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Quality Assurance Apostille for Mexico
To validate compliance for exporting products or manufacturing services in Mexico, your Quality Assurance certificates require an apostille. Mexico Apostille facilitates this process, ensuring your U.S.-issued quality documents are legally recognized by Mexican officials.
ISO Certifications Examples
| ISO Certification | Category | Common Certification Bodies |
|---|---|---|
| ISO 13485 Medical Devices - Quality Management Systems | Quality & Risk Management | BSI, TÜV SÜD, SGS, DNV, Intertek, Bureau Veritas |
| ISO 9001 Quality Management Systems | Quality & Risk Management | BSI, SGS, TÜV Rheinland, DNV, Bureau Veritas, Lloyd’s Register |
| ISO 14971 Application of Risk Management to Medical Devices | Quality & Risk Management | TÜV SÜD, BSI, Intertek, SGS |
| ISO 31000 Risk Management Principles and Guidelines | Quality & Risk Management | DNV, SGS, Bureau Veritas, TÜV SÜD |
| ISO 22301 Business Continuity Management Systems | Quality & Risk Management | BSI, DNV, SGS, Bureau Veritas |
| ISO 20417 Medical Devices - Information Requirements | Medical Devices | TÜV SÜD, BSI, SGS |
| ISO 15223-1 Medical Devices - Symbols | Medical Devices | BSI, TÜV Rheinland, SGS |
| ISO 11607-1 Packaging for Terminally Sterilized Medical Devices | Medical Devices | TÜV SÜD, BSI, DNV |
| ISO 11607-2 Validation Requirements for Packaging Processes | Medical Devices | TÜV SÜD, BSI, SGS |
| ISO 11135 Sterilization of Health Care Products - Ethylene Oxide | Medical Devices | TÜV SÜD, BSI, SGS |
| ISO 11137-1 Sterilization of Health Care Products - Radiation | Medical Devices | TÜV Rheinland, BSI, DNV |
| ISO 11137-2 Establishing the Sterilization Dose | Medical Devices | BSI, SGS, Intertek |
| ISO 17665-1 Sterilization of Health Care Products - Moist Heat | Medical Devices | BSI, TÜV SÜD, SGS |
| ISO 11737-1 Sterilization of Medical Devices - Microbial Methods | Medical Devices | TÜV SÜD, Intertek, BSI |
| ISO 11737-2 Tests of Sterility | Medical Devices | BSI, SGS, DNV |
| ISO 10993-1 Biological Evaluation of Medical Devices - Risk Management | Medical Devices | BSI, TÜV Rheinland, SGS |
| ISO 10993-5 Tests for In Vitro Cytotoxicity | Medical Devices | TÜV SÜD, SGS |
| ISO 10993-10 Tests for Irritation and Skin Sensitization | Medical Devices | BSI, SGS, DNV |
| ISO 14155 Clinical Investigation of Medical Devices | Medical Devices | BSI, DNV, TÜV SÜD |
| ISO 23908 Sharps Injury Protection - Requirements | Medical Devices | BSI, SGS, Intertek |
| ISO 80369-1 Small-bore Connectors for Medical Liquids and Gases | Medical Devices | BSI, TÜV SÜD |
| ISO 80369-7 Connectors for Intravenous Applications | Medical Devices | BSI, SGS |
| ISO 18562-1 Biocompatibility Evaluation of Breathing Gas Pathways | Medical Devices | TÜV SÜD, BSI |
| ISO 5840-1 Cardiovascular Implants - Cardiac Valve Prostheses | Medical Devices | BSI, TÜV SÜD |
| ISO 25539-1 Cardiovascular Implants - Endovascular Devices | Medical Devices | BSI, DNV |
| ISO 21534 Non-active Surgical Implants - Joint Replacement Implants | Medical Devices | BSI, TÜV Rheinland |
| ISO 7207-1 Implants for Surgery - Femoral Heads | Medical Devices | BSI, SGS |
| ISO 6474-1 Implants for Surgery - Ceramic Materials | Medical Devices | BSI, SGS, Intertek |
| ISO 15378 Primary Packaging Materials for Medicinal Products - GMP | Pharmaceuticals & Biotech | SGS, BSI, TÜV SÜD, DNV |
| ISO 21990 Single-Use Systems for Pharmaceutical Production | Pharmaceuticals & Biotech | BSI, DNV, Intertek |
| ISO 22519 Preparation of Water for Injections | Pharmaceuticals & Biotech | SGS, TÜV SÜD |
| ISO 8362-1 Injection Containers and Accessories | Pharmaceuticals & Biotech | BSI, TÜV Rheinland |
| ISO 8871 Elastomeric Parts for Parenterals and Devices | Pharmaceuticals & Biotech | BSI, SGS |
| ISO 11040-4 Pre-filled Syringes - Glass Barrels | Pharmaceuticals & Biotech | BSI, TÜV SÜD |
| ISO 17225 Cleanrooms and Controlled Environments | Pharmaceuticals & Biotech | BSI, SGS, DNV |
| ISO 14644-1 Classification of Air Cleanliness | Pharmaceuticals & Biotech | BSI, SGS, TÜV SÜD |
| ISO 14644-2 Monitoring for Cleanroom Performance | Pharmaceuticals & Biotech | BSI, DNV, SGS |
| ISO 14698-1 Biocontamination Control - Principles and Methods | Pharmaceuticals & Biotech | BSI, DNV |
| ISO 14698-2 Evaluation and Interpretation of Biocontamination Data | Pharmaceuticals & Biotech | BSI, TÜV SÜD |
| ISO/IEC 17025 Testing and Calibration Laboratories | Laboratory & Info Security | TÜV SÜD, SGS, BSI, DNV |
| ISO 15189 Medical Laboratories - Quality and Competence | Laboratory & Info Security | BSI, DNV, TÜV Rheinland |
| ISO 20387 Biobanking - General Requirements | Laboratory & Info Security | BSI, SGS |
| ISO/IEC 27001 Information Security Management Systems | Laboratory & Info Security | BSI, SGS, TÜV Rheinland, Bureau Veritas |
| ISO 27799 Health Informatics - Information Security | Laboratory & Info Security | BSI, TÜV SÜD |
| ISO 18601 Packaging and the Environment - General Requirements | Supply Chain & Usability | BSI, SGS, TÜV Rheinland |
| ISO 22000 Food Safety Management Systems (for APIs/excipients) | Supply Chain & Usability | SGS, Bureau Veritas, DNV, TÜV SÜD |
| ISO 14001 Environmental Management Systems | Supply Chain & Usability | SGS, Bureau Veritas, DNV, TÜV SÜD |
| ISO 45001 Occupational Health and Safety Management Systems | Supply Chain & Usability | SGS, Bureau Veritas, TÜV Rheinland, DNV |
| ISO 62366-1 Application of Usability Engineering to Medical Devices | Supply Chain & Usability | BSI, TÜV SÜD |
| ISO 23656 Quality Management Systems for Regulatory Auditing Organizations | Supply Chain & Usability | BSI, DNV, TÜV SÜD |