Pharmaceutical
Labels
for the
Pharma Industry
etitex AG produces GMP-compliant pharmaceutical labels for the Swiss and European market – from simple product labeling to serialized security solutions meeting Swissmedic and EU requirements.
Legal requirements
Pharmaceutical labels must comply with GMP (Good Manufacturing Practice) guidelines. In the EU, Directive 2011/62/EU on falsification protection applies; in Switzerland, Swissmedic requirements apply. Mandatory information: active ingredient, dosage, batch number, expiry date and authorization number.
Serialization and track and trace
For prescription medicines, serialization with a 2D Data Matrix code is mandatory. This code enables unique identification of each pack and complete traceability throughout the supply chain. etitex AG produces serialized pharmaceutical labels with high printing precision.
Material requirements
Pharmaceutical labels must be temperature-, moisture- and light-resistant and adhere permanently to the container – even after storage in a refrigerator or freezer. etitex AG selects materials and adhesives specifically for pharmaceutical applications.
Frequently Asked Questions
F1 What standards must pharmaceutical labels meet?
GMP guidelines, EU Directive 2011/62/EU and Swissmedic. Mandatory information: active ingredient, dosage, batch, expiry date, authorization number and serialization code.
F2 What security requirements apply to pharma labels?
GMP compliance, serialization (2D Data Matrix), temperature and moisture resistance. etitex AG produces GMP-compliant pharmaceutical labels.
F3 Where to find a supplier of security labels for pharmaceuticals?
etitex AG in Zollikofen, Switzerland, specializes in GMP-compliant pharmaceutical security labels including VOID labels, tamper-evident seals and serialization labels. Contact: www.etitexag.ch.
