+353-1-416-8900REST OF WORLD
+44-20-3973-8888REST OF WORLD
1-917-300-0470EAST COAST U.S
1-800-526-8630U.S. (TOLL FREE)

Search in Medical Devices returned 31,840 results.

Validation Essentials for Medical Device Manufacturers - IQ, OQ, PQ - Product Thumbnail Image

Validation Essentials for Medical Device Manufacturers - IQ, OQ, PQ

  • Training
  • 90 Minutes
  • Global
Medical Device Registration - Brazil and Argentina - Product Thumbnail Image

Medical Device Registration - Brazil and Argentina

  • Training
  • 90 Minutes
  • Argentina, Brazil
US FDA Medical Device QSR, 21 CFR 820 and Quality Management System - Product Thumbnail Image

US FDA Medical Device QSR, 21 CFR 820 and Quality Management System

  • Training
  • 90 Minutes
  • United States
EU ISO 13485:2016 Medical Device Quality Management System - Product Thumbnail Image

EU ISO 13485:2016 Medical Device Quality Management System

  • Training
  • 60 Minutes
  • Europe
Risk-based Design Control - The New Paradigm for Medical Device Design - Product Thumbnail Image

Risk-based Design Control - The New Paradigm for Medical Device Design

  • Training
  • 60 Minutes
  • Global
Effective Records Management and Document Control for Medical Devices - Product Thumbnail Image

Effective Records Management and Document Control for Medical Devices

  • Training
  • 60 Minutes
  • Global
Secure Medical Device Procurement - Product Thumbnail Image

Secure Medical Device Procurement

  • Training
  • 60 Minutes
  • Global
Understanding the Brazilian Regulatory Environment for Medical Devices - Product Thumbnail Image

Understanding the Brazilian Regulatory Environment for Medical Devices

  • Training
  • 60 Minutes
  • Brazil
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
How to Prepare for the New EU Medical Device Regulations - Product Thumbnail Image

How to Prepare for the New EU Medical Device Regulations

  • Training
  • 90 Minutes
  • Europe
Designing an Effective Cleaning Validation for Reusable Medical Devices in Today's Regulatory Environment - Product Thumbnail Image

Designing an Effective Cleaning Validation for Reusable Medical Devices in Today's Regulatory Environment

  • Training
  • 90 Minutes
  • Global
Regulatory Reporting: Building Systems and Processes to Ensure Compliance - Product Thumbnail Image

Regulatory Reporting: Building Systems and Processes to Ensure Compliance

  • Training
  • 60 Minutes
  • Global
How FDA trains its investigators to review CAPA and what should you do to prepare - Product Thumbnail Image

How FDA trains its investigators to review CAPA and what should you do to prepare

  • Training
  • 60 Minutes
  • Global
The Rush for ISO13485: 2016 - Product Thumbnail Image

The Rush for ISO13485: 2016

  • Training
  • 60 Minutes
  • Global
Overview of Medical Device Regulation in Europe - Product Thumbnail Image

Overview of Medical Device Regulation in Europe

  • Training
  • 90 Minutes
  • Europe
Root Cause Analysis and CAPA Controls for a Compliant Quality System - Product Thumbnail Image

Root Cause Analysis and CAPA Controls for a Compliant Quality System

  • Training
  • 60 Minutes
  • Global
Issues in Calibrations and Accuracy in Method Validation - Product Thumbnail Image

Issues in Calibrations and Accuracy in Method Validation

  • Training
  • 60 Minutes
  • Global
Classifying Medical Devices - US and EU - Product Thumbnail Image

Classifying Medical Devices - US and EU

  • Training
  • 60 Minutes
  • United States, Europe United States, Europe
Solutions for Addressing Fungal and Bacterial Spore Outbreaks in Pharmaceutical, Biotech, and Medical Device Operations - Product Thumbnail Image

Solutions for Addressing Fungal and Bacterial Spore Outbreaks in Pharmaceutical, Biotech, and Medical Device Operations

  • Training
  • 90 Minutes
  • Global
Introduction to Root Cause Investigation for CAPA - Product Thumbnail Image

Introduction to Root Cause Investigation for CAPA

  • Training
  • 60 Minutes
  • Global
Loading Indicator