Thursday, October 20, 2022

SFDA Medical device Registration & regulations

 

Saudi Arabia is evolving as growing market for healthcare sector, there are huge opportunities which are attracting to medical device manufacturers. Medical device manufacturers need to register their device with SFDA and obtain a certificate from MDMA (Medical Device Market Authorization) as per the MDIR (Medical Device Interim Regulations) Saudi Arabia. MDMA is needed for high-risk devices whereas low risk devices (non- sterile, non-measuring) don’t require prolonged MDMA.

If you are a new manufacturer or already active commercially, we Team of Operon Strategist ensure compliance and efficient regulatory support through 

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1 comment:

  1. Allied Way India - HDPE Blow Moulding Machine Manufacturers in IndiaJanuary 17, 2024 at 3:03 AM

    I read your post, as you share the information about SFDA Medical device. Thank you for sharing. https://www.alliedwayindia.com/disposable-syringe-manufacturing-plant.html

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