STERIS Master Class: Applied Cleaning Validation Practices

Overview

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

  • Lifecycle approach to cleaning validation
  • Cleaning chemistries and applications for process equipment
  • CIP, COP and manual cleaning methods
  • Process design and qualification
  • Setting acceptance criteria
  • Analytical methods and validation
  • Rinse and surface sampling techniques
  • Riboflavin coverage test and visual inspection
  • Protocols and grouping strategies
  • Stainless steel maintenance
  • Bioburden and biofilms
  • Global regulatory documents

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. 

Register

STERIS Master Class: Applied Cleaning Validation Practices

1,990.00

STERIS Screenshot

Course Format

Onsite at NIBRT

2 full days onsite training at NIBRT facility 

 

Dates & Price

Dates:
  • Course 1
    30/04/2025 - 01/05/2025

    2 Days Onsite at NIBRT

    1,990.00

    16 Places Remaining

  • Course 2
    08/10/2025 - 09/10/2025

    2 Days Onsite at NIBRT

    1,990.00

    16 Places Remaining

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