Manual Visual Inspection Essentials: Navigating Regulations, Identifying Defects, and Analysing Root Causes
Overview
This course introduces the core principles and practices of manual visual inspection (MVI) in biopharmaceutical manufacturing. Participants will explore regulatory expectations, learn to identify common defect types, and gain insight into root cause analysis techniques. The course balances foundational knowledge with practical considerations, supporting quality and compliance in sterile product inspection.
Key topics covered
- Explore the role of manual visual inspection in ensuring product quality and patient safety.
- Outline regulatory requirements and industry standards for MVI.
- Recognize common defect types and their potential impact on product integrity.
- Discuss factors influencing inspection performance, including human, environmental, and equipment variables.
- Deepen your understanding of defect root cause by troubleshooting practical manufacturing scenarios
Who should attend
This course is suitable for operators, quality professionals, and technical staff involved in visual inspection of sterile products. It is also relevant for those in manufacturing, QA, or training roles who support inspection activities or investigate defect-related issues.
What do Attendees Obtain on Completion?
An MCQ quiz will be taken at the end of the course. Attendees will receive results and a certificate of completion.
Register
Course Format
Onsite Training at NIBRT
- 2 full days onsite training at NIBRT facility
Dates & Price
Dates:
- Course 1 15/04/2026 - 16/04/2026€2,150.00
8 Places Remaining
