Charisma

#	Content
1	Module 1: Introduction to Cleaning, Sanitization, and
2	Module 2: Fundamentals of Cleaning
3	Module 3: Sanitization and Disinfection
4	Module 4: Sterilization Methods
5	Module 5: Cleaning Validation
6	Module 6: Sterilization Validation
7	Module 7: Environmental Monitoring and Contamination Control
8	Module 8: Equipment and Facility Cleaning
9	Module 9: Documentation and Record Management
10	Module 10: Regulatory Compliance and Continuous Improvement

#	Outcomes
	• Explain the role of cleaning, sanitization, and sterilization in pharmaceutical Quality Management Systems.
	• Select suitable cleaning and sterilization methods based on equipment, products, and contamination risks.
	• Develop and implement Standard Operating Procedures (SOPs) for cleaning and sanitization.
	• Perform cleaning validation and interpret validation results.
	• Apply disinfectant rotation and sanitization programs effectively.
	• Monitor environmental cleanliness using microbiological and particulate monitoring techniques.
	• Identify contamination risks and implement preventive controls.
	• Maintain compliant documentation and records.
	• Support GMP inspections and regulatory audits related to cleaning and contamination control.
	• Contribute to continuous improvement of contamination control programs.

#	Participants
1	� • Quality Assurance (QA) professionals
2	� • Quality Control (QC) analysts and microbiologists
3	� • Production managers and supervisors
4	� • Manufacturing operators
5	� • Validation engineers
6	� • Microbiology laboratory personnel
7	� • Engineering and maintenance personnel
8	� • Cleanroom and environmental monitoring staff
9	� • Warehouse personnel
10	� • Regulatory Affairs professionals
11	� • GMP auditors
12	� • Pharmaceutical, biotechnology, medical device, cosmetic, and food manufacturing professionals