§ 32.72 - Manufacture, preparation, or transfer for commercial distribution of radioactive drugs containing byproduct material for medical use under part 35.

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The applicant commits to the following labeling requirements:

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A copy of each individual's certification by a specialty board whose certification process has been recognized by the Commission or an Agreement State as specified in § 35.55(a) of this chapter; or

A licensee shall satisfy the labeling requirements in paragraph (a)(4) of this section.