2011 - Introduction to Contamination Control Master Plans - Webinar By GlobalCompliancePanel

Why you should attend: 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.

Areas Covered in the Session:
What is a CCMP and how is it valuable to my company?
What topics are covered in the CCMP and to what extent?
How is the CCMP controlled and updated?
How is the CCMP implemented?
Who contributes to the CCMP?
Who Will Benefit:
QA personnel
Regulatory personnel
Operations managers
Microbiologists
R&D Scientists
Validation Personnel
Training departments
Consultants

Price List:
Live : $245.00
Corporate live : $995.00
Recorded : $295.00

webinars-AT-globalcompliancepanel.com
http://www.globalcompliancepanel.com

Phone: 800-447-9407
Fax: 302-288-6884