MIJ Enterprises presents a new online seminar “Contamination Control Master Plans” May 20, 2009.

Feb. 19, 2011 - PRLog -- Learn from industry experts how to create and use a Contamination Control Master Plan (CCMP) to help organize and streamline all required contamination control elements to ensure easy compliance.

Manufacturers of human medical products have established myriad control programs to comply with FDA regulations regarding control of product contaminants.  However, due to variable emphasis being placed on each of these control elements by FDA auditors, most manufacturers have developed their programs in a piecemeal fashion.  Thus, each element in a manufacturer’s control program has been implemented without regard for the effect of the other elements.  As a result, potential complimentary synergies between control elements have typically been overlooked while gaping compliance issues may exist.  A Contamination Control Master Plan (CCMP) is critical to help organize and streamline all of the required contamination control elements to ensure easy compliance. A CCMP defines to your organization, as well as to auditors, how you mitigate the risks of the specific contaminants for your products.  

This live web seminar concentrates on the value of creating a master plan for contamination risks within a GMP manufacturing company.  It provides an introduction to the creation, implementation, and maintenance of a Contamination Control Master Plan.

Learning Benefits:
•   Achieve satisfactory inspections more easily.
•   Higher assurance of new medical product approvals.
•   Minimize nonconformances.
•   Reduce rates of batch rework and rejections.
•   Avoid product recalls.
•   Identify and control the key contamination concerns for your company.
•   Take a holistic approach to contamination control.
•   Achieve synergy among control programs.

Who can benefit:
QA managers, regulatory affairs, operations managers, microbiologists, R&D scientists, validation professionals, training departments, consultants

Registration Information:
   http://www.globalcompliancepanel.com/control/w_product/~p...

   http://www.mijenterprises.embarqspace.com/#/upcoming-even...

MIJ Enterprises is a full-service consulting firm specializing in GMP Compliance, Validation, and Cleanroom services for the pharmaceutical, biotech, medical device, and medical diagnostic cGMP/cGLP industries. http://www.mijenterprises.embarqspace.com

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MIJ Enterprises, LLC, is a full-service consulting firm specializing in GMP Consulting, Validation, and Cleanroom services for your pharmaceutical, biotech, medical device, and medical diagnostic cGMP/cGLP industries.