S.A.L.F has obtained the MDSAP registration certificate

Promoted by the Regulatory Authorities of 5 different countries (Australia, Brazil, Canada, Japan and the United States of America), MDSAP (Medical Device Single Audit Program) is a program that allows accredited organizations (Auditing Organizations – AO) to conduct a single audit of medical device manufacturers to ascertain that they meet the quality system management requirements (GMP: Good Manufacturing Practice) of all reference countries.

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The achievement of the MDSAP registration certificate, attests that Salf designs and produces MDs according to high quality standards in compliance with European, American, Japanese, Canadian and Australian regulations.