21 C.F.R. · Food and Drugs
21 C.F.R. § 812.18

Import and export requirements.

Title 21 C.F.R. ● ACTIVE Primary Source
Regulatory Text

21 C.F.R. § 812.18 — Import and export requirements.

§ 812.18 Import and export requirements. (a) Imports. In addition to complying with other requirements of this part, a person who imports or offers for importation an investigational device subject to this part shall be the agent of the foreign exporter with respect to investigations of the device and shall act as the sponsor of the clinical investigation, or ensure that another person acts as the agent of the foreign exporter and the sponsor of the investigation. (b) Exports. A person exporting an investigational device subject to this part shall obtain FDA's prior approval, as required by section 801(e) of the act or comply with section 802 of the act. [45 FR 3751, Jan. 18, 1980, as amended at 62 FR 26229, May 13, 1997]

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21 C.F.R. § 812.18
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The regulatory text of 21 C.F.R. § 812.18 is reproduced from the official Code of Federal Regulations as published by the Office of the Federal Register and the National Archives and Records Administration.
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