Events / News
Pharmapack 2025 Paris
Please visit us at the next Pharmapack
22 - 23 January 2025 in Paris
Stand Number D102
CPHI 2025 Frankfurt
Please visit us at the next CPHI
28 - 31 October 2025 in Frankfurt
Stand Number B18
Platinum Pharma Supplier Award by Qualifyze
Qualifyze offers a quality assurance program that facilitates supplier audits in the healthcare and pharmaceutical industry. The platform simplifies and centralizes audit management for various locations, providing optimal support for manufacturers, suppliers, and auditors.
As part of this program, our company was reviewed and awarded the Platinum Pharma Supplier Award, recognizing the high quality and reliability of our products and services.
Oni Aquaclean
In order to meet the high demands of our customers and to make a positive ecological contribution, we have decided to treat our cooling water without chemical agents in future.
With the new system, the water is treated accordingly using mechanical filters and UV light.
Capacity expansion for PP28 closures
Due to constantly increasing demand for our child-resistant closure solutions, we are expanding our production capacities in this field.
The new moulds and machines will further increase the process reliability and the high quality of our closures.
New version of PP28 closure “Vienna”
With our PP28 closure "Vienna" with sealing cone we are welcoming a new member to our "Vienna" design family: 11.191.00 Dk3
- economical solution, thanks to simple one-piece production (interesting for projects with restrained budget)
- seals tightly by means of a sealing cone and is suitable for PP28 bottlenecks with an inner diameter of 20mm
- ideal functionality due to integrated tamper-evidence ring
Implementation of a new injection moulding machine
We are modernising the machinery in our certified clean room.
This will enable us to guarantee the production-quality of our high-grade primary packaging and medical devices.
Medical Devices and MDR
Since 2009 we are certified according to ISO 15378, GMP for pharmaceutical primary packaging an even longer according to ISO 13458 and Directive 92/43 for medical devices and the CE-marking.
This is now being replaced by the new MDR (Medical Device Regulation) and with the expiry of the transitional period, new medical devices in the EU can now only be developed and placed on the market under the valid MDR.
As we have already completed certification in 2023, we can continue to develop and produce new medical devices in the EU together with our partners!
We look forward to your inquiries!
