STERIS Master Class: Applied Cleaning Validation Practices


This 2-day intensive course presented by invited industry experts will cover industry practices and regulatory expectations and trends in cleaning and cleaning validationIt is designed for biopharmaceutical manufacturers who are concerned about developing or maintaining a high-quality, efficient, and most importantly, compliant cleaning process. The training will address several current challenges to cleaning and validation in the biopharmaceutical industry, and include case studies, best practices, and hands on exercises using state-of-the-art bioprocessing equipment located in the NIBRT facility.  

Key topics covered

  • An overview of the life cycle approach to cleaning validation, process design and qualification, protocols and grouping strategies, dedicated equipment and campaigns and how to set acceptance criteria. 
  • Example of global regulatory documents and citations.

Who should attend

This course is suitable for personnel from Quality Assurance, Regulatory, Quality Control, Validation, Operations, Microbiology, Facilities Maintenance, Engineering, Plant Management disciplines. 

What do Attendees Obtain on Completion?

Attendees will receive a certificate of completion. 


STERIS Master Class: Applied Cleaning Validation Practices


STERIS Screenshot

Course Format

Onsite at NIBRT

2 full days onsite training at NIBRT facility 


Dates & Price

  • Course 1
    15/10/2024 - 16/10/2024

    2 Days Onsite at NIBRT


    16 Places Remaining

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