As part of its ongoing efforts to enhance health standards and develop the medical care system, the Sultanate of Oman has obtained associate membership in the International Medical Device Regulators Forum (IMDRF). This follows Oman’s participation in the Forum's recent conference, held in Seattle, USA, where representatives from various countries, medical device regulatory bodies, and experts in regulatory affairs gathered to discuss the latest developments and challenges related to the regulation and use of medical devices.
The Ministry of Health, represented by the Drug Safety Center, participated in the IMDRF. The Center presented remarkable progress achieved in regulating and approving medical devices, highlighted ongoing efforts to develop healthcare infrastructure, and outlined Oman’s regulatory policies and procedures that ensure the quality, safety, and proper circulation of medical devices.
The IMDRF included several panel discussions and workshops focusing on several topics such as harmonizing global standards for medical devices, risk assessment, and recent innovations in medical device technology. The Drug Safety Center shared insights on successful experiences in medical legislation and outlined mechanisms adopted by Oman to improve the management and use of these devices, ensuring patient safety and the effectiveness of healthcare services.
The Forum represents a valuable opportunity for the Sultanate of Oman to strengthen international cooperation in the health sector and exchange expertise with other countries, contributing to an elevated standard of healthcare services. The Drug Safety Center aims to leverage international expertise to foster innovation in medical device regulation and apply best global practices.
The Forum concluded with recommendations to unify international efforts to improve medical device regulation, with participating countries agreeing to continue collaboration to enhance the quality and safety of healthcare worldwide.
