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Industry Standards

Bullet-Proof CAPA - Product Thumbnail Image

Bullet-Proof CAPA

  • Training
  • 60 Minutes
  • Global
US FDA, Canada Health Canada, Brazil ANVISA, Australia TGA, Japan MHLW - MDSAP & EU ISO 13485 approach - Product Thumbnail Image

US FDA, Canada Health Canada, Brazil ANVISA, Australia TGA, Japan MHLW - MDSAP & EU ISO 13485 approach

  • Training
  • 60 Minutes
  • Australia, Brazil, ... Australia, Brazil, Canada, Japan, United States, Europe
Design Control / Ddesign and Development Requirements / Documents Under 21 CFR 820/ ISO 13485 7.3 - Product Thumbnail Image

Design Control / Ddesign and Development Requirements / Documents Under 21 CFR 820/ ISO 13485 7.3

  • Training
  • 90 Minutes
  • Global
ISO 9001:2015 Transition Overview - Product Thumbnail Image

ISO 9001:2015 Transition Overview

  • Training
  • 90 Minutes
  • Global
CAPA Investigations - Tools for a Compliant and Effective Investigation Process - Product Thumbnail Image

CAPA Investigations - Tools for a Compliant and Effective Investigation Process

  • Training
  • 60 Minutes
  • Global
Discussion of Revisions Contained in ISO 13485:2016 - Product Thumbnail Image

Discussion of Revisions Contained in ISO 13485:2016

  • Training
  • 90 Minutes
  • Global
Kaizen Approach to ISO 9001:2015 - Product Thumbnail Image

Kaizen Approach to ISO 9001:2015

  • Training
  • 90 Minutes
  • Global
Practical RCA and CAPA for the Food Industry - Tools, Methods and Documentation - Product Thumbnail Image

Practical RCA and CAPA for the Food Industry - Tools, Methods and Documentation

  • Training
  • 60 Minutes
  • Global
Overview of Changes in ISO 13485: 2016 - Product Thumbnail Image

Overview of Changes in ISO 13485: 2016

  • Training
  • 60 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
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
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
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
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
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
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
'Preventive Action' - the often ignored side of CAPA: Use FMEA to build preventive action into your CAPA program - Product Thumbnail Image

'Preventive Action' - the often ignored side of CAPA: Use FMEA to build preventive action into your CAPA program

  • Training
  • 60 Minutes
  • Global
Deviations and Process Failures within a CAPA program - Product Thumbnail Image

Deviations and Process Failures within a CAPA program

  • 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