Section 223.21. In vitro testing

A veterinarian who uses radioactive material for in vitro testing shall comply with 10 CFR 31.11 (relating to general license for use of by-product material for certain in vitro clinical or laboratory testing) but is exempt from 10 CFR Part 20 Subpart K (relating to waste disposal).

The provisions of this § 223.21 adopted December 18, 1987, effective December 19, 1987, 17 Pa.B. 5235; amended June 19, 1992, effective June 20, 1992, 22 Pa. B. 3135; amended November 17, 1995, effective November 18, 1995, 25 Pa.B. 5085; amended July 16, 2004, effective July 17, 2004, 34 Pa.B. 3823. Immediately preceding text appears at serial page (282396).

Notation

Authority

The provisions of this § 223.21 issued under section 302 of the Radiation Protection Act (35 P. S. § 7110.302); and section 1920-A of The Administrative Code of 1929 (71 P. S. § 510-20); amended under the Radiation Protection Act (35 P. S. § § 7110.101—7110.703); and the Low-Level Radioactive Waste Disposal Act (35 P. S. § § 7130.101—7130.906); and sections 301 and 302 of the Radiation Protection Act (35 P. S. § § 7110.301 and 7110.302); and section 1920-A of The Administrative Code of 1929 (71 P. S. § 510-20).