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Medical Devices

Desiree Tarranco

April 11, 2025

CAPA Management in the Medical Device Industry: Examples, Requirements, and Process

CAPAMedical Devices

Desiree Tarranco

February 28, 2025

Medical Device Post-Market Surveillance (PMS)

Medical DevicesPost-Market Surveillance

Desiree Tarranco

February 13, 2025

DHF vs. DMR vs. DHR: Differences and Relations

Medical Devices

Desiree Tarranco

February 13, 2025

Device History Record (DHR): Definition, Requirements, and What It Includes

Medical Devices

Desiree Tarranco

February 13, 2025

Device Master Record (DMR): Definition, Requirements, and What It Includes

Medical Devices

Desiree Tarranco

February 3, 2025

Design History File (DHF): Definition and Requirements

Medical Devices

Desiree Tarranco

February 3, 2025

Design Controls: Definition, Requirements, Process, and Phases

Medical Devices

Desiree Tarranco

January 31, 2025

Medical Device Document Control: Definition, Process, and Requirements

Document ControlMedical Devices

Bruna De Lucca Caetano

July 18, 2024

Medical Device Quality Assurance (QA)

Medical DevicesQuality Assurance

Bruna De Lucca Caetano

July 16, 2024

20 Best Medical Device Blogs and Industry News Websites

Medical Devices

Bruna De Lucca Caetano

March 5, 2024

Top 12 Medical Device Startups to Look Out For in 2024

Medical Devices

Bruna De Lucca Caetano

January 22, 2024

EU MDR Medical Device Classification: Classes, Examples

Medical Devices

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