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Effective Document Management for the Pharmaceutical, Biotech, & Medical Device Industries
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Effective Document Management for the Pharmaceutical, Biotech, & Medical Device Industries

8/24/2015 to 8/25/2015
When: August 24-25, 2015
Where: The Hilton Los Angeles Airport (LAX)
5711 West Century Boulevard
Los Angeles, California  90045
United States
Presenter: The Center for Professional Innovation & Education, Inc.
Contact: Olivia Carlin
610-648-7550

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Effective Document Management for the Pharmaceutical, Biotech, & Medical Device Industries

If you didn’t write it down, it didn’t happen! This is the position of the FDA and most regulatory agencies internationally. Good documentation is vital for doing business in the regulated world from discovery through marketplace. It is also important for due diligence and regulatory inspections, and is necessary for the success of your products and services. While the regulations tell you what you must do, they don’t tell you how. Based on industry best practices, this course clarifies how to refine your existing system, create a new one, or prepare to transition from a manual system to electronic controls.

This course also addresses what documents you need to control, what documentation you need to support your actual system and how to keep your documents current and compliant.

This course has been pre-approved by the Regulatory Affairs Professionals Society (RAPS) as eligible for 12 credits towards a participant's RAC recertification upon full completion.

Learn more about the course and register.

CfPIE is a preferred provider and offers MichBio members a 15% discount on course registration fees. Click here for more information.

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