This training will benefit those involved in the manufacturing, processing, testing and release of sterile and non-sterile products. It will provide the attendee an understanding of the basic concept of microbiology, microbiological and contamination control practices, cleanroom design, routine testing, qualification/validation and use of cleanrooms as well as the typical sterilization processes (Physical and Chemical) within various industries such as the Pharmaceutical, Biotechnology, Drug, Biologics, Medical Device and In-vitro Diagnostics Product Manufacturing Industries, especially personnel and management in:
- Quality Assurance
- Quality Control
- Manufacturing
- Validation
- Supplier Quality Assurance
- Regulatory Affairs
- Shipping and Receiving
- Facility and Maintenance
- Engineering
- Materials Management
- Analysts
- Analytical Chemists
- All levels of management
- Microbiologist
By Kelly Thomas