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  1. Medical Device Single Audit Program (MDSAP)

ANVISA Resolutions: Medical Device Single Audit Program (MDSAP)

RE nº 2.038/2019

 

Auditing Organization Resolution
BSI Group America Inc. RE nº 651/2017
DEKRA Certification B.V. RE nº 1.054/2019
DQS Medizinprodukte GmbH RE nº 1.055/2019
Intertek Testing Services NA Inc. RE nº 323/2017
GMED RE n°3.568/2109
Lloyd's Register Quality Assurance Inc. RE nº 2.038/2019
National Standards Authority of Ireland (NSAI) RE nº 1.754/2019
NCC Certificações do Brasil Ltda. RE n° 2.710/2020
QMI-SAI Canada Limited RE n° 3.483/2020
SGS United Kingdom Ltd. RE nº 3.432/2017
TUV Rheinland of North America, Inc. RE nº 1.713/2018
TUV SUD America Inc. RE nº 324/2017
TUV USA, Inc. RE n° 2.654/2018
UL Medical and Regulatory Services of UL LLC RE nº 2.226/2017

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