Navigate Medical Device Regulations with Confidence via ISO 13485 Certification in Oman The global medical device regulatory environment is complex and constantly evolving, with stringent requirements from the EU MDR, GCC, and other regions. For businesses in Oman, navigating this landscape while ensuring product safety and market access is a significant challenge. A certified Qualit... https://www.qualitcert.com/iso-13485-certification-consulting-service-in-oman/