Disinfection and Clean room Cleaning in a FDA Regulated Environment
Overview:
This live webinar concentrates on proper cleanroom cleaning, and discusses tools, equipment, agents, personnel training, extent, and frequencies. It is a very practical training session intended to assist personnel involved in the design, cleaning, monitoring, and assessment of cleanroom cleaning procedures. The key benefits of this course are:
- In-depth understanding of cleanroom cleaning methods.
- Achieve satisfactory inspections more easily.
- Higher assurance of new medical product approvals.
- Minimize non-conformances.
- Reduce rates of batch rework and rejections.
- Reduce cleaning-related environmental contamination issues.
- Avoid product recalls.
- Understand industry standards in cleanroom cleaning
Why should you attend: Cleanroom cleaning processes and methods have been scrutinized by FDA auditors due to their important role in cleanroom management. Poor or substandard cleaning can result in manufacturing delays, non-conformances, recalls, and regulatory action. Therefore it is important to control cleanroom cleaning processes and ensure best practices are followed.
Areas Covered in the Session:
- Learn about cleaning and what it accomplishes in the cleanroom.
- Identify cleaning agents, tools, and equipment.
- Discuss cleaning personnel training and qualification.
- Identify the methods of cleanroom cleaning.
- Identify and discuss extent and frequency of cleanroom cleaning.
Who Will Benefit:
- Q auditors and personnel
- Manufacturing Operators
- Maintenance Cleaning Personnel
- Consultants
- Operations managers
- Microbiologists
- Validation Personnel
- Training departments