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Search in Medical Devices returned 31,629 results.

The FDA's final Medical Device Data System (MDDS) rule and its implications for currently regulated and unregulated vendors and providers - Product Thumbnail Image

The FDA's final Medical Device Data System (MDDS) rule and its implications for currently regulated and unregulated vendors and providers

  • Training
  • 65 Minutes
  • Global
Design for Six Sigma in Medical Devices: Integration with the FDA Quality Systems Regulations - Product Thumbnail Image

Design for Six Sigma in Medical Devices: Integration with the FDA Quality Systems Regulations

  • Training
  • 60 Minutes
  • Global
Internal Auditing Essentials for Medical Device Manufacturers to comply with FDA QSR and ISO13485 - Product Thumbnail Image

Internal Auditing Essentials for Medical Device Manufacturers to comply with FDA QSR and ISO13485

  • Training
  • 60 Minutes
  • Global
Effectively application of FMEA as a Risk Management Tool and meet ISO 13485:2003 Risk Management (ISO 14971) Requirements - Product Thumbnail Image

Effectively application of FMEA as a Risk Management Tool and meet ISO 13485:2003 Risk Management (ISO 14971) Requirements

  • Training
  • 60 Minutes
  • Global
Bringing Compliance to Design Control through Life Cycle Management of Older Medical Devices and Surgical Instruments - Product Thumbnail Image

Bringing Compliance to Design Control through Life Cycle Management of Older Medical Devices and Surgical Instruments

  • Training
  • 60 Minutes
  • Global
International GMP's for Medical Devices: Quality System requirements for USA, Europe, Canada and Japan - Product Thumbnail Image

International GMP's for Medical Devices: Quality System requirements for USA, Europe, Canada and Japan

  • Training
  • Canada, Japan, United States, ... Canada, Japan, United States, Europe, Global
Mobile Apps as Medical Devices - Product Thumbnail Image

Mobile Apps as Medical Devices

  • Training
  • 60 Minutes
  • Global
ISO 14971:2019 - Does your Risk Analysis meet this new revision of the Standard? - Product Thumbnail Image

ISO 14971:2019 - Does your Risk Analysis meet this new revision of the Standard?

  • Training
  • 60 Minutes
  • Global
Sterilization of Pharmaceutical Products and Medical Devices - Product Thumbnail Image

Sterilization of Pharmaceutical Products and Medical Devices

  • Training
  • 60 Minutes
  • Global
New European Medical Device Regulation (MDR) 2017-745 - Product Thumbnail Image

New European Medical Device Regulation (MDR) 2017-745

  • Training
  • 60 Minutes
  • Europe
Bullet-Proof CAPA - Product Thumbnail Image

Bullet-Proof CAPA

  • Training
  • 60 Minutes
  • Global
CDISC Mapping 5: ADAM Models - ADSL, BDS and ADAE - Product Thumbnail Image

CDISC Mapping 5: ADAM Models - ADSL, BDS and ADAE

  • Training
  • 90 Minutes
  • Global
CDISC Mapping 4: SDTMs and ADAMs Examples (80%/20% Mapping Rule) - Product Thumbnail Image

CDISC Mapping 4: SDTMs and ADAMs Examples (80%/20% Mapping Rule)

  • Training
  • 90 Minutes
  • Global
CDISC Mapping 3: Compare and Contrast SDTM and ADaM Steps - Product Thumbnail Image

CDISC Mapping 3: Compare and Contrast SDTM and ADaM Steps

  • Training
  • 90 Minutes
  • Global
Reprocessing Reusable Medical Devices - Cleaning and Labeling Requirements - Product Thumbnail Image

Reprocessing Reusable Medical Devices - Cleaning and Labeling Requirements

  • Training
  • 60 Minutes
  • Global
Risk Management for Medical Devices: ISO 14971:2007 - Product Thumbnail Image

Risk Management for Medical Devices: ISO 14971:2007

  • Training
  • 75 Minutes
  • Global
Corrective And Preventive Action: CAPA-A Risk Mitigating Quality System - Product Thumbnail Image

Corrective And Preventive Action: CAPA-A Risk Mitigating Quality System

  • Training
  • 60 Minutes
  • Global
Contamination Control 101 in Pharmaceutical, Biotech, and Medical Device Clean rooms - Product Thumbnail Image

Contamination Control 101 in Pharmaceutical, Biotech, and Medical Device Clean rooms

  • Training
  • 90 Minutes
  • Global
The IDE (Investigational Device Exemption) - It's Purpose and Preparation - Product Thumbnail Image

The IDE (Investigational Device Exemption) - It's Purpose and Preparation

  • Training
  • 60 Minutes
  • Global
Basic Requirements for Steam Sterilizer Validation per ISO 17665 - Product Thumbnail Image

Basic Requirements for Steam Sterilizer Validation per ISO 17665

  • Training
  • 60 Minutes
  • Global
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