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Date: 11th June, 2008

Location: web seminar, USA

Summary:
Clinical, Pharmaceutical, Water - Training

Although a Contamination Control Master Plan (CCMP) is not a required document, it has been used increasingly by companies to help organize and streamline all of the required contamination control processes. The CCMP defines how a company mitigates the risks of specific contaminants for their products, and identifies the key control and monitoring points as well as responsibilities within the organization.

This live and comprehensive web seminar will concentrate on the value of creating a master plan for contamination risks within a GMP manufacturing company. It will provide a high-level overview of what a CCMP is, as well as its content and scope, and will provide participants with a thorough listing of areas to consider.

Key Discussion Points will include:
What is a CCMP?
Why is a CCMP valuable to my company?
What is defined in the CCMP?
How is the CCMP controlled and updated?
How is the CCMP implemented?
Who contributes to the CCMP?

Learning Benefits - Upon completion of this course, participants will have a better understanding of:
Identifying the contamination concerns for your company
Identifying the controls necessary to mitigate contamination concerns
Establishing a written plan
Taking a holistic approach to contamination control
Achieving synergy among control programs
Providing clear guidance to your organization