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  • Regulatory support for importers, authorized representatives and distributors

  • Free sale certificate

  • Support and procedures for US FDA records:

    • Classification

    • 513 (g)

    • De Novo Process

    • Q-Submission Program

    • Submission Issue Request (SIR)

    • 510(k) Premarket Notification

    • Premarket Approval (PMA, 21 CFR 814)

  • Product registration in third countries

Import / Export

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