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

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GlobalCompliancePanel, a leading regulatory and compliance training gateway, will host a two-day, in-person seminar on the topic, “Design of Experiments and Statistical Process Control for Process Development and Validation” on February 7 and 8 at Orange County, CA.

Orange City, CA, USA., Feb 7, 2013 - (PressReleasePoint) -

Course Agenda:
The soul of this this course is a presentation of the procedures that 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.
How to go about doing this work requires a practical orientation. It calls for an approach with case studies and examples. This seminar will fulfill this requirement. It 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.
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Purpose of the seminar
Any pharmaceutical worker, who performs, supervises or reviews manufacturing or testing processes needs to understand the relationships among the process parameters. This knowledge should enable the worker to monitor the performance of processes and test methods.
This is particularly true for the worker in Quality Control and Quality Assurance, especially in the backdrop of the recent FDA guidance document on Process Validation that has assigned the responsibility for reviewing and interpreting DOE and SPC studies to the Quality Unit.
The actual work, however, is done by the development, manufacturing, or quality systems worker. This session will help such workersget a hands-on experience of how to design the systems and studies and interpret the results generated. It will offer them valuable assistance in how to actually get about their work of designing studies and systems. As a result of this learning, participants will be able to work on these aspects in accordance with FDA requirements.
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DATE AND VENUE:
February 7 and 8, 2013
Seminar Timings: 9am to 6pm EST
Venue:Will be announced soon
Price –$ 1495;
Group discounts available in the following pattern:
Send two attendees: Get a discount of 10%
Send three to six attendees: Get a discount of 20%
Send seven to 10 attendees: Get a discount of 25%
Send 10 attendees or more: Get a discount of 30%
To avail the above group discounts, all the participants should register by making a single payment.Please contact Customer Care at 1800 447 9407
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Contact Information:
Event Coordinator
Toll free: 1800 447 9407
Fax: 302 288 6884
Email: support@globalcompliancepanel.com
Website:https://www.globalcompliancepanel.com/
GlobalCompliancePanel
NetZealous
USA Livermore Common, Fremont,
CA 94539, USA
Phone: 1800 425 9407