This Webinar will explain how to write a Cleaning Validation Master Plan. This webinar will discuss that what are the critical elements have to be considered when designing a cleaning validation program at a Pharma plant.
This one-hour seminar is designed to discuss the principles applied to the cleaning validation in a pharmaceutical industry. It will explain how to write a Cleaning Validation Master Plan and what are the critical elements have to be considered when designing a cleaning validation program at a Pharma plant.
This one-hour seminar is designed to discuss the principles applied to the cleaning validation in a pharmaceutical industry. It will explain how to write a Cleaning Validation Master Plan and what are the critical elements have to be considered when designing a cleaning validation program at a Pharma plant.
Areas Covered in the seminar:
- Regulatory Aspects.
- Selection of worst case product or products.
- Levels of Cleaning, Cleaning Parameters, Type of Cleaning.
- MVP.
- Calculation of chemical residue limits based on.
- Therapeutic Dose.
- Toxicity Dose.
- Calculation for Equipment train.
- Microbiological aspects of cleaning and Calculation of limits Revalidation.
Who Will Benefit:
Those who are working in pharmaceutical manufacturing facilities and are responsible and involved in the activities, such as the equipment cleaning, maintenance and monitoring on an ongoing basis.- Validation Staff
- Manufacturing Operators
- Microbiologist
- Production Management
- Staff directly involved in compounding and filling operation
- QA Staff
- Team Members of Quality Management System (QMS)
- Contractors
- Consultants
Course Provider
Nazia Dar,
