SFDA Second Annual Conference - Saudi Vision 2030

Saudi Arabia is famous as one of the largest market for the medical device. Due to the hydrocarbon-based economy and As part of the Gulf Cooperation Council (GCC, also known as the economic union of the six Arab states) Saudi Arabia has experienced an extraordinary growth.

For regularization of drugs and medical devices in Saudi Arabia, they have the government agency called the Saudi Food & Drug Authority (SFDA). The legislative, executive, and surveillance are the three responsibilities of Medical Device Sector. Read More about Medical Device Registration in Saudi Arabia

In the field of medical devices operation, SFDA has issued a number of guidelines to assist an organization to understand its obligations under the Interim Regulation and the Implementing Rules.

By enhancing efficiency and transparency, the Saudi Food and Drug Authority seeks to achieve the kingdom of Saudi 2030 vision. Also, set up the necessary environment Kingdom of Saudi Arabia for the Saudi Community and business sector to endure their responsibilities. In addition, take the lead in facing challenges and grab opportunities, which will ensure the food safety, safety, quality and effectiveness of the drug, and the safety and efficiency of medical devices and products. This all was discussed in the recent conference named "Saudi Food and Drug Authority Second Annual Conference" which was held on 25th – 27th September 2018, Saudi Arabia

Objectives Of Saudi Vision 2030 SFDA Second Annual Conference: # Serves as an annual gathering connects SFDA with other stakeholders from the private and public sectors.

• Exchange professional and scientific experiences with SFDA partners from the public and private sector.
• Share up-to-date best practices in regulatory sciences and other relevant disciplines.
• Transfer experiences and enhance knowledge concerning drug, food, medical devices awareness, and health promotion.
• Conduct applied workshops addressing professional and scientific aspects.
• Arranging for an annual exhibition in collaboration with SFDA partners to demonstrate the updated regulatory sciences and related tools.

Medical Devices Topics Were Discussed On:

• Clinical evaluations & investigations for medical devices.
• Medical device regulation.
• Medical devices post market surveillance and vigilance.
• Medical devices testing and calibration.
• Impact of medical device regulation.
• Cyber Security for medical devices.