The validated final cleaning process at CPM Precision is fully automated and carried out in accordance with the strictest standards on our innovative cleaning system, the effectiveness of which is confirmed by regular tests at certified testing laboratories.
The assembly, packaging, and primary packaging of your medical devices take place in our clean room, which is certified according to ISO class 7. This specially regulated environment complies with the strict specifications of DIN EN ISO 14644-1 regarding the maximum permissible number of particles. Consistent and thorough monitoring guarantees compliance with these standards in order to ensure the highest quality standard for your products.
At your request, we can supplement the primary packaging of your products with a customized folding carton, including labeling. This is accompanied by instructions for use. In order to ensure consistently high quality, the specific labels are not only applied by machine but also automatically verified using advanced camera and weighing technologies.
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We work with you to design a customized packaging solution that includes both primary and final packaging and which is precisely tailored to your requirements and preferences. Even the most complex packaging requirements is within the realm of possibility. We provide you with advice and assistance in selecting the optimum packaging and validating it.
In order to complete the finishing process of your products and to sterilize them if required, we cooperate with experienced external partners in sterilization. We are ready to work with you and our specialists to develop a tailored sterilization validation.
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Our teams of experts provide you with comprehensive advice and work with you to develop the ideal, customized solution for your specific needs. Don’t hesitate – get in touch with us today and take the first step towards your solution.
