The Cutting Edge of Medical Technology Content, Community & Collaboration
Time: September 28, 2017 at 9am to September 29, 2017 at 6pm
Location: DoubleTree by Hilton Las Vegas Airport
Street: 7250 Pollock Drive Las Vegas, NV USA 89119
City/Town: Las Vegas, NV
Website or Map: http://www.globalcompliancepa…
Event Type: online, healthcare, training, courses
Organized By: NetZealous DBA as GlobalCompliancePanel
Latest Activity: Jul 25, 2017
Course "Design of Experiments (DOE) for Process Development and Validation" has been pre-approved by RAPS as eligible for up to 12 credits towards a participant's RAC recertification upon full completion.
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.
The use of DOE methodology provides a means to identify process parameters which impact product quality (critical process parameters) and determine the functional relationship that links the process parameters to those critical quality attributes. Screening designs, such as 2k factorial and D-optimal designs, are used to determine critical process parameters. Response surface designs, such as Central Composite Designs (CCDs) and I-optimal designs, are used to model the functional relationship between those critical process parameters and the critical quality attributes.
Location: Las Vegas, NV Date: September 28th & 29th, 2017 and Time: 9:00 AM to 6:00 PM
Venue: DoubleTree by Hilton Las Vegas Airport 7250 Pollock Drive Las Vegas, NV USA 89119
Register now and save $200. (Early Bird)
Price: $1,295.00 (Seminar Fee for One Delegate)
Until August 20, Early Bird Price: $1,295.00 From August 21 to September 26, Regular Price: $1,495.00
Register for 5 attendees Price: $3,885.00
$6,475.00 You Save: $2,590.00 (40%)*
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