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Quality Control Laboratory Compliance - cGMPs and GLPs: One and a Half-day In-person Seminar

17 - 18 October 2013, Boston, United States


Introduction
Course Description:
FDA inspection and oversight of quality control (QC) laboratories are essential elements of the agency's evaluation of the compliance status of regulated companies representing multiple industries - pharmaceuticals, biologics, medical devices, as well as foods and cosmetics - as well as the contract QC laboratories which service these industries. Lack of compliance can result in severe regulatory actions, criminal liability, fines, and the inability to obtain product approvals.

This course will examine the fundamental requirements for all QC laboratories subject to FDA inspection, recent trends from FDA inspection reports and enforcement actions. In addition, this course will include a list of relevant regulations and guidelines and demonstrate how quality control and quality assurance personnel can monitor industry practices to stay "current” with FDA requirements (cGMPs and GLPs).

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Venue
Boston Marriott Copley Place, MA

Boston Marriott Copley Place, MA, 110 Huntington Ave, Boston, 02116, United States

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Organised by
ComplianceOnline
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