ADIN believes that high quality standards and principles are the essential foundations for ensuring above and beyond customer satisfaction.
Therefore, ADIN implements its quality guidelines in all aspects of daily internal and external business, and the responsibility for maintaining this policy is entrusted onto each and every company employee.
The key to our professional strategic approach is continuously innovating and improving our processes, while aligning our quality policy with our customers’, patients’ and partners’ needs.
In our efforts to ensure constant delivery of high quality products and solutions, ADIN facilities are regularly audited by internal and external authorities.
ADIN’s certification range covers the design, development, manufacturing, marketing, logistics, sales, order processing and distribution of our products, solutions and services.
ADIN’s commitment to quality is reflected in its demanding quality management system, which is compliant with laws and regulations in the Medical Device field, including, but not limited to:
– EU MDD 93/42/ECC as amended by 2007/47EC
– ISO 13485:2016
– US FDA 21CFR 820
– ISO 13485:2016 (MDSAP Audit Model Edition 2) for Australia, Canada & USA