Hello Everyone,
Previously SFDA was providing two paths for Class I (Non-sterile, Non-measuring) products. They were MDMA (AR required) and MDNR (ARE not required therefore through distributor). Please see attached process chart.
Is it still same or it has been changed with the new portal (GHAD)?
Thanks in advance and best regards.
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Ilker Yilmaz
Int. Regulatory Affairs Manager
Watford
United Kingdom
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