Quality Management and ISO 9000 Regulations Training, Compliance Best Practices and Standards

The Importance of Compliance Training in Quality Management

Quality Management plays an integral role in the growth and performance of your business. It is also key to successful customer relationships. Organizations that maintain quality at all levels provide a superior experience to their customers, employees, and all stakeholders. Quality is maintained by implementing a set of procedures to ensure high performance of products and services and assure that the standards of quality are met.

Whether your organization is part of healthcare, finance, electronics, insurance, or any other industry, quality management has a place. Hence quality management is a training area of interest to most individuals and organizations.

Quality Management Courses, Standards, Best Practices - Topics and Audience

On this page, you will find training programs, and best practice standards useful for a wide range of professionals. Topics covered include product realization processes, administrative processes of a quality management system, and services, failure investigation and root cause analysis, Current Good Manufacturing Practices (cGMP), human error prevention, developing Standard Operating Procedures (SOPs), ISO Standards and more.

Our quality management courses are focused on helping individuals and organizations perform with consistency. Skills imperative to both create and manage quality management systems are taught in our courses. ComplianceOnline connects Quality Management subject matter experts with organizations and professionals looking to learn quality management and compliance to perform their jobs efficiently.

The courses, standards, and best practices on this page are particularly useful for professionals including Quality Managers, Quality Technicians, CEOs, General Managers, Auditors, Management representatives, IT professionals, Professionals in Senior and middle management, Quality Assurance, Regulatory Affairs. R&D, Engineering, Sales and Marketing, Operations / Production, Product development, Training managers and coordinators, regulatory, and compliance officers.

What's Covered

Areas covered in the training programs include U.S. FDA's expectations, FI and RCA's role in a proactive and compliant CGMP System, powerful tools for Root Cause Analysis, Investigation detail, root or probable cause, Investigation detail, root or probable cause, Symptom or problem, Effectiveness, determining and monitoring, Key recent compliance problems and their resolution, Institutionalize vs. "Entropy", General Quality System Requirements, Management Review and Responsibility, Personnel Training, Background on Human Error Phenomena, Human Error and GMP around the world, Importance of Human Error Prevention/reduction, Training and human error, Facts about human error, Human Error as the Root Cause, How is Human Error controlled, Types of error, Human error rates and measurement. Trending and tracking, Prediction, and CAPA effectiveness.