Description
This webinar will provide valuable assistance to all FDA and EMEA regulated companies that need to validate their cleaning and disinfection programs.

The basics of personnel practices and cleaning and disinfection will be discussed. The most common source of contamination in the cleanroom is people and as such it is important to cover common mistakes in behavior and gowning. Facility design and conditions will be addressed as well since these are also a contributor to contamination. The end user will get a complete overview the basics of how to control their cleanroom environment how to get he best possible yield of products.

Areas Covered in the seminar: * Review the most common mistakes people make in cleanrooms that lead to contamination. * Learn how to develop a successful contamination control program. * Learn ways to improve facility design and maintenance. Who will benefit: This webinar will provide valuable assistance to all FDA and EMEA regulated companies that need to validate their cleaning and disinfection programs, including companies in the Pharmaceutical, Biotech, and Medical Device fields. The employees who will benefit include: * QA and QC Managers * Disinfectant Validation Managers * Operations Managers * Cleanroom Managers * Personnel and contractors that clean and disinfect cleanrooms * Regulatory Compliance Managers & Environmental Monitoring Managers