Location: Raleigh, NC

Applied Cleaning Validation Practices: A STERIS Master Class
July 30 - 31, 2019

This 2-day intensive course presented by invited industry experts will cover industry practices and regulatory expectations and trends in cleaning and cleaning validation.  It 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 BTEC facility.

Topics Including:
1. Lifecycle approach to cleaning validation
2. Cleaning chemistries & application parameters
3. Laboratory studies and scale up
4. CIP, COP, Manual cleaning methods
5. Process and engineering Issues
6. Cleaning process equipment-bioreactors, rings, membranes
7. Cycle development
8. Process design and qualification

Who Should Attend? 
Scientists and engineers working in the Biomanufacturing industry including roles such as Quality Assurance, Regulatory, Quality Control, Validation, Operations, Microbiology, Facilities Maintenance, Engineering, and Plant Management disciplines.

Attend and you will receive:
Notebook containing all course lecture and lab materials
Morning break
Afternoon break
Certificate of attendance

Fee:  $1,350

Click Here to Register