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SFDA and Singapore’s Health Sciences Authority Sign MoU to Strengthen Regulatory Cooperation and Knowledge Exchange

Food
Drugs
Medical Devices
Cosmetics

SFDA and Singapore’s Health Sciences Authority Sign MoU to Strengthen Regulatory Cooperation and Knowledge Exchange

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 The CEO of the Saudi Food and Drug Authority (SFDA), H.E. Dr. Hisham S. Aljadhey, met today with the Chief Executive Officer of Singapore’s Health Sciences Authority (HSA), Adjunct Professor (Dr) Raymond Chua. The meeting took place on the sidelines of Dr. Aljadhey’s visit to Singapore to participate in the 30th Annual Meeting of the International Medical Device Regulators Forum (IMDRF) and the Drug Information Association (DIA) Singapore Annual Meeting.

 The meeting explored strengthening cooperation in the regulation of pharmaceuticals and medical devices, and exchanged expertise and information regarding artificial intelligence applications in regulatory functions. Discussions also centered on opportunities to optimize medical device regulatory systems and establish frameworks for the mutual recognition of Good Manufacturing Practices (GMP).

 Following the bilateral meeting, H.E. Dr. Aljadhey and Adj Prof Chua signed a Memorandum of Understanding (MoU) between the SFDA and the HSA. The MoU aims to foster cooperation and facilitate the exchange of expertise, information, and best practices in product regulation and oversight; thereby enhancing regulatory efficiency and ensuring product safety and quality.

 Under the terms of the MoU, both authorities will exchange technical regulations, legislation, standards, and operational best practices related to areas under their jurisdiction. It also covers pre-market cooperation in product registration; scientific assessments and risk evaluations; laboratory testing and reference analysis; supply chain oversight, inspection mechanisms, product clearance, and traceability; and clinical trials.

 Additionally, the agreement includes post-market information exchanges such as product safety alerts. Both authorities will also collaborate on exchanging information and best practices on regulating novel and innovative products, including advanced applications in biotechnology and artificial intelligence. 

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