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Design of Experiments and Statistical Process Control for Process Development and Validation

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					                                                                                       Phone: 800-447-9407
                                                                            support@globalcompliancepanel.com


2-day In-person Seminar on

Design of Experiments and
Statistical Process Control for
Process Development and Validation
Location: Orange County CA | February 7th & 8th, 2013 | 9 AM to 6 PM EST
                                                                                         Register Now
Location: Philadelphia, PA | May 23rd & 24th, 2013 | 9 AM to 6 PM EST

                                                   Course "Design of Experiments and Statistical
By Dr. Steven S Kuwahara                           Process Control for Process Development and
Price: $1,295.00 (for 1 attendee)                  Validation" has been pre-approved by RAPS as eligible
Register now and save $200. (Early Bird)           for up to 12 credits towards a participant's RAC
                                                   recertification upon full completion.


Course Outline: Day 1:                                                                        Dr. Steven S
                                                                                              Kuwahara
Lecture 1: Introduction                                                                       Founder &
Lecture 2: One Level, One Factor Designs. Simple Comparisons.                                 Principal, GXP
                                                                                              Biotechnology,
Lecture 3: Two-Level Multi-factorial Design                                                   LLC
Lecture 4: Extracting Information from the Experiment

                                                                             Dr. Steven S. Kuwahara Ph.D. is
                                                                             the founder and Principal of GXP
                                                                             BioTechnology LLC, a consulting
                                                                             firm that works in the areas
Course Outline: Day 2:
                                                                             covered by the GLP and GMP of
                                                                             drugs, biologics, and
Lecture 5: Shewhart Charts for Variable Data                                 nutraceuticals.
Lecture 6: Shewhart Charts for Attribute Data Especially Counts.             Steve has over 30 years of
                                                                             experience in supervising quality
Lecture 7: Considerations from Shewhart Charts
                                                                             control laboratories, including an
Lecture 8: Other Types of Charts Related to Shewhart Charts                  animal testing facility, and in
                                                                             performing GLP and GMP audits of
                                                                             internal and external testing
                                                                             laboratories.

Overview:

This course will present the procedures that must be used in the application of DOE and SPC to the
development, design and monitoring of manufacturing and testing processes. A practical approach
with case studies and examples will be used, with theoretical information introduced only when
necessary to understand an experiment. Examples from real processes and testing procedures will
be used to present the student with examples that will be directly applicable to their work.

Who Will Benefit:

    l   Directors                                               
    l   Managers
    l
    l
        Supervisors
        Lead workers in Process Development
                                                                               venue
                                                                        WILL BE ANNOUNCED SOON
    l   Manufacturing
    l   Regulatory Affairs
    l   Quality Assurance and Quality Control                                Register Now
    l   Workers who will be participating in operations
        or the supervision of the development,                  
        manufacturing, or testing of medicinal products
        will benefit from knowing the procedures and
        applications of DOE and SPC.


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
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GlobalCompliancePanel
www.globalcompliancepanel.com
Livermore Common, Fremont,
CA 94539, USA


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DOCUMENT INFO
Description: This course will present the procedures that must be used in the application of DOE and SPC to the development, design and monitoring of manufacturing and testing processes. A practical approach with case studies and examples will be used, with theoretical information introduced only when necessary to understand an experiment. Examples from real processes and testing procedures will be used to present the student with examples that will be directly applicable to their work.