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Search in Medical Devices returned 31,845 results.

Controlled Document System for a Life Sciences Manufacturing Plant - Principles of Lean Documents and Lean Configuration - Product Thumbnail Image

Controlled Document System for a Life Sciences Manufacturing Plant - Principles of Lean Documents and Lean Configuration

  • Training
  • 90 Minutes
  • Global
Medical Device Complaints Handling Strategies for Managing Your Biggest Compliance Challenge - Product Thumbnail Image

Medical Device Complaints Handling Strategies for Managing Your Biggest Compliance Challenge

  • Training
  • 60 Minutes
  • Global
Post-market Surveillance - Clinical Evaluation and Risk Management - Product Thumbnail Image

Post-market Surveillance - Clinical Evaluation and Risk Management

  • Training
  • 90 Minutes
  • Global
The New US FDA 21 CFR 820, Quality Management System Regulation (QMSR), Medical Device CGMPs - Product Thumbnail Image

The New US FDA 21 CFR 820, Quality Management System Regulation (QMSR), Medical Device CGMPs

  • Training
  • 90 Minutes
  • United States
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
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
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 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
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
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
Effective CAPA Management: How to Implement a Risk-based Approach to Improve Your Quality System - Product Thumbnail Image

Effective CAPA Management: How to Implement a Risk-based Approach to Improve Your Quality System

  • Training
  • 60 Minutes
  • Global
Designing an Effective Cleaning and Disinfection Program for Pharmaceutical, Biotech, and Medical Device Cleanrooms - Product Thumbnail Image

Designing an Effective Cleaning and Disinfection Program for Pharmaceutical, Biotech, and Medical Device Cleanrooms

  • Training
  • 90 Minutes
  • Global
Premarket Approval (PMA) agreement with FDA for the medical device companies - the Requirements - Product Thumbnail Image

Premarket Approval (PMA) agreement with FDA for the medical device companies - the Requirements

  • Training
  • 60 Minutes
  • Global
The Essentials of Food and Drug Administration Medical Device Regulations:A Primer for Manufacturers and Suppliers - Registration, Medical Device Reporting, Corrections and Removals (Recalls) - Product Thumbnail Image

The Essentials of Food and Drug Administration Medical Device Regulations:A Primer for Manufacturers and Suppliers - Registration, Medical Device Reporting, Corrections and Removals (Recalls)

  • Training
  • 90 Minutes
  • Global
The Essentials of Food and Drug Administration Medical Device Regulations: A Primer for Manufacturers and Suppliers - Quality System Regulation - Product Thumbnail Image

The Essentials of Food and Drug Administration Medical Device Regulations: A Primer for Manufacturers and Suppliers - Quality System Regulation

  • Training
  • 90 Minutes
  • Global
Addressing the Elusive Use Error: Meeting Regulatory Expectations for Identifying and Controlling Medical Device Use-Related Hazards - Product Thumbnail Image

Addressing the Elusive Use Error: Meeting Regulatory Expectations for Identifying and Controlling Medical Device Use-Related Hazards

  • Training
  • Global
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