Description
A strong Quality System is the backbone of every successful pharmaceutical and industrial operation.
This Quality Systems Course provides a deep, practical understanding of how to design, implement, control, and continuously improve a robust Quality Management System (QMS) aligned with GMP, ISO, and regulatory expectations.
Participants will learn how quality systems integrate across all departments, ensuring compliance, efficiency, and consistent product quality.
The course offers a structured walkthrough of essential QMS elements, including documentation control, change management, deviations, CAPA, internal audits, supplier qualification, quality risk management, product quality review, data integrity, and ongoing lifecycle management.
Through case studies, templates, and real-world examples from the pharmaceutical, food, and chemical industries, trainees gain the skills needed to confidently manage and evaluate a full QMS.
By the end of this course, participants will be able to:
- Understand the structure and principles of an effective Quality Management System.
- Apply GMP and ISO-based quality requirements across operations.
- Control documents, records, and change systems properly.
- Investigate deviations, implement CAPA, and conduct internal audits.
- Build risk-based processes and ensure continual improvement.
- Strengthen inspection readiness for regulatory bodies.
Who Should Attend
This course is ideal for professionals who work with or oversee quality systems, including:
- Quality Assurance (QA) Specialists & Managers
- Quality Control (QC) Personnel
- Production & Operations Supervisors
- Validation & Engineering Teams
- Regulatory Affairs Professionals
- New Graduates seeking QA/QC careers
- Anyone responsible for maintaining or improving a QMS in a regulated environment
Key Takeaways
- Flexible Attendance Options – Join in-person at VALOR or virtually through our live interactive platform.
- Recorded Sessions – Enjoy limited access to recordings for one month after course completion for review and reinforcement.
- Repeat for Free – Participants may re-attend inperson any future round of the same course at no additional cost.
- Accredited Certificate – Receive a QR-coded certificate for authenticity verification and professional recognition.
- Comprehensive Resources – Access digital materials, trainer support, and post-course assessments through VALOR’s e-learning platform.
Course Topics
- Quality management system(QMS)
- Audits and self-inspections and CAPA
- Risk management
- Documentation
- Data Integrity and Data Governance
- Change control and Deviation management, complaints, and adverse event Reports
- Product trend requirements PQR
- Supplier and contractor quality management.
Number Of Sessions
8 Sessions