CE Marking for Medical Devices in Algeria | EU MDR & IVDR Compliance

 Operon Strategist provides complete CE Marking consulting services for medical device and IVD manufacturers in Algeria. Our team helps you comply with EU MDR 2017/745 and IVDR 2017/746 regulations, covering device classification, technical documentation, and clinical evaluations. We coordinate with Notified Bodies, guide you in appointing an EU Authorized Representative, and support ISO 13485 quality system implementation. With CE Marking, Algerian manufacturers can legally sell devices across the European Economic Area (EEA), gain international recognition, and access EU tenders and reimbursement systems. Partner with Operon Strategist to streamline your CE compliance process and successfully expand into the European market.

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