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Results for tag: "Device Master Record"

The FDA QMSR and the Key Elements of QSIT cGMP Inspection and Audits for Medical Device Manufacturers (Recorded) - Product Thumbnail Image

The FDA QMSR and the Key Elements of QSIT cGMP Inspection and Audits for Medical Device Manufacturers (Recorded)

  • Training
  • September 2025
  • 2 Days
  • Global
From
Bottlenecks to Flow: Optimizing Design Controls and Validation in Medical Device QMS (Recorded) - Product Thumbnail Image

Bottlenecks to Flow: Optimizing Design Controls and Validation in Medical Device QMS (Recorded)

  • Training
  • October 2025
  • 2 Days
  • Global
From
US FDA Medical Device Quality System (QSR) Compliance: Design Controls, Verification & Validation (Recorded) - Product Thumbnail Image

US FDA Medical Device Quality System (QSR) Compliance: Design Controls, Verification & Validation (Recorded)

  • Training
  • October 2025
  • 2 Days
  • United States
From
Transcatheter Mitral Valve Repair (TMVR) Devices (Cardiovascular Devices) - Medical Devices Pipeline Product Landscape, 2021 - Product Thumbnail Image

Transcatheter Mitral Valve Repair (TMVR) Devices (Cardiovascular Devices) - Medical Devices Pipeline Product Landscape, 2021

  • Report
  • October 2021
  • 77 Pages
  • Global
From
Design History File (DHF), Device Master Record (DMR), and Device History Record (DHR) for Medical Devices (Recorded) - Product Thumbnail Image

Design History File (DHF), Device Master Record (DMR), and Device History Record (DHR) for Medical Devices (Recorded)

  • Training
  • May 2025
  • 4 Hours
  • Global
From
3-Hour Virtual Seminar on US FDA and EU Medical Device Directive Requirements for DHF, DMR, DHR and TF/DDS (Recorded) - Product Thumbnail Image

3-Hour Virtual Seminar on US FDA and EU Medical Device Directive Requirements for DHF, DMR, DHR and TF/DDS (Recorded)

  • Training
  • March 2024
  • 3 Hours
  • Europe, United States Europe, United States
From
Design History File (DHF), Device Master Record (DMR), and Device History Record (DHR) for Medical Devices Training (November 13, 2025) - Product Thumbnail Image

Design History File (DHF), Device Master Record (DMR), and Device History Record (DHR) for Medical Devices Training (November 13, 2025)

  • Training
  • November 2025
  • 4 Hours
  • Global
From
Mastering DHF, DMR, and DHR: Essential Documentation in Medical Device Manufacturing Webcast - Webinar (Recorded) - Product Thumbnail Image

Mastering DHF, DMR, and DHR: Essential Documentation in Medical Device Manufacturing Webcast - Webinar (Recorded)

  • Webinar
  • November 2024
  • 4 Hours
  • Global
From
Design History File (DHF) Remediation using Principles of Lean Documents and Lean Configuration - Product Thumbnail Image

Design History File (DHF) Remediation using Principles of Lean Documents and Lean Configuration

  • Training
  • 90 Minutes
  • Global
DMR & DHR - What Is Really Required - Product Thumbnail Image

DMR & DHR - What Is Really Required

  • Training
  • 90 Minutes
  • Global
cGMPs for Medical Devices, Including In Vitro Diagnostic Devices - Product Thumbnail Image

cGMPs for Medical Devices, Including In Vitro Diagnostic Devices

  • Training
  • 90 Minutes
  • Global
The FDA's Outlook for Quality in Device Manufacturing - Product Thumbnail Image

The FDA's Outlook for Quality in Device Manufacturing

  • Training
  • Global
Preparing for FDA's Unique Device Identification Rule - Product Thumbnail Image

Preparing for FDA's Unique Device Identification Rule

  • Training
  • 90 Minutes
  • Global
Understanding FDA Design Verification and Validation Requirements for Medical Devices - Product Thumbnail Image

Understanding FDA Design Verification and Validation Requirements for Medical Devices

  • Training
  • 75 Minutes
  • Global
Medical Device Development: Regulation and Law, All New Edition! - Product Thumbnail Image

Medical Device Development: Regulation and Law, All New Edition!

  • Book
  • September 2009
  • 600 Pages
Design History Files (DHF), Device Master Records (DMR), Device History Records (DHR), Technical Documentation Files - The US FDA and EU MDR Requirements - Webinar (Recorded) - Product Thumbnail Image

Design History Files (DHF), Device Master Records (DMR), Device History Records (DHR), Technical Documentation Files - The US FDA and EU MDR Requirements - Webinar (Recorded)

  • Webinar
  • January 2022
  • 90 Minutes
  • United States, Europe United States, Europe
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  • 16 Results (Page 1 of 1)
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The Device Master Record (DMR) market is a subset of the medical device industry. It is a system of records that document the design, development, production, and distribution of medical devices. The DMR is used to ensure that medical devices meet regulatory requirements and are safe and effective for their intended use. It is also used to track changes to the device over time. The DMR market is highly regulated and requires companies to adhere to strict standards. Companies must have a comprehensive system in place to ensure that all records are accurate and up-to-date. Companies must also have a system in place to track changes to the device over time. The DMR market is an important part of the medical device industry. It helps ensure that medical devices are safe and effective for their intended use. Companies in the DMR market include Siemens Healthineers, Medtronic, Johnson & Johnson, Philips, and Abbott. Show Less Read more