Getting Design of Experiments and Statistical Process Control right for Process Development and Validation
Procedures must be used in the application of DOE and SPC to the
development, design and monitoring of manufacturing and testing processes. Why
this needs to be done is because the FDA has, in a recent guidance document on Process
Validation, assigned the responsibility for reviewing and interpreting DOE and
SPC studies to the Quality Unit.
Going about doing this work requires a practical orientation. It
calls for an approach with case studies and examples. A seminar that is being
organized by GlobalCompliancePanel, a leading provider of professional
trainings for the regulatory compliance areas, will provide just this and
fulfill this requirement.
Dr.
Steven Kuwahara, Founder and Principal, GXP BioTechnology LLC, will be the Director
at this two-day session. To enroll for this valuable session, please register
by logging on to http://www.globalcompliancepanel.com/control/globalseminars/~product_id=900701SEMINAR. This seminar has been pre-approved by RAPS as
eligible for up to 12 credits towards a participant's RAC recertification upon
full completion.
An
interactive session
Dr. Kuwahara will offer theoretical information introduced only
when necessary to understand an experiment. A highly interactive and practical
session; this seminar offers examples from real processes and testing procedures
and present the participants with examples that will be directly applicable to
their work.
For any pharmaceutical worker who performs, supervises or reviews
manufacturing or testing processes, an understanding of the relationships among
the process parameters and the ability to monitor the performance of processes
and test methods are necessary. This is all the truer of the worker in Quality
Control and Quality Assurance in view of the recent FDA guidance document on Process
Validation.
This work, however, is done by the development, manufacturing, or
quality systems worker. So, synchrony between these two levels of employees is
needed. This course will equip these two levels of employees with the knowledge
of how to design the systems and studies, and interpret the results generated.
Labels: Compliance Training Online, FDA Compliance Training, Online Regulatory Compliance Training, Regulatory Compliance Training
0 Comments:
Post a Comment
Subscribe to Post Comments [Atom]
<< Home