
About the Course
🧩 Course Outline:
Module 1: Introduction to ISO 9001 Documentation
Purpose of documentation in a QMS
Key definitions: documented information, records, procedures
Overview of ISO 9001:2015 Clause 7.5
Module 2: Types of ISO 9001 Documentation
Quality Policy and Objectives
Quality Manual (optional but beneficial)
Process maps and procedures
Work instructions and SOPs
Records and forms
Module 3: Document Control (Clause 7.5.3)
Document identification and approval
Version control and change management
Access and distribution
Retention and disposal
Module 4: Building a Documented QMS
Mapping processes to clauses
Writing clear, user-friendly documents
Templates and formatting standards
Real-life examples and sample templates
Module 5: Internal Auditing of Documentation
Evaluating compliance through audits
Common nonconformities related to documentation
Tips for continuous improvement
Module 6: Workshop / Case Study
Analyze a sample company's documentation system
Identify gaps and recommend improvements
At the end of the course, participants will receive a non-accredited certificate of participation.
Course language : English
Join us from anywhere — this course is offered as an interactive online workshop.
🧾 Target Audience:
- Quality Managers and Officers
- Internal Auditors
- ISO 9001 Implementation Teams
- Any professional involved in QMS documentation
Your Instructor
Our instructors are certified Six Sigma professionals with extensive experience in quality management, process improvement, and data analysis. They have led numerous industry-focused training sessions in Six Sigma, Lean Manufacturing, and advanced problem-solving methodologies across Germany and internationally. With a strong background in both academic research and industrial practice, the instructor brings real-world insights to every training session, empowering participants with practical tools and strategies for quality excellence. At the end of the course, participants will receive a non-accredited certificate of participation.
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