STERIS Master Class: Applied Cleaning Validation Practices
Overview
This 2-day immersive training experience led by invited industry experts will explore current practices, regulatory expectations and emerging trends in cleaning and cleaning validation. This course is designed specifically for biopharmaceutical manufacturers aiming to build or maintain a high-quality, efficient, and compliant cleaning process. Through a mix of expert instruction, real-world case studies, and hands-on exercises using cutting-edge bioprocessing equipment at the NIBRT facility, participants will tackle current challenges and gain practical skills that can be immediately applied in their operations.
Key topics covered
- End-to-end lifecycle approach to cleaning validation
- Cleaning chemistries and their applications in process equipment
- CIP, COP and manual cleaning methods
- Process design and qualification
- Setting acceptance criteria
- Establishing and validating analytical methods
- Rinse and surface sampling techniques
- Riboflavin coverage testing and visual inspection
- Protocol development and grouping strategies
- Stainless steel preservation
- Managing bioburden and biofilms
- Navigating Annex 1 compliance
Who should attend
This course is ideal for professionals looking to build or enhance their foundational knowledge of cleaning and cleaning validation including:
Quality Assurance * Regulatory * Quality Control * Validation * Operations * Microbiology * Facilities Maintenance * Engineering * Plant Management
What do Attendees Obtain on Completion?
Attendees will receive a certificate of completion.
Register
Course Format
Onsite at NIBRT
2 full days onsite training at NIBRT facility
Dates & Price
Dates:
- Course 1 15/04/2026 - 16/04/2026€2,150.00
15 Places Remaining
