Label design & production with regulatory support
Labeling solutions tailored to our clients’ specific requirements
Labeling of IMPs and AMPs needs to be carried out in accordance with the well-defined requirements of Regulation (EU) No 536/2014 and GMP Annex 13
Each clinical trial has its own labeling needs, which is why we provide customized services:
Our extensive range of labeling options allows us to tailor solutions to each client’s specific needs:
- Booklet labels, multi-layer and single-layer labels, wrap-around labels, ECL-labels, documentation labels, tamper label, tear-off section, etc. label options
- Variable data, code and identity
- Re-labelling
- JIT labelling
- Senior-Friendly ,child-resistant (SF/CR) package options
- Labelling operations on 2-8°C and 15-25°C, under 100% quality control
Short lead-time label design and production, planned and executed in compliance with applicable regulations, and verified through regulatory oversight.