1.6 Management Systems
1.6.1 ISO 9001:2015 Quality Management Principles
ISO 9001:2015 Quality Management Principles
Overview:
This course explores the fundamental principles of ISO 9001:2015, which focus on continual performance improvement through understanding and addressing customer needs while promoting business excellence throughout the organization. Participants will gain insight into the foundational concepts and requirements of the current ISO 9001:2015 standard, including risk-based thinking, leadership engagement, and the process approach to quality management. This course is ideal for individuals interested in the evolution of ISO 9001 and professionals involved in quality management systems or quality assurance practices.
Key Benefits:
- Understand the core principles of ISO 9001:2015 and their role in quality management
- Learn how to implement a quality management system that meets current standards
- Enhance your ability to drive continual improvement within your organization
Course Objectives:
- Gain a comprehensive understanding of ISO 9001:2015 principles
- Explore the relationship between customer satisfaction and quality management
- Learn how to apply the principles of ISO 9001:2015 to improve organizational performance
Duration:
16 hours
Certification Notes:
Participants will receive a course completion certificate upon successful completion.
Enrollment:
Click the "Send a Request" button below to learn more about the courses and schedule
a consultation with our expert.
1.6.2 ISO 45001:2018 Occupational Health and Safety Management System (OHSMS) Implementation
ISO 45001:2018 Occupational Health and Safety Management System (OHSMS) Implementation
Overview:
This course offers detailed training on the ISO 45001:2018 Occupational Health and Safety Management System (OHSMS) standard. Designed to help organizations improve workplace safety, reduce risks, and enhance overall health and safety performance, ISO 45001:2018 provides a systematic approach to managing health and safety risks.
Participants will learn how to identify potential hazards, assess risks, and implement effective safety measures. The course also covers regulatory compliance at local, state, and national levels, helping organizations create a safer and more responsible workplace. The course ensures organizations can achieve certification and realize a return on investment through better resource management and compliance.
Key Benefits:
- Improve workplace safety and reduce occupational risks
- Gain insight into ISO 45001:2018 requirements and implementation strategies
- Enhance compliance with health and safety regulations
- Foster a proactive health and safety culture within the organization
Course Objectives:
- Understand the structure and requirements of ISO 45001:2018
- Learn how to identify hazards, assess risks, and implement safety measures
- Develop a plan to prepare for ISO 45001:2018 audits and certification
Duration:
16 hours
Certification Notes:
Participants will receive a course completion certificate upon successful completion.
Enrollment:
Click the "Send a Request" button below to learn more about the courses and schedule
a consultation with our expert.
1.6.3 ISO 14001:2015 Environmental Management System (EMS) Implementation
ISO 14001:2015 Environmental Management System (EMS) Implementation
Overview:
This course provides comprehensive training and hands-on assistance to help companies implement and become certified to the ISO 14001:2015 Environmental Management System (EMS) standard within one year, even with no prior experience. ISO 14001:2015 helps organizations detect and reduce waste in resources and processes, leading to significant cost savings and improved environmental performance. The course covers compliance with local, state, and national environmental regulations, assisting companies in meeting their regulatory obligations.
Participants will learn how to identify and prioritize environmental aspects – factors that can impact the environment – and develop action plans to mitigate or eliminate those impacts. The course ensures organizations can achieve certification and realize a return on investment through better resource management and compliance.
Key Benefits:
- Prepare for ISO 14001:2015 implementation with hands-on guidance
- Identify environmental aspects and create action plans to reduce environmental impact
- Improve compliance with local, state, and national environmental regulations
- Reduce resource waste and increase operational efficiency
Course Objectives:
- Learn the key requirements of ISO 14001:2015
- Develop an action plan for reducing environmental risks and impacts
- Prepare for a successful ISO 14001:2015 certification audit
Duration:
16 hours
Certification Notes:
Participants will receive a course completion certificate upon successful completion.
Enrollment:
Click the "Send a Request" button below to learn more about the courses and schedule
a consultation with our expert.
1.6.4 ISO 13485:2016 Medical Devices Quality Management System (QMS) Implementation
ISO 13485:2016 Medical Devices Quality Management System (QMS) Implementation
Overview:
This course provides a comprehensive understanding of the ISO 13485:2016 standard, which focuses on establishing a robust Quality Management System (QMS) for the medical device industry. Participants will learn the key requirements of ISO 13485:2016, including risk management, process controls, and regulatory compliance. The course covers the essential aspects of implementing a QMS that ensures product quality and patient safety throughout the product lifecycle.
This training is designed to help medical device manufacturers align their operations with ISO 13485:2016. The course ensures organizations can achieve certification and realize a return on investment through better resource management and compliance.
Key Benefits:
- Understand ISO 13485:2016 requirements for medical devices
- Improve product quality and ensure patient safety
- Gain insights into risk management and process controls
- Enhance compliance with global medical device regulations
Course Objectives:
- Learn how to implement ISO 13485:2016 for medical devices
- Identify and mitigate risks associated with medical device manufacturing
- Prepare for audits and certification by understanding key ISO 13485:2016 processes and requirements
Duration:
16 hours
Certification Notes:
Participants will receive a course completion certificate upon successful completion.
Enrollment:
Click the "Send a Request" button below to learn more about the courses and schedule
a consultation with our expert.
1.6.5 ISO/IEC 17001: Implementation of Conformity Assessment – General Requirements
ISO/IEC 17001: Implementation of Conformity Assessment – General Requirements
Overview:
This course provides an in-depth understanding of ISO/IEC 17001, focusing on implementing conformity assessment frameworks. Participants will learn the fundamental requirements of the standard, designed to ensure consistent, reliable, and transparent conformity assessment practices. The course covers the principles for managing impartiality, confidentiality, and competence for bodies performing conformity assessment activities. It is ideal for professionals working with accreditation bodies or organizations seeking to enhance their internal compliance frameworks.
The course ensures organizations can achieve certification and realize a return on investment through better resource management and compliance.
Key Benefits:
- Gain a solid understanding of ISO/IEC 17001 conformity assessment principles
- Learn how to manage impartiality and confidentiality in assessment processes
- Ensure competence in conformity assessments for consistent outcomes
- Enhance transparency and credibility in organizational assessments
Course Objectives:
- Understand the requirements of ISO/IEC 17001 for conformity assessments
- Prepare for internal or third-party assessments aligned with ISO/IEC 17001
- Identify best practices for managing compliance, impartiality, and confidentiality
Duration:
Varies depending on organizational requirements
Certification Notes:
Participants will receive a course completion certificate after successful completion
Enrollment:
Click the "Send a Request" button below to learn more about the courses and schedule
a consultation with our expert.
1.6.6 AS9100D (Aerospace) – Quality Management System
AS9100D (Aerospace) – Quality Management System
Overview:
This detailed course is designed to provide participants with the knowledge and skills to perform effective internal audits based on AS9100D (Aerospace Quality Management Systems), which is built upon the ISO 9001:2015 framework with additional requirements specific to the aerospace industry. Participants will learn about auditing practices according to ISO 19011, including the phases of audit planning, execution, reporting, and follow-up. Special focus will be placed on the aerospace-specific aspects of AS9100D, such as risk management, product safety, and counterfeit part prevention.
This course is ideal for professionals who manage, conduct, or participate in internal audits for organizations involved in the aerospace sector and those preparing for AS9100D certification. The training will ensure participants are well-prepared for external audits and able to identify areas for improvement within their organization.
Key Benefits:
- Gain in-depth knowledge of AS9100D aerospace quality management system requirements
- Learn how to conduct, document, and report internal audits according to ISO 19011
- Develop a strong understanding of aerospace-specific requirements, including risk management and product safety
- Enhance your organization's readiness for AS9100D certification
Course Objectives:
- Learn to audit for compliance with AS9100D and ISO 9001:2015
- Understand how to apply ISO 19011 audit standards to aerospace QMS
- Identify non-conformities and drive continuous improvement within your organization
Duration:
16 hours
Certification Notes:
Participants will receive a course completion certificate upon successful completion.
Enrollment:
Click the "Send a Request" button below to learn more about the courses and schedule
a consultation with our expert.
1.6.7 IATF 16949:2016 (Automotive) – Quality Management System
IATF 16949:2016 (Automotive) – Quality Management System
Overview:
This comprehensive course is designed to equip participants with the skills and knowledge required to conduct effective internal audits based on the IATF 16949:2016 standard, which is tailored to the automotive industry. Built upon the ISO 9001:2015 framework, IATF 16949:2016 includes additional requirements that address the complexities of automotive manufacturing. Participants will learn about auditing practices in line with ISO 19011, covering key phases such as audit planning, execution, reporting, and follow-up. The course will also emphasize automotive-specific areas like risk management, defect prevention, and continuous improvement.
This course is ideal for professionals involved in internal audits, quality management, or those preparing their organizations for IATF 16949:2016 certification. It ensures that participants are well-prepared for external audits and able to enhance quality management within their organizations.
Key Benefits:
- Gain in-depth understanding of IATF 16949:2016 automotive quality management system
requirements
- Learn how to conduct, document, and report internal audits according to ISO 19011
- Master automotive-specific requirements such as risk management, defect prevention,
and continuous improvement
- Improve organizational readiness for IATF 16949:2016 certification
Course Objectives:
- Learn to audit for compliance with IATF 16949:2016 and ISO 9001:2015
- Understand how to apply ISO 19011 audit standards to the automotive industry
- Identify non-conformities and drive continuous improvement within your organization
Duration:
16 hours
Certification Notes:
Participants will receive a course completion certificate upon successful completion.
Enrollment:
Click the "Send a Request" button below to learn more about the courses and schedule
a consultation with our expert.
1.6.8 Internal Auditor: AS9100D (Aerospace), IATF 16949:2016 (Automotive), ISO/IEC 17001, ISO 13485:2016, ISO 9001:2015, ISO 14001:2015, & ISO 45001:2018
Internal Auditor: AS9100D (Aerospace), IATF 16949:2016 (Automotive), ISO/IEC 17001, ISO 13485:2016, ISO 9001:2015, ISO 14001:2015, & ISO 45001:2018
Overview:
These specialized courses are designed to equip participants with the necessary skills to conduct effective internal audits tailored to each respective standard. Participants will gain an in-depth understanding of auditing practices as outlined in ISO 19011, including key phases such as planning, execution, reporting, and follow-up. Each course focuses on a specific standard to ensure detailed and targeted knowledge of the relevant quality, environmental, safety, or industry-specific management system.
Course Options:
- AS9100D (Aerospace) – Focuses on aerospace industry quality management, including risk management, product safety, and counterfeit part prevention.
- IATF 16949:2016 (Automotive) – Concentrates on automotive industry quality management, with an emphasis on defect prevention, risk management, and continuous improvement.
- ISO/IEC 17001 – Concentrates on the requirements for conformity assessment and impartiality management.
- ISO 13485:2016 (Medical) – Dedicated to medical device quality management systems with an emphasis on regulatory requirements.
- ISO 9001:2015 (General) – Quality management principles across various industries, ensuring continual improvement and customer satisfaction.
- ISO 14001:2015 (Environmental) – Focuses on environmental management systems, addressing waste reduction and sustainability.
- ISO 45001:2018 (Occupational Health & Safety) – Dedicated to health and safety management, aimed at reducing workplace risks and improving worker safety.
Key Benefits:
- Tailored learning for each individual standard
- Gain practical knowledge of compliance for each standard
- Develop skills in planning, conducting, and reporting on internal audits specific to the chosen standard
- Understand the requirements external auditors will assess for ISO certification
Course Objectives:
- Learn to effectively audit for compliance with your chosen standard
- Familiarize yourself with ISO 19011 auditing standards and best practices
- Identify potential non-conformities and areas for improvement within your organization
Duration:
12-16 hours (per course, depending on the standard)
Certification Notes:
Participants will receive a course completion certificate upon successful completion.
Enrollment:
Click the "Send a Request" button below to learn more about the courses and schedule
a consultation with our expert.
1.6.9 Combined ISO 9001:2015, ISO 14001:2015, and ISO 45001:2018 Management Systems
Combined ISO 9001:2015, ISO 14001:2015, and ISO 45001:2018 Management Systems
Overview:
This course is designed to guide companies through the combined implementation of ISO 9001:2015 (Quality Management Systems), ISO 14001:2015 (Environmental Management Systems), and ISO 45001:2018 (Occupational Health and Safety Management Systems). Even without prior knowledge of these standards, organizations can efficiently integrate and align their quality, environmental, and occupational health and safety systems into a unified management framework with hands-on training and implementation assistance.
By merging these standards, companies can streamline compliance efforts, simplify internal processes, and reduce overall third-party registration costs. This course provides essential tools and guidance for businesses aiming for registration within a year.
Key Benefits:
- Integrated Management System (IMS): Learn how to combine quality, environmental, and occupational health and safety systems into one cohesive framework.
- Hands-on Training: Practical guidance and support throughout the entire implementation process.
- Cost Savings: Reduce registration and auditing expenses by implementing a single, integrated system.
- Enhanced Efficiency: Streamline operations, reduce duplication, and ensure continuous improvement across all management areas.
Course Objectives:
- Understand the core requirements of ISO 9001:2015, ISO 14001:2015, and ISO 45001:2018
- Learn how to develop and implement an integrated management system (IMS)
- Identify synergies between the three standards to optimize processes and reduce redundancies
- Prepare your organization for third-party audits and certification
Duration:
16 hours
Certification Notes:
Participants will receive a course completion certificate upon successful completion.
Enrollment:
Click the "Send a Request" button below to learn more about the courses and schedule
a consultation with our expert.
1.6.10 Food Safety – HACCP
Food Safety – HACCP
Overview:
The Basic HACCP workshop is an intensive two-day course (16 hours) focused on the philosophy and principles of the Hazard Analysis and Critical Control Point (HACCP) System. This course will equip participants with the knowledge and skills necessary to implement HACCP effectively within their organization. The training curriculum is based on the guidance provided in the March 20, 1992 National Advisory Committee on Microbiological Criteria for Foods HACCP document, along with subsequent revisions and aligns with the intent and requirements of the USDA, FSIS HACCP regulation.
Throughout the workshop, participants will engage in practical exercises and discussions that will enable them to develop up to 30% of their HACCP plan during class.
Key Benefits:
- Comprehensive Understanding: Gain insight into the core principles of the HACCP system and its importance in food safety management.
- Hands-On Experience: Participate in practical exercises to develop a HACCP plan relevant to your organization.
- Regulatory Compliance: Understand how HACCP aligns with USDA and FSIS regulations to ensure your organization meets food safety standards.
- Specialized Classes: Opportunities to further enhance your knowledge through Advanced HACCP and Recall Management workshops.
Course Objectives:
- Understand the principles and philosophy of the HACCP system
- Learn the steps necessary to conduct a thorough hazard analysis
- Develop critical control points and monitoring procedures
- Gain skills to create and implement an effective HACCP plan
Duration:
16 hours (2 days)
Certification Notes:
Participants will receive a course completion certificate upon successful completion.
Enrollment:
Click the "Send a Request" button below to learn more about the courses and schedule
a consultation with our expert.