MDSAP Is A Snap If Your Firm Follows Quality Systems Standard ISO 13485, Auditor Says

NSF International's Brian Ludovico explains why device-makers that already follow international quality systems standard ISO 13485 shouldn't be nervous about taking part in the Medical Device Single Audit Program. Ludovico also shares MDSAP participation numbers and says firms should feel at ease knowing that the program's auditing organizations undergo a rigorous process to become recognized by the MDSAP Regulatory Authority Council.

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Brian Ludovico wants device-makers to know that if they already follow international quality systems standard ISO 13485, then undergoing an MDSAP audit is a snap.

That's because the Medical Device Single Audit Program – which allows firms to undergo one audit by an accredited third party to satisfy quality regulations for the US,

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