Best Practices for an Effective Cleaning Validation Program
15-Hour Live Stream or On-Site
2025 Course Dates will be available soon. Please join the wait list or request on-site delivery details.
Course Director
Course Fee
$2150.00 Regular Registration
$1950.00 Early Bird Pricing (Register 30 Days in Advance)
Course Brochure
Future Live Stream Sessions (click to register)
Cleaning Validation Best Practices Course Description
This course provides practical guidance on cleaning validation regulatory compliance, in conjunction with process validation principles to facilitate reasonable and informed decision making and activity planning. Regulatory requirements and the latest industry practices will be included in the discussion to identify questionable practices that may be misdirected as well as the better practices that support and align with current process validation principles. The program will describe a risk-based approach for establishing an effective cleaning validation program, including the development of policies, master plans and the appropriate content for each study to be performed incorporating critical quality attributes and critical process parameters and process control. In addition, validation maintenance and life cycle aspects will be reviewed. Cleaning validation examples will be included from different sterile and non-sterile product types, and different types of dosage forms including oral, topical, and injections. Concepts will apply to any FDA regulated manufacturing including drugs, supplements, personal care, medical devices. Additional benefits of this class include interacting and learning from peers. Participants will have the opportunity to discuss their challenges and problems.
Additional benefits of this class include interacting and learning from peers. Participants will have the opportunity to discuss their challenges and problems.
Who Should Attend
Attendance at this 15 hour course will be beneficial to personnel directly involved or supporting the development of cleaning validation programs and plans, also those responsible for cleaning validation protocols and execution activities, as well as beginning or experienced personnel who may eventually participate in such efforts. This includes:
- Validation,
- Engineering,
- Operations, and laboratory personnel,
- Analytical Method Development,
- Quality Control and Quality Assurance personnel.
Individuals in management who interact internally with these teams or externally with regulatory agencies will also benefit from attending this course. There are no prerequisites for attending, but a basic knowledge of general science and process validation is helpful.
Related Courses
- Aseptic Processing in the Manufacture of Biotech and Pharmaceutical Products™
- Cleanroom Fundamentals: Regulation, Science, Design, Practice, Operation & Management
- Process Validation for Drugs and Biologics
- Medical Device Process Validation Training for Professionals
- Good Laboratory Practices (GLP) for Nonclinical Laboratory Studies
- Good Manufacturing Practices (cGMP)
Registrant Information:
Each person attending a course will be asked to set up an Attendee Profile Account during the registration process. Creating an Account helps you view your order history and manage your training programs. If you are registering for others, please set up an Account in the Attendee’s name. If you are registering more than one person, you’ll need to set up a separate account for each Attendee.