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Strategic Partner

September 18, 2017 - September 19, 2017

Applied Statistics for FDA Process Validation

The DoubleTree Baltimore-BWI Airport, Baltimore, MD

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Event Details

Begins: September 18, 2017

End: September 19, 2017

Event Location: The DoubleTree Baltimore-BWI Airport, Baltimore, MD

Website: http://www.globalc..42SEMINAR

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. This knowledge and understanding is the basis for establishing an approach to control of a manufacturing process that results in products with desired quality attributes:
Manufactures should:
    Understand the sources of variation
    Detect the presence and degree of variation
    Understand the impact of variation on the process and ultimately on product attributes
    Control the variation in a manner commensurate with the risk it represents to the process and product."

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