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Search in Medical Devices returned 31,629 results.

US FDA Medical Device QSR (21 CFR 820) / Quality Management System - current and proposed major changes - Product Thumbnail Image

US FDA Medical Device QSR (21 CFR 820) / Quality Management System - current and proposed major changes

  • Training
  • 90 Minutes
  • United States
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
Risk Management for Medical Devices per ISO 14971 2019 - Product Thumbnail Image

Risk Management for Medical Devices per ISO 14971 2019

  • Training
  • 60 Minutes
  • Global
US FDA's AI Framework for Medical Devices - Product Thumbnail Image

US FDA's AI Framework for Medical Devices

  • Training
  • 90 Minutes
  • United States
Usability Principles for Medical Devices: Interpreting and Implementing IEC 62366 - Product Thumbnail Image

Usability Principles for Medical Devices: Interpreting and Implementing IEC 62366

  • Training
  • 90 Minutes
  • Global
eLabeling for Medical Devices: Valuable but not easy - Product Thumbnail Image

eLabeling for Medical Devices: Valuable but not easy

  • Training
  • 90 Minutes
  • Global
Integrating ISO 14971 Risk Analysis into the Product Development Process - Product Thumbnail Image

Integrating ISO 14971 Risk Analysis into the Product Development Process

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

DMR & DHR - What Is Really Required

  • Training
  • 90 Minutes
  • Global
Comparing the Pharmaceutical and Medical Device Product Lifecycles - Product Thumbnail Image

Comparing the Pharmaceutical and Medical Device Product Lifecycles

  • Training
  • 120 Minutes
  • Global
Medical Device Complaints, MDR's and Recalls - Product Thumbnail Image

Medical Device Complaints, MDR's and Recalls

  • Training
  • 60 Minutes
  • Global
Medical Device Software Verification and Validation - Product Thumbnail Image

Medical Device Software Verification and Validation

  • Training
  • 60 Minutes
  • Global
How to Conduct a Human Factors Validation Following ISO 62366 and the 2016 FDA Guidance - Product Thumbnail Image

How to Conduct a Human Factors Validation Following ISO 62366 and the 2016 FDA Guidance

  • Training
  • 60 Minutes
  • Global
Medical Device CE Mark & Quality System Certification: Recent & Proposed Changes - Product Thumbnail Image

Medical Device CE Mark & Quality System Certification: Recent & Proposed Changes

  • Training
  • 60 Minutes
  • Global
FDA Import Alert - 2017 - Product Thumbnail Image

FDA Import Alert - 2017

  • Training
  • 60 Minutes
  • Global
Best Practices for Medical Device Reporting (MDR), Recall, Reports of Corrections and Removals - Product Thumbnail Image

Best Practices for Medical Device Reporting (MDR), Recall, Reports of Corrections and Removals

  • Training
  • 120 Minutes
  • Global
Be Ready for eMDR Going Live August 14, 2015 - Product Thumbnail Image

Be Ready for eMDR Going Live August 14, 2015

  • Training
  • 110 Minutes
  • Global
Basics of Writing Validation Protocols for Medical Devices - Product Thumbnail Image

Basics of Writing Validation Protocols for Medical Devices

  • Training
  • 60 Minutes
  • Global
Documenting & Conducting CAPA Investigations - Product Thumbnail Image

Documenting & Conducting CAPA Investigations

  • Training
  • 60 Minutes
  • Global
Applying Human Factors Best Practices for Medical Device Risk Management - Product Thumbnail Image

Applying Human Factors Best Practices for Medical Device Risk Management

  • Training
  • 60 Minutes
  • Global
Quality Risk Management Using Failure Modes, Effects and Criticality Analysis - Product Thumbnail Image

Quality Risk Management Using Failure Modes, Effects and Criticality Analysis

  • Training
  • 60 Minutes
  • Global
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