A three-day training course on medical equipment standards was conducted at the Food and Drug Administration of Iran University of Medical Sciences (IUMS). This event brought together experts from various institutions, including Iran University of Medical Sciences, Tehran University of Medical Sciences, and Shahid Beheshti University of Medical Sciences.

According to the public relations report from the Food and Drug Administration, the course was facilitated in collaboration with distinguished professors experienced in auditing and standards for medical equipment.

Participants engaged in comprehensive training covering specialized topics such as the ISO 13485 standard, Medical Device Regulation (MDR) requirements, and the Post-Market Clinical Follow-up (PMCF) process. The curriculum was designed to provide both theoretical knowledge and practical applications.

The primary objective of this course was to enhance the knowledge and skills of professionals in the medical equipment sector, equipping them with a thorough understanding of international standards and regulatory processes within the healthcare system.