01
Primary container labels
For vials, ampoules, syringes, bottles and cans. Small radii, condensation and refrigeration limit the construction. We qualify material, adhesive and print on the actual container, not on the data sheet.
Industry solution
Labels for Pharmaceuticals Marking that follows the batch all the way to dispensing
From the vial through the carton to the investigational product: in pharma every label carries a batch identity that has to stay traceable for years. We manufacture to your specification and transfer your approved data faithfully into print.
Labels and printed documents
What gets marked in the pharmaceutical industry
From the primary container to the pallet, and the right document for every batch.
02
Cartons with safety features
For prescription medicines within the scope of the falsified medicines rules. We print the unique identifier as a 2D code and in plain text from your data; allocation and verification stay with you.
03
Tamper evident and closure labels
For carton flaps and other opening points. Whether tampering becomes visible depends on the combination of label, adhesive and board. That is why we sample on the original packaging rather than promise it.
04
Cold chain and deep freeze labels
For refrigerated medicines, samples and shipping containers. Material codes exist rated from −25 °C application to −60 °C service. Whether they suit your chain depends on the substrate and the moment of application.
05
Clinical trial labels
For investigational products, kits and outer packaging. Small formats, many languages, re-labelling and blinding. Content, randomisation and release come from the sponsor, we reproduce them faithfully.
06
Batch and accompanying records
Batch records, label reconciliation records, certificates of analysis, temperature logs and package leaflets. As numbered single sheets, continuous sets or carbonless sets to your template.
Matching products
Products for the pharmaceutical industry
What we produce for this industry, sorted by product area. Each card leads to the product page with materials and versions.
Technical basis
What we discuss before choosing the material
A material recommendation without container, medium, temperature profile and storage time is guesswork. We clarify these four points with you.
- Substrate
- Vials and ampoules: small radii and little bonding area limit format and construction
- Carton board reacts differently to adhesives depending on varnish and surface
- Condensation on refrigerated containers decides whether application works at all
- Chemical resistance
- Disinfectants and isopropanol: agent, contact time and repetition determine the result
- None of our materials is tested for direct contact with the medicine, that belongs to primary packaging
- Water and condensation are manageable, oil and grease considerably less so
- Temperature
- Application and service temperature are two different values, and both belong in the specification
- For the cold chain there are material codes rated from −25 °C application to −60 °C service
- Dry ice, autoclave and gamma have to be qualified separately per method and cycle
- Code quality
- The 2D code on the carton decides whether verification succeeds at the point of dispensing
- Small modules on curved containers are the main risk for weak grades
- We grade printed codes to ISO/IEC 15415 and hand over the measurement report
Mandatory information
How your data reaches the label
Pharmaceutical responsibility stays with the marketing authorisation holder. What we take on is the faithful transfer of your approved data into print and code.
- Batch, expiry and serial data taken faithfully from your approved source
- Country and language variants from one maintained set rather than from single orders
- Repeat orders with a documented material code and a recorded layout version
More room on a small container.. Pull the corner, like a multi-layer label on a vial.. Mandatory texts in many languages. The bonding area stays small. Open and close again
hummel360°
When the problem is not the label but the process before it
Batch, expiry and market data already sit in your ERP or document system. With hummel360° we map how they turn into ordering, print data and traceable processes. Built around your batch run, not off the shelf.
Call up approved variants under control
Products, markets and language versions sit in a protected ordering workflow, and every site sees only what is approved for it. You decide who may do what.
Variable data without retyping
Batch, expiry and ID data arrive as a file or through an interface and become print data by rule. Mapping your fields is set up in the project.
Stock per site in view
Reorder levels, alerts and a complete movement journal show what is where and when to reorder. Postings are made by scanning a barcode with a phone.
Quality you can verify
Our certifications & partnerships
- EcoVadisSilver rating · Top 15% (September 2026)
- ClimatePartnerClimate contribution available per order
- ISO 9001Quality management
- ISO 14001:2015Environmental management (QAS International) · Certificate no. GMEN1114
- VskE memberlabels association
- FSC® C006747Responsible forestry
- EN 16247-1Energy audit
Let us talk about your marking
Send us the container, medium, temperature profile and storage time, and we will sample the matching construction.
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Your contact team
Let's solve your labeling challenges together.
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