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Search in Medical Devices returned 31,629 results.

CAPA Management and Compliance with Regulatory Requirements - Product Thumbnail Image

CAPA Management and Compliance with Regulatory Requirements

  • Training
  • 75 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
IDE (Investigational Device Exemption) for PMA and 510(k) for CDRH and CBER - Product Thumbnail Image

IDE (Investigational Device Exemption) for PMA and 510(k) for CDRH and CBER

  • Training
  • 60 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
Tracking Use Error Risks in Post-Market Surveillance and CAPA Activities - Product Thumbnail Image

Tracking Use Error Risks in Post-Market Surveillance and CAPA Activities

  • Training
  • 60 Minutes
  • Global
Managing the IDE (Investigational Device Exemption) Submission for Compliance Success - Product Thumbnail Image

Managing the IDE (Investigational Device Exemption) Submission for Compliance Success

  • 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
Medical Device Software Risk Analysis - Product Thumbnail Image

Medical Device Software Risk Analysis

  • Training
  • 60 Minutes
  • Global
The CAPA Trap or Common Problems and Pitfalls - Product Thumbnail Image

The CAPA Trap or Common Problems and Pitfalls

  • Training
  • 60 Minutes
  • Global
Ethylene Oxide Sterilizer Validation: Basic Requirements - Product Thumbnail Image

Ethylene Oxide Sterilizer Validation: Basic Requirements

  • Training
  • 60 Minutes
  • Global
Beyond Usable to Valuable: Usability Testing on Medical Device Labeling - Product Thumbnail Image

Beyond Usable to Valuable: Usability Testing on Medical Device Labeling

  • Training
  • Global
4-Region internal audits: Medical Device Quality System audits that cover internal regulatory compliance for FDA, Europe, Canada and Japan - Product Thumbnail Image

4-Region internal audits: Medical Device Quality System audits that cover internal regulatory compliance for FDA, Europe, Canada and Japan

  • Training
  • 60 Minutes
  • Canada, Japan, Europe Canada, Japan, Europe
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
Maintaining an Effective CAPA Program and Using Risk Assessment Tools: Current Trends - Product Thumbnail Image

Maintaining an Effective CAPA Program and Using Risk Assessment Tools: Current Trends

  • Training
  • 60 Minutes
  • Global
ISO 14971:2007 -- The Newly Revised Risk Management Standard for Medical Products - Product Thumbnail Image

ISO 14971:2007 -- The Newly Revised Risk Management Standard for Medical Products

  • Training
  • 60 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
ISO 14971: Understanding and Applying Risk Management - Product Thumbnail Image

ISO 14971: Understanding and Applying Risk Management

  • Training
  • 120 Minutes
  • Global
3-hr Virtual Seminar- Medical Device Adverse Event Reporting and Vigilance System During Clinical Trials and Post-Marketing: US, EU, and Canada - Product Thumbnail Image

3-hr Virtual Seminar- Medical Device Adverse Event Reporting and Vigilance System During Clinical Trials and Post-Marketing: US, EU, and Canada

  • Training
  • 3 Hours
  • Canada, United States, ... Canada, United States, Europe
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