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Industry Standards

ISO 45001 - Migration Essentials - Parts 1, 2 and 3 - Product Thumbnail Image

ISO 45001 - Migration Essentials - Parts 1, 2 and 3

  • Training
  • 180 Minutes
  • Global
OSHA's Famous Top 10 List of Citations: General Industry and Construction Industry Standards - Product Thumbnail Image

OSHA's Famous Top 10 List of Citations: General Industry and Construction Industry Standards

  • Training
  • 60 Minutes
  • Global
Navigating the New FDA Draft Guidance on ISO 10993: Biological Evaluation of Medical Devices - Product Thumbnail Image

Navigating the New FDA Draft Guidance on ISO 10993: Biological Evaluation of Medical Devices

  • Training
  • 60 Minutes
  • Global
Understanding ISO 13485 and its Relation to FDA's Quality Systems Regulation - Product Thumbnail Image

Understanding ISO 13485 and its Relation to FDA's Quality Systems Regulation

  • Training
  • 90 Minutes
  • Global
How to conduct Risk Assessments as per ISO 31000/31010(SOX) - Product Thumbnail Image

How to conduct Risk Assessments as per ISO 31000/31010(SOX)

  • Training
  • 90 Minutes
  • Global
Integrating Risk Management into the CAPA System - Product Thumbnail Image

Integrating Risk Management into the CAPA System

  • 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
Document Approval, Control, and Distribution: How to Meet FDA QSR and ISO 13485 Requirements - Product Thumbnail Image

Document Approval, Control, and Distribution: How to Meet FDA QSR and ISO 13485 Requirements

  • Training
  • 60 Minutes
  • Global
Making the Move to ISO 27001: 2013 - Product Thumbnail Image

Making the Move to ISO 27001: 2013

  • Training
  • 90 Minutes
  • Global
How to Avoid an FDA Warning Letter with a Strong CAPA Program - Product Thumbnail Image

How to Avoid an FDA Warning Letter with a Strong CAPA Program

  • Training
  • 60 Minutes
  • Global
ISO 22000 vs GFSI (SQF, BRC, IFS, and FSSC 22000): Meeting key Requirements - Product Thumbnail Image

ISO 22000 vs GFSI (SQF, BRC, IFS, and FSSC 22000): Meeting key Requirements

  • Training
  • 60 Minutes
  • Global
How to respond to GXP (GCP, GLP, GMP, GPV) Inspection and Audit Findings using Correction and Preventative Action (CAPA) - Product Thumbnail Image

How to respond to GXP (GCP, GLP, GMP, GPV) Inspection and Audit Findings using Correction and Preventative Action (CAPA)

  • Training
  • 60 Minutes
  • Global
Understanding ISO 13485 vs. ISO 9001 for Successful QMS in Medical Device Industries - Product Thumbnail Image

Understanding ISO 13485 vs. ISO 9001 for Successful QMS in Medical Device Industries

  • 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
ISO 13485:2003 - A Straightforward Interpretation with Recommendations for Easy Implementation - Product Thumbnail Image

ISO 13485:2003 - A Straightforward Interpretation with Recommendations for Easy Implementation

  • Training
  • 90 Minutes
  • Global
How CAPA and complaint handling should interact in Medical Device - Simplification of the processes is often needed to preserve their effectiveness - Product Thumbnail Image

How CAPA and complaint handling should interact in Medical Device - Simplification of the processes is often needed to preserve their effectiveness

  • Training
  • 60 Minutes
  • Global
Root Cause Analysis for CAPA Management (Shutting Down the Alligator Farm) - Product Thumbnail Image

Root Cause Analysis for CAPA Management (Shutting Down the Alligator Farm)

  • Training
  • 60 Minutes
  • Global
Japanese PAL - JPAL QMS requirements in Ordinance 169 and differences to ISO 13485 - Product Thumbnail Image

Japanese PAL - JPAL QMS requirements in Ordinance 169 and differences to ISO 13485

  • Training
  • 90 Minutes
  • Japan
How to Internal Audit to ISO 9001:2008 - Product Thumbnail Image

How to Internal Audit to ISO 9001:2008

  • Training
  • 60 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
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Industry Standards are a set of guidelines, protocols, and best practices that are used by companies in a particular industry. These standards are designed to ensure that products and services are of a consistent quality and meet the needs of customers. Companies that adhere to industry standards are able to maintain a competitive edge in the market. Industry Standards are developed by industry associations, government agencies, and other organizations. They are often based on research and feedback from industry experts. Companies must adhere to these standards in order to remain competitive and compliant with regulations. Examples of companies that adhere to industry standards include Apple, Microsoft, Amazon, and Google. These companies have established themselves as leaders in their respective industries by adhering to industry standards. They have also been able to maintain their competitive edge by consistently meeting customer expectations. Show Less Read more