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 |