10 CFR § 35.7 Medical Use of Byproduct Material

§ 35.7 FDA, other Federal, and State requirements.

Current through Oct 5, 2026 · Read all of Part 35

⚠ 2 pending changes to Part 35

Nothing in this part relieves the licensee from complying with applicable FDA, other Federal, and State requirements governing radioactive drugs or devices.

← § 35.6 Provisions for the protection of human research subjects.§ 35.8 Information collection requirements: OMB approval. →