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Apoio à certificação de dispositivos médicos, dispositivos de diagnóstico in vitro e SaaS / QMS/Regulamentação

NTT DATA Portugal

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NTT DATA Portugal

Support in Post-Market Surveillance (PMS)

Descrição

Support in Post-Market Surveillance (PMS)

Key-words
Post-Market Surveillance
Service Information
MDR/IVD Segment
on demand (consulting) Delivery Format
patricia.mendescalado@nttdata.com Contact

Internal Audit (ISO 13485:2016, RDM) - specializing in Medical Device Software

Descrição

Internal Audit (ISO 13485:2016, RDM) - specializing in Medical Device Software

Key-words
audit ISO 13485:2016
Service Information
MDR/IVD Segment
on demand (consulting) Delivery Format
patricia.mendescalado@nttdata.com Contact

How to maintain the QMS after certification

Descrição

How to maintain the QMS after certification

Key-words
QMS post-certification
Service Information
MDR/IVD Segment
on demand (consulting) Delivery Format
patricia.mendescalado@nttdata.com Contact

Medical device risk management (ISO 14971:2019)

Descrição

Medical device risk management (ISO 14971:2019)

Key-words
risk management
Service Information
MDR/IVD Segment
on demand (consulting) Delivery Format
patricia.mendescalado@nttdata.com Contact

Support for MDR submissions: Technical documentation and QMS ready for audit.

Descrição

Support for MDR submissions: Technical documentation and QMS ready for audit.

Key-words
submission documentation QMS
Service Information
MDR/IVD Segment
on demand (consulting) Delivery Format
patricia.mendescalado@nttdata.com Contact

Support/implementation of Quality Management System (ISO 13485:2016) - specialized in Medical Device Software

Descrição

Support/implementation of Quality Management System (ISO 13485:2016) - specialized in Medical Device Software

Key-words
Quality Management System (QMS)
Service Information
MDR/IVD Segment
on demand (consulting) Delivery Format
patricia.mendescalado@nttdata.com Contact