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Regulatory support for importers, authorized representatives and distributors
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Free sale certificate
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Support and procedures for US FDA records:
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Classification
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513 (g)
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De Novo Process
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Q-Submission Program
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Submission Issue Request (SIR)
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510(k) Premarket Notification
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Premarket Approval (PMA, 21 CFR 814)
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Product registration in third countries
Import / Export
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