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For medical device companies that provide their products in the U.S., RJR Consulting handles the submission of 510K’s,PreMarket Approval (PMA’s) and DeNovo applications to FDA. It takes care of similar processes for enterprises that wish to establish their products in ex-U.S. countries. Another vital criterion, required to operate a facility in countries across Europe, Canada, Australia and others. that some medical device manufacturing enterprises may not have is ISO 13485 certification. This GMP certificate ensures a comprehensive quality management system for the design and manufacture of medical devices exists. RJR Consulting helps companies acquire ISO 13485 certification by conducting mock audits of the medical device manufacturing facility before the Certified Body / Health Authority comes and performs the actual inspection.![]()
It's a combination of understanding the movement of the client's needs, their geographic interests, and helping them to be able to stay ahead of the competition
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Company
RJR Consulting, Inc
Headquarters
Columbus, Oh
Management
Robert Russell, President & CEO
Description
RJR Consulting helps its clients expand their global geographical presence. It does so by providing them regulatory supportand assisting them in developing a new market in the targeted country, without the need for them to set up an office locally.
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