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16949
Overview: Transitioning from ISO/TS to IATF 16949:2016
Overview Courses & Certificate Subscription Plans
IATF 16949 Overview Lessons
Transition Tests & Content
Failure Mode & Effects Analysis (FMEA)
IATF 16949:2016 Internal Auditor Courses
Internal Auditor Courses & Certificate Subscription
Module 1 Lessons
Module 2 Lessons
Module 3 Lessons
Module 4 Lessons
Module 5 Lessons
Module 6 Lessons
List of all Internal Auditor lessons, tests and downloads
IATF 16949: 2016 Sanctioned Interpretations Discussed
IATF 16949 for Process Owners
9001
Online courses for the ISO 9001:2015 Standard
Overview Course for ISO 9001:2015
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13485
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16949
IATF 16949:2016
is the global technical specification and quality management standard for the automotive industry. Based on ISO 9001:2015, it replaces ISO/TS 16949. It is designed to be used in conjunction with ISO 9001:2015 and contains supplemental requirements specific to the automotive industry.
Overview: Transitioning from ISO/TS to IATF 16949:2016
Overview Courses & Certificate Subscription Plans
IATF 16949 Overview Lessons
Transition Tests & Content
Failure Mode & Effects Analysis (FMEA)
IATF 16949:2016 Internal Auditor Courses
Internal Auditor Courses & Certificate Subscription
Module 1 Lessons
Module 2 Lessons
Module 3 Lessons
Module 4 Lessons
Module 5 Lessons
Module 6 Lessons
List of all Internal Auditor lessons, tests and downloads
IATF 16949: 2016 Sanctioned Interpretations Discussed
IATF 16949 for Process Owners
9001
ISO 9001:2015
is the international standard specifying requirements for a quality management system (QMS). Organizations use the standard to show the ability to provide products and services that meet customer and regulatory requirements.
Online courses for the ISO 9001:2015 Standard
Overview Course for ISO 9001:2015
ISO 9001:2015 Internal Auditor
Risk Requirements for ISO 9001:2015
Related Courses to help you with your QMS
ISO 19011 - Auditing Management Systems
Effective Corrective Actions
Creating the Audit Check List
Getting the Audit Started
Conducting the Audit
SIPOC Lessons
Turtle Diagrams
Classifying Non-Conformances
Root Cause Analysis
Project Management
Process Approach
13485
ISO 13485:2016
Medical devices – Quality management systems – Requirements for regulatory purposes, is an internationally agreed standard that sets out the requirements for a quality management system specific to the medical devices industry. It has recently been revised, with the new version published in March 2016. Our courses are designed to help you during the transition.
ISO 13485 Online Course
ISO 13485 Overview & Internal Auditing Course
14001
ISO 14001:2015
is the international standard that specifies requirements for an effective environmental management system (EMS). It encourages improved environmental performance and is a useful tool to comply with government environmental regulations.
ISO 14001:2015 Online Courses
ISO 14001 Internal Auditor Training
ISO 14001:2015 Overview
ISO 19011 - Auditing Management Systems
AS9100D
AS9100D
Prepared by the International Aerospace Quality Group (IAQG), with representatives from aviation, space, and defense companies in the Americas, Asia/Pacific and Europe, AS9100:2016/AS9100D standardizes quality management system requirements.
AS9100D Internal Auditing
AS9100D Course
45001
ISO 45001 Courses
ISO 45001 Internal Auditing Courses
Related Courses
ISO 19011 - Auditing Management Systems
Effective Corrective Actions
ISO 45001:2018
The standard is based on requirements to help organizations help by by providing a framework to improve employee safety, reduce workplace risks and create better, safer working conditions, all over the world.
The standard was developed by a committee of occupational health and safety experts, and follows other generic management system approaches such as ISO 14001 and ISO 9001.
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16949
Overview: Transitioning from ISO/TS to IATF 16949:2016
Transition Tests & Content
IATF 16949 Internal Auditor Tests & Content
List of articles in category General Transistion
Title
Lessons for Overview - IATF 16949:2016
Overview Transition Test & Certificate
16949 Transition Lessons
S001 - Opening
S002 - Getting Started
S003 - Thoughts for us to consider…
S004 - Presentation information
S005 - Section 4.3.1: Determining the scope of the quality management system – supplemental
S006 - Section 4.3.2: Customer-specific requirements
S007 - Section 4.4.1.1: Conformance of products and processes
S008 - Section 4.4.1.2: Product Safety
S009 - Section 4.4.1.2: Product Safety
S010 - Section 5.1.1.1: Corporate Responsibility
S011 - Section 5.1.1.2: Process effectiveness & efficiency
S012 - Section 5.1.1.3: Process Owners
S013 - Section 5.3.1: Organizational roles, responsibilities, & authorities – supplemental
S014 - Section 5.3.2: Responsibility and authority for product requirements and corrective actions
S015 - Section 6.1.2.1: Risk Analysis
S016 - Section 6.1.2.2: Preventive action
S017 - Section 6.1.2.3: Contingency Plans
S018 - Section 6.2.2.1: Quality objectives and planning to achieve them – supplemental
S019 - Section 7.1.3.1: Plant, facility, and equipment planning
S020 - Section 7.1.5.1.1: Measurement system analysis
S021 - Section 7.1.5.2.1: Calibration/verification records
S022 - Section 7.1.5.2.1: Calibration/verification records
S023 - Section 7.1.5.3.2: External laboratory
S024 - Section 7.2.1: Competence – supplemental
S025 - Section 7.2.2: Competence – on-the-job training
S026 - Section 7.2.3: Internal auditor competency
S027 - Section 7.2.3: Internal auditor competency
S028 - Section 7.2.4: Second-party auditor competency
S029 - Section 7.3.1: Awareness – supplemental
S030 - Section 7.3.2: Employee motivation and empowerment
S031 - Section 7.5.1.1: Quality management system documentation
S032 - Section 7.5.3.2.1: Record retention
S033 - Section 7.5.3.2.2: Engineering specifications
S034 - Section 8.1.1: Operational planning and control — supplemental
S035 - Section 8.2.1.1: Customer communication — supplemental
S036 - Section 8.2.2.1: Determining the requirements for products and services – supplemental
S037 - Section 8.2.3.1.1: Review of the requirements for products and services — supplemental
S038 - Section 8.2.3.1.3: Organization manufacturing feasibility
S039 - Section 8.3.1.1: Design and development of products and services – supplemental
S040 - Section 8.3.2.1: Design and development planning – supplemental
S041 - Section 8.3.2.3: Development of products with embedded software
S042 - Section 8.3.3.1: Product design input
S043 - Section 8.3.3.2: Manufacturing process design input
S044 - Section 8.3.3.3: Special characteristics
S045 - Section 8.3.4.1: Monitoring
S046 - Section 8.3.4.2: Design and development validation
S047 - Section 8.3.4.3: Prototype program
S048 - Section 8.3.4.4: Product approval process
S049 - Section 8.3.5.1: Design and development outputs – supplemental (Outputs as applicable)
S050 - Section 8.3.5.2: Manufacturing process design output
S051 - Section 8.3.5.2: Manufacturing process design output
S052 - Section 8.3.6.1: Design and development changes – supplemental
S053 - Section 8.4.1.1: General - supplemental (under Control of externally provided processes, products and services)
S054 - Section 8.4.1.2: Supplier selection process
S055 - Section 8.4.1.3: Customer-directed sources (also known as “Directed–Buy”)
S056 - Section 8.4.2.1: Type and extent of control – supplemental
S057 - Section 8.4.2.2: Statutory and regulatory requirements
S058 - Section 8.4.2.3: Supplier quality management system development
S059 - Section 8.4.2.3.1: Automotive product-related software / automotive products with embedded SW
S060 - Section 8.4.2.4: Supplier monitoring
S061 - Section 8.4.2.4: Supplier monitoring
S062 - Section 8.4.2.4.1: Second-party audits
S063 - Section 8.4.2.5: Supplier development
S064 - Section 8.4.3.1: Information for external providers – supplemental
S065 - Section 8.5.1.1: Control plan
S066 - Section 8.5.1.1: Control plan (continued)
S067 - Section 8.5.1.1: Control plan (continued)
S068 - Section 8.5.1.2: Standardized work – operator instructions and visual standards
S069 - Section 8.5.1.3: Verification of job set-ups
S070 - Section 8.5.1.4: Verification after shutdown
S071 - Section 8.5.1.5: Total productive maintenance
S072 - Section 8.5.1.6: Management of prod. tooling and manufacturing, test, inspection tooling and equipment
S073 - Section 8.5.1.6: Management of prod. tooling and mfg., test, inspection tooling and equipment
S074 - Section 8.5.1.7: Production scheduling
S075 - Section 8.5.2.1: Identification and traceability — supplemental
S076 - Section 8.5.2.1: Identification and traceability — supplemental
S077 - Section 8.5.4.1: Preservation – supplemental
S078 - Section 8.5.4.1: Preservation – supplemental
S079 - Section 8.5.5.1: Feedback of information from service
S080 - Section 8.5.5.2: Service agreement with customer
S081 - Section 8.5.6.1: Control of changes – supplemental
S082 - Section 8.5.6.1: Control of changes – supplemental
S083 - Section 8.5.6.1.1: Temporary change of process controls
S084 - Section 8.5.6.1.1: Temporary change of process controls (Continued)
S085 - Section 8.6.1: Release of products and services — supplemental
S086 - Section 8.6.2: Layout inspection and functional testing
S087 - Section 8.6.3: Appearance items
S088 - Section 8.6.4: Verification & acceptance of conformity of externally provided products & services
S089 - Section 8.6.5: Statutory and regulatory conformity
S090 - Section 8.7.1.1: Customer authorization for concession
S091 - Section 8.7.1.2: Control of nonconforming product – customer specified process
S092 - Section 8.7.1.3: Control of suspect product
S093 - Section 8.7.1.4: Control of reworked product
S094 - Section 8.7.1.5: Control of repaired product
S095 - Section 8.7.1.6: Customer notification
S096 - Section 8.7.1.7: Nonconforming product disposition
S097 - Section 9.1.1.1: Monitoring and measurement of manufacturing processes
S098 - Section 9.1.1.1: Monitoring and measurement of manufacturing processes
S099 - Section 9.1.1.2: Identification of statistical tools
S100 - Section 9.1.1.3: Application of statistical concepts
S101 - Section 9.1.2.1: Customer satisfaction – supplemental
S102 - Section 9.1.3.1: Prioritization
S103 - Section 9.2.2.1: Internal audit program
S104 - Section 9.2.2.2: Quality management system audit
S105 - Section 9.2.2.3: Manufacturing process audit
S106 - Section 9.2.2.4: Product audit
S107 - Section 9.3.1.1: Management review – supplemental
S108 - Section 9.3.2.1: Management review inputs – supplemental
S109 - Section 9.3.3.1: Management review outputs – supplemental
S110 - Section 10.2.3: Problem solving
S111 - Section 10.2.4: Error-proofing
S112 - Section 10.2.5: Warranty management systems
S113 - Section 10.2.6: Customer complaints and field failure test analysis
S114 - Section 10.3.1: Continual improvement – supplemental
S115 - Thoughts for us to consider…
S116 - Next Steps & Closing
S999 - Transition Overview Test and Competence Certificate
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