As a professional in the field of pharmaceutical packaging, you understand the importance of quality printing. That's where Print on Pharmaceutical Packaging comes in - providing you with expert advice and solutions for printing on blister packaging. Pharmaceutical and medical device manufactures are legally required to follow certain product coding and marking regulations. Governing bodies such as the U.S. Food and Drug Administration (FDA) develop and administer these mandates.
The FDA requires multi-use medical devices to be marked with a permanent Unique Device Identifier (UDI). Our Thermal Inkjet (TIJ) RNJet H1 system provides the most reliable method for UDI direct marking. Unlike temporary labels that tear or degrade, the H1 prints high-resolution 2D DataMatrix codes and serial numbers directly onto devices, ensuring traceability lasts for the product's entire lifecycle through reprocessing and sterilization.
Packaging and labeling errors, such as missing lot numbers or label mix-ups, account for a significant percentage of FDA recalls. The RNJet H1 offers a superior way to code drug products, cases, and cartons. By ensuring absolute legibility of drug names on blister packs and providing robust batch information, our systems prevent non-conformances. Our specialized inks are long-lasting and impervious to the handling required in pharmaceutical supply chains.

Our specialized inks and high-speed printers are designed for pharma industry.
Pharmacy labels must clearly show key details like the patient’s name, medication name and strength, dosage instructions, prescribing doctor, and expiration date. Labels should be easy to read, accurate, and compliant with local laws and safety guidelines to ensure proper use and avoid medication errors.
Track and Trace in pharma refers to the process of monitoring a drug’s journey through the supply chain - from manufacturing to the end user. It uses unique identifiers (like barcodes or serial numbers) to verify, trace, and record each product’s movement. This helps prevent counterfeiting, ensures safety, and complies with regulations like the DSCSA (U.S.) or FMD (EU).
Serialization in pharma is the process of assigning a unique serial number to each saleable unit of a drug product. This code, often combined with product ID, batch number, and expiration date, helps track the product through the supply chain. It’s a key part of anti-counterfeiting efforts and regulatory compliance, ensuring drug authenticity and patient safety.
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