Get documents about "Statistics for Quality Control and Process Validation: Comparing Multiple Sets of Data
W
Description
This webinar will serve as an introduction to the Design of Experiments (DOE) by expanding upon the concept of the Analysis of Variance (ANOVA) that was presented in an earlier webinar. The webinar will describe the concepts of blocking and randomization to remove sources of variability, and present an analysis of a design containing a single block with multiple subjects. The webinar will contain a brief review of the earlier presentation on ANOVA. Studies will be based data generated in a pharmaceutical company.
Document Sample
Toll Free Number: 800-447-9407
Live Webinar on
Statistics for Quality Control and Process Validation: Comparing Multiple
Sets of Data
Date: Thursday, March 14, 2013 Time: 10:00 AM PST | 01:00 PM EST
Course "Statistics for Quality Control and Process
Validation: Comparing Multiple Sets of Data " has Duration: 90 Minutes
been pre-approved by RAPS as eligible for up to 1.5 Instructor: Steven S Kuwahara
credits towards a participant's RAC recertification Location: Online
upon full completion.
Steven S Kuwahara
Founder & Principal, GXP Register Now
Biotechnology, LLC
Steven S. Kuwahara, Ph.D. is the founder and Principal of GXP BioTechnology LLC, a consulting firm that
works in the areas covered by the GLP and GMP of drugs, biologics, and nutraceuticals. Steve has over 30
years of experience in supervising quality control laboratories, ...more
Overview:
This webinar will serve as an introduction to the Design of Experiments (DOE) by expanding upon
the concept of the Analysis of Variance (ANOVA) that was presented in an earlier webinar.
The webinar will describe the concepts of blocking and randomization to remove sources of
variability, and present an analysis of a design containing a single block with multiple subjects. The
webinar will contain a brief review of the earlier presentation on ANOVA. Studies will be based data
generated in a pharmaceutical company.
Areas covered in the session:
l A review of the basic ANOVA method and the
equations used for generating F-values and the
corresponding p values.
l The concept of blocking.
l Analysis of an unblocked experiment
l Analysis of the same experiment after blocking
Who Will Benefit:
l Regulatory Affairs
personnel who prepare
the CMC sections of Suggest a Topic
submissions.
l Development personnel More Webinars
who will set the early
specifications.
l R & D personnel who will
contribute data for use in
development. Click here to
l Project managers for register for this
product development webinar
studies.
l Quality systems auditors
l Consultants.
It would be really nice if you can circulate this mail to all your deserving colleagues who can
immensely benefit from this program.
For more information, please contact the event coordinator. We look forward to seeing you at the webinar.
Best regards,
Event-coordinator
GlobalCompliancePanel
About GlobalCompliancePanel
GlobalCompliancePanel is an online knowledge fulfillment community portal & it has put together a new model
for online compliance training by creating a single window of learning opportunities for compliance
professionals & providing a forum for expert speakers/panelists to render their services through simplified
online training delivery mechanisms. Our commitment is give compliance regulatory training, showcasing of
best industry practices & quality enrichment training sessions in a most cost effective manner. Compliance
professionals can benefit from a wide range of training sessions, giving a diverse choice of events & all
sessions being either Live or recorded stream or in the form of audio CDs. GlobalCompliancePanel portal
ensures a secure & cost effective online environment and also support your E-learning and development
on/through our website. Keep track of all webinars arranged for your industry through notifications & event
calendars being mailed to your inbox. GlobalCompliancePanel opens new doors of learning opportunities for
professionals.
GlobalCompliancePanel
www.globalcompliancepanel.com
43337 Livermore Common, Fremont,
CA 94539, USA
Phone: 800-447-9407 or
Fax your PO to: 302-288-6884
If you do not wish to receive this training alerts from GlobalCompliancePanel Click Unsubscribe
Other docs by globalcompliancepane
Maintaining a Validated State - PV, PM and Statistics associated with Current Regulations
Views: 8 | Downloads: 0
2-day In-person Seminar on " Mastering the HIPAA Privacy, Security, and Breach Notification Rules: Coping with Rule Changes, Managing Incidents, Preparing for Audits, and Avoiding"
Views: 157 | Downloads: 0
FDA 510(k): Preparation, Submission, and Clearance - Webinar By GlobalCompliancePanel
Views: 9 | Downloads: 0
