Regulatory Compliance

Overview of Medical Device Regulation in Oman The healthcare sector in Oman is expanding rapidly, offering major opportunities for medical device manufacturers worldwide. However, before entering this growing market, understanding the medical device regulation in Oman is crucial. The Directorate General of Pharmaceutical Affairs and Drug Control (DGPADC) under the Ministry of Health (MoH) oversees […]

Why Medical Device Labeling Matters in Oman and Globally Medical device labeling plays a crucial role in ensuring product safety, regulatory compliance, and effective usage. For manufacturers in Oman aiming to enter global markets or supply healthcare facilities locally, accurate and compliant labeling is mandatory. Regulatory bodies such as the US FDA, the European Union’s

Introduction: Why Medical Device Registration in Oman Matters Oman’s growing healthcare sector presents a high-potential market for global medical device manufacturers. To legally sell your products in the Sultanate, medical device registration in Oman is mandatory. Regulated by the Directorate General for Pharmaceutical Affairs and Drug Control (DGPA&DC) under the Ministry of Health (MoH), the