MDSAP
Medical Device Single Audit Program
International Recognition
MDSAP allows for a single regulatory audit of a medical device manufacturer's quality management system that satisfies the requirements of multiple regulatory jurisdictions.
Recognized in 5 major markets: USA, Canada, Japan, Australia, and Brazil
Streamlined regulatory approval process
MDSAP Certificate
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Global Standards
By achieving MDSAP certification, ErythrosLight demonstrates its commitment to meeting the highest international regulatory standards for medical device quality and safety across multiple key markets worldwide.