Labelling of medicines, medical devices and parapharmacy products

Consumption of pharmaceutical products and supplements is growing worldwide. Comply with the demanding regulations governing pharmaceutical labelling with our print-on-demand systems and avoid costly product recalls caused by incorrect pre-printed labels.

Precision

Print sharper text and graphics that guarantee legibility throughout the product's life cycle.

Resistance

Produce labels capable of withstanding demanding manufacturing and storage conditions for all kinds of containers and devices.

Regulatory compliance

Comply with regulations and include security codes to guarantee traceability (DataMatrix, QR codes, variable data).

Pharmacy and parapharmacy labelling applications

Digital printing helps you comply with the regulations established by the European Union and national medicines agencies, while satisfying consumers’ marketing and safety needs in the over-the-counter market.

Medicine labels

Guarantee correct pharmaceutical labelling by including the information medicines require to comply with current regulations, led by Directive 2001/83/EC, which establishes a Community code relating to medicinal products for human use, and Regulation (EU) 2016/161, which regulates the safety features designed to prevent falsification and recommends code aggregation (DataMatrix).

Medical device labelling

Medical device labelling must include information regulated by Regulation (EU) 2017/745 (MDR) on medical devices, notably specific indications such as the manufacturer or representative in the case of production outside the European Union, administration and storage conditions, and batch number in accordance with harmonised standards… Information must also be provided on aspects such as sterilisation methods or active substances of biological origin.

Medical device labelling

With our printing systems, bring your production into line with medical device labelling standards. Standardisation has been made easier with the adoption of the Unique Device Identification (UDI) system established by the European Union. UDI is regulated in Regulation (EU) 2017/745 (MDR) on medical devices and Regulation (EU) 2017/746 (IVDR) on in vitro diagnostic medical devices.

Vaccine and injectable labels

Vaccine and injectable medicine labelling must guarantee adhesion on small-volume containers and withstand sterilisation and storage conditions that can reach deep-freezing. They must also meet strict regulatory requirements set by the European Union and supervised by the European Medicines Agency (EMA).

Supplement labels

Supplement and parapharmacy labelling must reconcile marketing requirements with regulatory compliance for health protection. In the case of private-label dietary supplements sold online, it is important to ensure labels and instructions are clearly legible, even in small print — and to comply with local packaging guidelines governing the sale of such products to avoid legal problems.

Do you want to know more?
We can help you here.

Our team in Barcelona is available to guide you through your colour label printing needs and to put you in touch with a local distributor.