Developing an Environmental Monitoring Strategy for a Non-Sterile and Aseptic Processing Area | October 5, 2015 8:30 AM - October 6, 2015 4:00 PM |

Developing an Environmental Monitoring Strategy for a Non-Sterile and Aseptic Processing Area

Event Summary

October 5, 2015 - October 6, 2015
San Francisco, CA 94108
October 5, 2015 8:30 AM
October 6, 2015 4:00 PM
[email protected]
Click here to Visit


Course Description:
Environmental monitoring of non-sterile and aseptic processing areas (controlled/classified environments) and utility systems is required to maintain compliance per EU/FDA/Health Canada requirements. When a new or remodeled controlled and/or classified manufacturing area is established, a validation plan is needed to determine manufacturing surfaces, airborne testing (ISO 14644) and the utility monitoring that is required. This testing may extend to the media, personnel, incubators, refrigerators, development of SOPs, etc. The program will involve the DQ, IQ, OQ and PQ of the site and all of its equipment. Since the facility’s environmental and utility plan must be established and in compliance prior to the initiation of manufacturing, an extensive Gantt chart is a prerequisite to assure all activities are completed in a predetermined order and that the earliest possible date for initiation of production may be met.

The necessary regulatory documents also need to be in place and translated into the various SOPs. Significant source documents include ISO 14644, Annex 1 (revised March 2009), FDA’s Aseptic Processing Guidance document, USP (current version), and USP<1111> (for non-sterile products), etc.

The highly interactive two day seminar will explore and define the necessary elements in the development and implementation of an environmental monitoring strategy for a non-sterile and an aseptic processing area to include utility systems (controlled and controlled/classified environment). It will assist in assuring that your organization is maintaining itself within a cGMP compliance framework. Case studies that include Warning Letters will be discussed to illustrate regulatory environmental issues.

Learning Objectives:
Upon completing this course on developing environmental monitoring strategy participants will:

Assure their understanding of the fundamentals of an environmental monitoring program
Be able to identify the key elements
Understand how the regulations impact their cGMP non-sterile or aseptic processing areas and their "Controlled" and "Classified" environment
Understanding the various inspection approaches to monitoring a "Controlled" and "Classified" environment
Learn how to determine the regulatory requirements required for an environmental monitoring program
Be able to develop and initiate the use of a purified water, WFI and steam system
Recognize the issues of their water system before the system is commissioned
Learn how to use Failure Mode Effects Analyses to determine the critical sampling locations, appropriate sampling methodologies and frequencies for both environmental and utility systems
Be able to develop DQ/IQ/OQ/PQ requirements
Learn how to determine appropriate Alert and Action Levels for different ISO and water classifications
Understand the movement from a “paper” method of data trending

Who will Benefit:
Quality professionals
Regulatory professionals
Compliance professionals
Manufacturing engineers
Quality engineers
Quality auditors
Quality Control
Document control specialists

For Registration -

Note: Use coupon code 232082 and get 10% off on registration.


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