Medical Devices Including Medicinal Substance
DEKRA Medical Services
You can call on DEKRA for product certification and certification of your quality management system according to ISO 13485.
When you choose DEKRA, you’re choosing more than just a certifier with an outstanding international reputation. We operate virtually everywhere in the world and our project managers have a background in the medical device or IVD industry, mostly in R&D and/or manufacturing. We participate in all the MRAs and are officially recognized by the FDA and Health Canada.
We’re a reliable, flexible, responsible partner.
- You’re allocated your own Project Manager
- We’re a full service provider (combining CE certification with ISO 13485 audits, thus saving you considerable time and money)
- Modular reviews, pre-approval of clinical protocols and regulatory pathways
- We offer a fixed programme for Transfer of Certification.
We’re experts in complex regulatory and technical projects and proud to be one of the five largest Notified Bodies in the world. The quality, knowledge, and service of DEKRA are a benchmark in the medical industry.