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Strategic Partner

October 23, 2017 - October 24, 2017

Applied Statistics for FDA Process Validation

Doubletree by Hilton Houston Intercontinental Airport, Houston, Texas

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Event Details

Begins: October 23, 2017

End: October 24, 2017

Event Location: Doubletree by Hilton Houston Intercontinental Airport, Houston, Texas

Website: http://www.globalc..44SEMINAR

Event Organizer

Event Organizer: Global Compliance Panel

Contact Person:

Phone Number: +1-800-447-9407

Website: https://www.globalcompliancepanel.com/

Overview

In Guidance for Industry Process Validation: General Principle and Practices, process validation is defined as, ""...the collection and evaluation of data, from the process design stage through commercial production.." The guidance further delineates the 'process design stage through commercial production' into three distinct stages of the product lifecycle:

Stage 1: Process Design: The commercial manufacturing process is defined during this stage based on knowledge gained through development and scale-up activities.

Stage 2: Process Qualification: During this stage, the process design is evaluated to determine if the process is capable of reproducible commercial manufacturing.

Stage 3: Continued Process Verification: Ongoing assurance is gained during routine production that the process remains in a state of control.

The first stage of process validation is process design. The Process Validation guidance document states, "A successful validation program depends on information and knowledge from product and process development.

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