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Industry Standards

ISO 14971:2007 -- The Newly Revised Risk Management Standard for Medical Products - Product Thumbnail Image

ISO 14971:2007 -- The Newly Revised Risk Management Standard for Medical Products

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

ISO 13485 - Medical Devices: Quality Management Systems

  • Training
  • 90 Minutes
  • Global
ISO 14001: Complete Overview, Implementation and Compliance - Product Thumbnail Image

ISO 14001: Complete Overview, Implementation and Compliance

  • Training
  • 120 Minutes
  • Global
ISO 14971: Understanding and Applying Risk Management - Product Thumbnail Image

ISO 14971: Understanding and Applying Risk Management

  • Training
  • 120 Minutes
  • Global
(QMS) Competence and Training Requirements per FDA QSR and ISO 13485 - Product Thumbnail Image

(QMS) Competence and Training Requirements per FDA QSR and ISO 13485

  • Training
  • 90 Minutes
  • Global
Medical Device Risk Management Using ISO 14971 - Product Thumbnail Image

Medical Device Risk Management Using ISO 14971

  • Training
  • 90 Minutes
  • Global
Gamma Sterilizer Validation: Method 1 and VDmax25 per ISO 11137 - Product Thumbnail Image

Gamma Sterilizer Validation: Method 1 and VDmax25 per ISO 11137

  • Training
  • 60 Minutes
  • Global
Training Requirements and Practices to Assure QSR and ISO Compliance - Product Thumbnail Image

Training Requirements and Practices to Assure QSR and ISO Compliance

  • Training
  • 60 Minutes
  • Global
Five Steps in Conducting Audits - ISO 19011 - Product Thumbnail Image

Five Steps in Conducting Audits - ISO 19011

  • Training
  • 60 Minutes
  • Global
Management Controls needed for an effective QMS to meet FDA QSR and ISO 13485 regulations - Product Thumbnail Image

Management Controls needed for an effective QMS to meet FDA QSR and ISO 13485 regulations

  • Training
  • 60 Minutes
  • Global
From CAPA to Capability: Shifting the Focus to Profitability - Product Thumbnail Image

From CAPA to Capability: Shifting the Focus to Profitability

  • Training
  • 60 Minutes
  • Global
CAPA Essentials - core principles and practices needed to implement an effective and efficient CAPA process - Product Thumbnail Image

CAPA Essentials - core principles and practices needed to implement an effective and efficient CAPA process

  • 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
Supplier Evaluation and Internal Auditing for FDA and ISO 13485 Compliance: Pack of Three Courses - Product Thumbnail Image

Supplier Evaluation and Internal Auditing for FDA and ISO 13485 Compliance: Pack of Three Courses

  • Training
  • Global
Validation for FDA and ISO 13485 Compliance: Pack of Two Courses - Product Thumbnail Image

Validation for FDA and ISO 13485 Compliance: Pack of Two Courses

  • Training
  • Global
Implementing an Environmental Management System to ISO 14001 - Product Thumbnail Image

Implementing an Environmental Management System to ISO 14001

  • Training
  • 60 Minutes
  • Global
CAPA - Best Practices and Common Pitfalls for FDA Regulated Industries - Product Thumbnail Image

CAPA - Best Practices and Common Pitfalls for FDA Regulated Industries

  • Training
  • 60 Minutes
  • Global
Setting up a QSR Compliant CAPA System - Product Thumbnail Image

Setting up a QSR Compliant CAPA System

  • Training
  • 60 Minutes
  • Global
Review of Changes to the New ANSI/AAMI/ISO 11137-2006 (Parts 1, 2, & 3) Sterilization of health care products - requirements for validation and routine control - Radiation Sterilization - Product Thumbnail Image

Review of Changes to the New ANSI/AAMI/ISO 11137-2006 (Parts 1, 2, & 3) Sterilization of health care products - requirements for validation and routine control - Radiation Sterilization

  • Training
  • 60 Minutes
  • Global
Best Practices on Six Sigma and CAPA Convergence - Product Thumbnail Image

Best Practices on Six Sigma and CAPA Convergence

  • 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