We develop drug delivery devices, diagnostic and medical products, as well as primary packaging pursuant to regulations (e.g. MDR 2017/745, ISO 13485, ISO 15378, FDA 21 CFR 820). Our product development process makes it possible for us to react flexibly to the product requirements and to thereby observe the necessary regulatory and normative requirements. Your advantage here is that we have access to many years of experience and closely networked internal capacities. We develop a product for subsequent robust production, whether for a limited number of products for a clinical study, which need to be available quickly, or for high-volume mass production.