Pharmaceutical labels
Label production tailored to pharmaceutical requirements
Nordvalls develops and produces pharmaceutical labels and labelling solutions for pharmaceutical companies, contract manufacturers and development partners (CMOs/CDMOs), medical device companies, pharmacies, laboratories and healthcare providers. With extensive experience in label production and a production environment aligned with GMP principles, we follow rigorous, documented processes throughout the product lifecycle.
From material selection and prepress to production, quality control and delivery, we ensure that every stage is controlled and traceable. Our structured approach to change management ensures that changes are handled systematically, supporting consistent quality and patient safety.
Labelling solutions for the pharmaceutical and healthcare sectors
Pharmaceutical and healthcare applications place demanding requirements on labelling, quality and traceability. We offer a broad range of labels and functional labelling solutions for different products, packaging and applications, including:
- Pharmaceutical labels
- Labels for pharmaceutical packaging
- Vial labels
- Syringe labels
- Ampoule labels
- Medical device labels
- Diagnostic and laboratory labels
- Hospital and pharmacy labels
- Cryogenic labels
- Labels for sterile applications
- Medication bags
- Multi-layer labels, including two- and three-layer constructions
- Instructions for use (IFUs), leaflets and package leaflets
- Tamper-evident labels
- Security labels
- Braille labels
- RFID and traceability labels
- Functional labels, including hanger labels
- Ribbons for overprinting
We also help you select the right materials, adhesives and label construction to ensure reliable performance throughout the product lifecycle, from production to end use.
Sequential numbering
Sequential numbering supports traceability, quality control and packaging security. It enables reconciliation checks to confirm that the correct number of pharmaceutical packs has been produced and accounted for. This is particularly important during product recalls, when individual packs may need to be traced.
Braille
For many medicines, Braille is an essential part of the labelling. Adding Braille directly to a label or pack helps people with visual impairments identify their medicines safely. Nordvalls produces labels with high-quality Braille embossing, designed to meet applicable regulatory requirements and provide clear, readable tactile information.
Vision Inspection
Nordvalls offers advanced Vision Inspection for customers who require additional checks on label quality, legibility and accuracy. Vision Inspection is a camera-based system that automatically checks each label against an approved reference. It detects deviations as they occur, helping to reduce the risk of incorrect labels reaching the customer.
Frequently asked questions about pharmaceutical labels
What is GMP?
GMP (Good Manufacturing Practice) is a set of internationally recognised requirements and principles for ensuring that medicines are consistently produced and controlled, with a focus on quality, safety and traceability.
GMP covers documented processes, hygiene, training, risk management, quality control, traceability and change management. Its purpose is to minimise the risk of errors, mix-ups and contamination throughout manufacturing.
At Nordvalls, we apply GMP principles where relevant to the application and the customer’s requirements. With procedures aligned with GMP principles, documented processes and full traceability, we supply pharmaceutical labels for demanding, regulated environments.
What is a tamper-evident label?
A tamper-evident label is a security label that provides visible evidence that a product or pack has been opened or tampered with. Breaking or removing the label leaves visible signs, making unauthorised access easier to detect and supporting patient and product safety.
Tamper-evident labels are widely used in pharmaceuticals, medical devices and healthcare to help protect products throughout the supply chain and show users whether a pack’s seal remains intact.
Nordvalls offers a range of tamper-evident solutions tailored to the product and application. Labels can leave a permanent pattern or message, break apart when removed or be designed so they cannot be resealed without visible evidence of tampering.
By combining security materials with high-quality printing and advanced quality control, we help customers strengthen brand protection and confidence in their products.
What are the requirements for Braille on pharmaceutical packaging?
In the EU, Braille is generally required on the outer packaging of prescription medicines and many non-prescription medicines. It helps people with visual impairments identify their medicines safely and independently.
In most cases, the medicine’s name must appear in Braille. Strength and pharmaceutical form may also be needed to distinguish it from other versions.
Braille embossing needs to meet applicable requirements for dot height, positioning and readability so that it works effectively in practice.
Nordvalls produces Braille labels and other pharmaceutical labels with precision and consistent quality. Our quality control processes help ensure that Braille embossing meets demanding requirements for patient safety and regulatory compliance.
Which label materials are suitable for cryogenic applications and sterilisation?
Cryogenic applications, where products are exposed to very low temperatures, typically require specially developed synthetic materials, such as polypropylene (PP) or polyester (PET), combined with adhesives designed for extreme conditions.
Cryogenic labels are used in pharmaceuticals, laboratories and medical technology to identify vials, test tubes and other containers stored in freezers. Depending on the specification, they can withstand ultra-low temperatures such as −80°C or, in some cases, temperatures as low as −196°C in liquid nitrogen, while maintaining adhesion and legibility. Labels may also need to withstand repeated freezing and thawing.
Sterilisation places different demands on a label. Materials and adhesives need to withstand the specified process, such as steam sterilisation in an autoclave, ethylene oxide (EtO) or gamma irradiation, without lifting, deforming or compromising print quality.
The right material depends on the application, the packaging surface and the conditions the label will encounter. Nordvalls helps you choose the right combination of material and adhesive for clear print, traceability and reliable performance.
Why do pharmaceutical companies choose Nordvalls as their label partner?
We combine specialist expertise, quality and regulatory understanding to deliver label solutions that meet the demanding requirements of the pharmaceutical industry.
- Regulatory expertise – processes aligned with GMP principles, documented traceability and a strong focus on quality and patient safety.
- High quality – labels and materials developed for critical applications.
- Advanced quality control – our dedicated Pharma Line, with Vision Inspection available on request, supports demanding label quality requirements.
- Risk reduction throughout production – structured change management, validated working procedures and documented quality processes support reliable, consistent production.
- A long-term partner – technical advice, material expertise and personal service from development to finished label.
With Nordvalls, you gain a label partner who helps you maintain quality, traceability and patient safety throughout the product lifecycle.