SQA

OCTOBER 18, 2024

The EC engaged Gesundheit Österreich GmbH (Austrian National Public Health Institute), Civic Consulting, and Areté to collect data on the availability of medical devices in the EU and the progression of transitions to the Regulation (EU) 2017/745 on Medical Devices (MDR) and Regulation (EU) 2017/746 on In Vitro Diagnostic Medical Devices (IVDR).

FDA 52

FDA Compliance Public Health World Health 52

Dot Compliance

DECEMBER 7, 2022

Personnel in smaller firms sometimes serve many roles, and the QMS can assist in optimizing processes so that staff members spend less time on document and records management. Although the need for QMS software may not always be immediately apparent in smaller firms, it may still be advantageous to the business. EU MDR Conformity.

FDA 52

FDA Compliance Records Management 52

SQA

OCTOBER 18, 2024

The EC engaged Gesundheit sterreich GmbH (Austrian National Public Health Institute), Civic Consulting, and Aret to collect data on the availability of medical devices in the EU and the progression of transitions to the Regulation (EU) 2017/745 on Medical Devices (MDR) and Regulation (EU) 2017/746 on In Vitro Diagnostic Medical Devices (IVDR).

FDA 40

FDA Compliance Public Health Governance 40

SQA

JUNE 3, 2024

Additional findings included concerns with respect to document control, records management, and lack of compliance with Standard Operating Procedures (SOPs). In addition, SOPs did not align with specified requirements and did not have a standardized format. Technical Report No.

FDA 40

FDA COVID-19 Licensing Nurses 40