Pharmaceutical Analytical Method Validation and Cleaning Validation

Cleaning is of vital importance to the product safety in the pharmaceutical manufacturing. This training program will cover the key GMP requirements for cleaning validation, the methods of cleaning, effective cleaning procedures, developing effective cleaning procedures, approaches to cleaning validation based on scientific rationale, different analytical techniques, and risk assessment in the cleaning validation. This course provides a detailed and structured introduction to cleaning validation, as well as details of current best practice, cGMP expectations, industry trends and regulatory issues for both the EU and US markets. Therefore, it is suitable for both new and experienced professionals in this field. This course will help the attendees with a better understanding of regulatory requirements and technique.

• State the GMP reasons for cleaning validation
• Interpret regulatory requirements and guidelines
• Outline a strategy for cleaning validation that complies with cGMPs
• Apply risk management principles to identify cleaning validation parameters
• Cleaning process variability & controls
• Develop practical limits for cleaning residues
• Risk based approach to grouping strategy

• Quality assurance
• Quality control
• Validation
• Manufacturing
• Process engineering

Note:
Use coupon code NB5SQH8N and get 10% off on registration.

For Registration:

http://www.complianceonline.com/pharma-cgmp-analytical-method-validation-cleaning-validation-seminar-training-80370SEM-prdsm?channel=sciencedz