A workshop organized by the Riyadh Chamber, represented by the Health Sector Committee and in cooperation with the Saudi Food and Drug Authority, discussed the role played by the Authority in supporting local manufacturers of medical devices and supplies. The workshop focused on enhancing manufacturers’ awareness of the regulatory framework governing the industry, while reviewing the legislative and regulatory roles that contribute to stimulating local manufacturing and strengthening compliance with approved standards, thereby improving product quality and enhancing competitiveness.

The workshop, attended by a number of specialists and representatives of national factories, addressed the importance of compliance with international standards within the manufacturing ecosystem. It also discussed the requirements for implementing a medical devices quality management system, while highlighting safety and performance requirements as essential pillars for the approval of medical products.​