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Cleaning Validation Seminars for Pharmaceutical Manufacturers
Cleaning and Cleaning Validation is a two-day pharmaceutical cleaning validation class for pharmaceutical manufacturers addressing the practical aspects of meeting FDA cleaning validation process requirements.
The class focuses on cleaning and cleaning validation of product contact surfaces in process manufacturing; please note that it does not cover general environmental cleaning in cleanrooms.
- Cleaning Objectives
- Validation Programs
- FDA Expectations
- Cleaning Technologies
- Process and Engineering Issues
- Cycle Development
- Residues and Limits for Cleaning Agents
- Microbial Issues in Process Manufacturing
- Issues in Non-Routine Cleaning Analysis and Sampling
- Cleaning SOPs
- Validation Protocols
- Monitoring Issues
- Trouble Shooting
- Cleaning Problems
Fee: $ 5,000 USD plus Travel Expenses for Speakers (includes seminar and seminar notes for up to 50 attendees.
To inquire about scheduling a seminar at your site: Call 314.290.4743 or contact your STERIS account manager
Presenters: The presenters for this seminar are Destin LeBlanc, Principal Partner, Cleaning Validation Technologies LLC, in San Antonio, Texas, and George Verghese, Manager of Pharmaceutical and Research Technical Services in St. Louis, Missouri.