Prior to developing a process control plan as part of an overall risk management strategy, process development studies must be completed. The objective of these process development studies is to gain knowledge and understanding about how variation in process parameters explains variation in the product quality characteristics of the product.
Why should you attend?
The Global Harmonization Task Force (GHTF) Process Validation Guidance for Medical Device Manufacturers provides guidance on where design of experiments should be applied during process validation; it suggests the use of both screening and response surface designs during Operational Qualification.
Areas Covered in the Session:
Learn how to effectively use JMP to:
• identify critical quality attributes (CQAs) that will be used as responses in your designs
• utilize risk management tools to identify and prioritize potential critical process parameters
• identify critical process parameters and develop a functional relationship between those process parameters and your critical-to-quality attributes (CQAs) using both screening and response surface designs
Location: Los Angeles, CA Date: March 30th & 31st, 2017 and Time: 9:00 AM to 6:00 PM
Venue: Four Points by Sheraton Los Angeles International Airport
Address: 9750 Airport Boulevard, Los Angeles, CA, 90045, United States
Use CNY2017 Promo Code to Get Flat 50% OFF on ALL SEMINARS
Expire Date : 01-January-2017
Price: $1,295.00 (Seminar Fee for One Delegate)
Until February 20, Early Bird Price: $1,295.00 from February 21 to March 28, Regular Price: $1,495.00
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