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| Monday, 23 February 2009 12:27 | |
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Are You Ready For The FDA or for a DAMAS third-party audit?
Domestic or foreign manufacturers of dental appliances are required by the Food and Drug Administration (FDA) to have "a quality system for the design, manufacture, packaging, labeling, storage, installation, and servicing of finished medical devices intended for commercial distribution in the United States." Refer to http://www.fda.gov/ , Title 21, Part 820 for the regulation in its entirety. The federal regulation, Title 21, Part 820 requires: that various specifications and controls be established for devices; that devices be designed under a quality system to meet these specifications; that devices be manufactured under a quality system; that finished devices meet these specifications; that devices be correctly installed, checked and serviced; that quality data be analyzed to identify and correct quality problems; and, that complaints be processed.
Specifically your Quality System should address the following:
- Determination of applicability and FDA registration (manufacture of Class II medical devices such as sleep apnea and snore guards requires registration; domestic labs outsourcing to offshore labs (and the offshore labs themselves) and labs that are re-packagers and re-labelers must register with FDA
- Assignment of management responsibility
- Defining of purchasing controls
- Identification/traceability of patient contact materials
- Production and process controls
- Acceptance of final product
- Review of Non-conforming product
- Corrective and Preventive Action procedures
- Control of Labeling and Packaging
- Handling, Storage, Distribution and Installation of materials and finished items
- Records retention and control system
Contact us for a quote on any of these services.
The Lean Quality Advantage
SafeLink Consulting can assist you in implementing a Quality System that incorporates Lean manufacturing principles. We will help you in mapping your work process’ flow in order to identify areas for improvement, such as, better technology and the elimination of waste, including time and materials. We will train key personnel on what it takes to meet FDA requirements. We provide all the tools necessary to customize a Quality Manual, Standard Operating Procedures, sample forms, and progress calls to keep you focused. We will help you every step of the way.

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