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HUM-MOLGEN
-> Events
-> Courses and Workshops |
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December 19, 2013 |
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Center for Professional Innovation & Education, Inc., Malvern, PA
Mar. 5 & 6, 2014
This course discusses the FDA’s regulatory authority for approving medical devices prior to marketing and the compliance programs used in enforcing its authorities during the manufacture and post-marketing reporting systems. It also provides FDA strategies towards inspections of manufacturing sites, and compliance actions that may result from these inspections. The course provides the attendees with the most important regulatory resource materials needed to understand agency policies and enforcement actions. Issues to be covered include: - Structure of the FDA and current FDA regulatory compliance practices - how to work with FDA investigators
- The regulatory approval process – "what the FDA is looking for" in 510ks, PMAs and other pre-approval applications
- The scope of FDA’s compliance programs, policies and potential enforcement actions
- Discussion of post-marketing notification and reporting programs
- Strategies for development of an in-house compliance program for GMPs which ensure successful inspectional outcomes
- Recent FDA enforcement statistics
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.
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Organized by:
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Center for Professional Innovation & Education |
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Invited Speakers:
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Contact info@cfpie.com for a list of course instructors
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Deadline for Abstracts:
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n/a
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Registration:
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http://www.cfpie.com/showitem.aspx?productid=020&source=hummolgen
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E-mail:
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info@cfpie.com
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