifier on a sealed homogeneous case or product package. The information may be printed with industrial inkjet systems directly on a container or on a label that is applied to the label.
Trading partners must maintain a secure, electronic, and interoperable system capable of providing transaction information and statements and prompt gathering of information needed to produce the transaction information for every transaction that goes back to the manufacturer.
Products Excluded from the DSCSA
Blood or blood components intended for transfusion
Certain radioactive drugs or radioactive biological products
Certain intravenous products
Any medical gas
Homeopathic drugs marketed in accordance with applicable guidance under the FD&C Act
Drugs compounded in compliance with sections 503A or 503B of the FD&C Act (21 U.S.C. 353a or 353b).
All of the required technology is in place to support the DSCSA interoperable requirements, something that could not have been accomplished as easily before inkjet printing evolved into what it is today.