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ce marking, ce mark approval, fda 510k submissions, fda approval, iso 13485, iso 13485:2003, regulatory affairs, fda GMP, medical device approvals, sfda, jpal, medical distributor, fda 483, medical device regulations, iso 14971, fda training, cgmp
Description :
Emergo Group helps medical device companies obtain regulatory approval to sell their products in the largest medical device markets worldwide. Services include US FDA 510(k) submissions, CE Marking approvals, ISO 13485, FDA GMP and more. Since 1997.
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