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Great insights into the Saudi Arabian classification system and key regulatory considerations when registering medical devices in Saudi Arabia.
Our Regulatory Intelligence Associate, Baraa Nofal has covered the following topics:
👉 What are the rules that classify the risk of medical devices?
👉What risks are associated with medical device production if they do not comply with SFDA requirements?
👉 What process do producers need to go through the medical devices registration?
👉 What happens once you need to update your approved license?