MedTech I.Q.

The Cutting Edge of Medical Technology Content, Community & Collaboration

Design of Experiments (DOE) for Process Development and Validation at Singapore

Event Details

Design of Experiments (DOE) for Process Development and Validation at Singapore

Time: July 9, 2015 at 9am to July 10, 2015 at 6pm
Location: Mandarin Orchard Singapore
Street: 333 Orchard Road, Singapore 238867
City/Town: Singapore
Website or Map: https://www.globalcompliancep…
Phone: 18004479407
Event Type: clinical, food, fda, medical, device, defence, and, navy, aerospace, mining
Organized By: GlobalCompliancePanel
Latest Activity: Apr 22, 2015

Export to Outlook or iCal (.ics)

Event Description

Overview:

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 that critical quality attributes. Screening designs, such as 2k factorial and D-optimal designs are used to determine critical process parameters. 

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
  • be able to design and analyze screening designs including a factorial, fractional factorial, and D-optimal design
  • understand the need for adding center points to a design
  • be able to design and analyze response surface designs including central composite designs (CCDs), Box-Behnken designs, and I-optimal designs
  • present results of DOE studies
  • use systematic understanding from DOE studies to update the control plan that is part of the overall risk management plan
Who Will Benefit:
  • Process Scientist/Engineer
  • Design Engineer
  • Product Development Engineer
  • Regulatory/Compliance Professional
  • Design Controls Engineer
  • Six Sigma Green Belt
  • Six Sigma Black Belt
  • Continuous Improvement Manager

Speaker:

Heath Rushing is the cofounder of Adsurgo and author of the book Design and Analysis of Experiments by Douglas Montgomery: A Supplement for using JMP. Previously, he was the JMP and Six Sigma training manager at SAS. He led a team of nine technical professionals designing and delivering applied statistics and quality continuing education courses. 

Location: Singapore Date: July 9th & 10th, 2015        Time: 9:00 AM to 6:00 PM 
Venue:
 Mandarin Orchard Singapore

Venue Address: 333 Orchard Road, Singapore 238867

Price: $2,095.00

(Seminar for One Delegate)

Register now and save $200. (Early Bird)

Contact Information:

NetZealous LLC,

DBA GlobalCompliancePanel

161 Mission Falls Lane,

Suite 216, Fremont, CA 94539, USA         

USA Phone: 800-447-9407

Fax: 302-288-6884

support@globalcompliancepanel.com          

http://www.globalcompliancepanel.com

Registration Link: http://bit.ly/1HJRVWP

 

Comment Wall

Comment

RSVP for Design of Experiments (DOE) for Process Development and Validation at Singapore to add comments!

Join MedTech I.Q.

Attending (1)

© 2024   Created by CC-Conrad Clyburn-MedForeSight.   Powered by

Badges  |  Report an Issue  |  Terms of Service