This episode breaks down the essential documentation required for medical device registration with the UAE's Ministry of Health and Prevention (MOHAP). We explore the complete technical dossier, from the Free Sale Certificate and ISO 13485 to bilingual labeling and clinical data. A key focus is clarifying the "simplified pathway" for devices with prior CE or FDA approval, explaining how it impacts the review process without reducing the amount of paperwork required for a successful submission. Key Questions: • What is the UAE's key regulatory authority for medical devices? • What core documents are required in a MOHAP technical dossier? • Do device labels and instructions need to be in Arabic? • Can a prior CE Mark or FDA clearance get you to the UAE market faster? • What does the "simplified pathway" for MOHAP registration really mean? • Do you still need to submit a full technical file even with prior FDA/CE approval? • Why is robust clinical and risk data non-negotiable for the UAE? Ready to turn these insights into your competitive edge? Pure Global’s regulatory experts guide MedTech companies through every step of 30+ markets worldwide. Explore how we can accelerate your market entry at https://pureglobal.com or email [email protected] for tailored support.