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Results for tag: "Medical Device Manufacturer"

New Medical Device Vigilance Guidelines - Product Thumbnail Image

New Medical Device Vigilance Guidelines

  • Training
  • 60 Minutes
  • Global
Changes to the Medical Devices Directive: 93/42/EEC - Product Thumbnail Image

Changes to the Medical Devices Directive: 93/42/EEC

  • 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
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
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
How to Create Clinical Evaluation According to EU MDR 2017/745 Article 61 and Annex XIV - Product Thumbnail Image

How to Create Clinical Evaluation According to EU MDR 2017/745 Article 61 and Annex XIV

  • Training
  • 75 Minutes
  • Europe
Validation for Medical Device Manufacturers - Master IQ, OQ, PQ - Product Thumbnail Image

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

  • Training
  • 90 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
Medical IT Device Security: Why Medical Device Manufacturers Must Take the Lead and Drive Regulatory Compliance - Product Thumbnail Image

Medical IT Device Security: Why Medical Device Manufacturers Must Take the Lead and Drive Regulatory Compliance

  • Training
  • 60 Minutes
  • Global
The Revision of the Medical Devices Directive 93/42/EEC, Background, Proposal and What It Means - Product Thumbnail Image

The Revision of the Medical Devices Directive 93/42/EEC, Background, Proposal and What It Means

  • Training
  • 60 Minutes
  • Global
FDA Regulation, 3D Printing and Medical Devices - Product Thumbnail Image

FDA Regulation, 3D Printing and Medical Devices

  • Training
  • 75 Minutes
  • Global
FDA's New Endotoxin Test Guidance for Human Parenteral Drugs, Biological Products and Medical Devices - Product Thumbnail Image

FDA's New Endotoxin Test Guidance for Human Parenteral Drugs, Biological Products and Medical Devices

  • Training
  • 90 Minutes
  • Global
Overview of the Medical Device Risk Management Standard-ISO 14971 - Product Thumbnail Image

Overview of the Medical Device Risk Management Standard-ISO 14971

  • Training
  • 90 Minutes
  • Global
US FDA 510(k): Best Practices for 510(k) Preparation and Submission - Product Thumbnail Image

US FDA 510(k): Best Practices for 510(k) Preparation and Submission

  • Training
  • 60 Minutes
  • United States
Process Validation for Medical Device Manufacturers - Product Thumbnail Image

Process Validation for Medical Device Manufacturers

  • Training
  • 90 Minutes
  • Global
ISO 13485 - Medical Devices: Quality Management Systems - Product Thumbnail Image

ISO 13485 - Medical Devices: Quality Management Systems

  • Training
  • 90 Minutes
  • Global
An Easy to Implement Integrated Risk Management Approach Compliant with ISO 14971 - Product Thumbnail Image

An Easy to Implement Integrated Risk Management Approach Compliant with ISO 14971

  • Training
  • 60 Minutes
  • Global
The Use and Mis-use of FMEA in Medical Device Risk Management - Product Thumbnail Image

The Use and Mis-use of FMEA in Medical Device Risk Management

  • Training
  • 60 Minutes
  • Global
Strategies for an Effective Root Cause Analysis and CAPA Program - Product Thumbnail Image

Strategies for an Effective Root Cause Analysis and CAPA Program

  • Training
  • 60 Minutes
  • Global
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The Medical Device Manufacturer market is a highly competitive industry that produces a wide range of products used in the diagnosis, treatment, and prevention of medical conditions. These products range from simple instruments such as syringes and thermometers to complex devices such as pacemakers and artificial organs. Medical device manufacturers must adhere to strict regulations and standards set by the Food and Drug Administration (FDA) in order to ensure the safety and efficacy of their products. Medical device manufacturers are typically large, multinational corporations that have the resources to invest in research and development, as well as the necessary infrastructure to produce and distribute their products. They often collaborate with healthcare providers, universities, and other organizations to develop innovative products and technologies. Some of the major players in the Medical Device Manufacturer market include Johnson & Johnson, Medtronic, Stryker, Philips, and Becton Dickinson. Show Less Read more