At SteriInk, product development begins with understanding the customer’s technical needs. The sterilization process, packaging material, printing method, target colour change and production conditions are assessed together to develop a suitable solution.
With over 20 years of R&D experience, we consider performance, manufacturability and application compatibility together in indicator inks, medical packaging films and printed medical solutions.
We carry out technical work at different stages of product development, from laboratory studies and sample production to application testing and production optimisation.
1. Requirements & Technical Analysis
We define the sterilization process, substrate, printing method and target product properties.
2. Formulation & Material Selection
We work on an ink formulation or medical packaging material suited to the application.
3. Sample & Application Tests
The solution is evaluated for printing, substrate compatibility, colour change and application performance.
4. Optimisation
Formulation and process improvements are made based on test results.
5. Production Transfer
A solution that meets the technical requirements is adapted to the production process and prepared for series production.
Yes. Custom product development can be carried out by evaluating the intended use, sterilization process, packaging material, printing method and other technical requirements.
First, the target sterilization process and application conditions are assessed. The solution is then optimised through formulation work, sample preparation, colour change testing, printing tests and application tests.
The compatibility of an existing formulation or product structure can be assessed against the application’s technical requirements, followed by development and optimisation as needed.
Yes. Film structures, medical kraft, printed packaging and other suitable materials can be assessed according to their intended use and production requirements.

