New Mexico Administrative Code
Title 20 - ENVIRONMENTAL PROTECTION
Chapter 3 - RADIATION PROTECTION
Part 4 - STANDARDS FOR PROTECTION AGAINST RADIATION
Section 20.3.4.412 - DOSE EQUIVALENT TO AN EMBRYO/FETUS

Universal Citation: 20 NM Admin Code 20.3.4.412

Current through Register Vol. 35, No. 6, March 26, 2024

A. The licensee or registrant shall ensure that the dose equivalent to the embryo/fetus during the entire pregnancy, due to the occupational exposure of a declared pregnant woman, does not exceed 0.5 rem (5 millisieverts) (see 20.3.4.446 NMAC for recordkeeping requirements).

B. The licensee or registrant shall make efforts to avoid substantial variation above a uniform monthly exposure rate to a declared pregnant woman so as to satisfy the limit in Subsection A of this section.

C. The dose equivalent to the embryo/fetus is the sum of:

(1) the dose equivalent to the embryo/fetus resulting from radionuclides in the embryo/fetus and radionuclides in the declared pregnant woman; and

(2) the deep dose equivalent that is most representative of the dose to the embryo/fetus from external radiation, that is, in the mother's lower torso region:
(a) if multiple measurements have not been made, assignment of the highest deep dose equivalent for the declared pregnant woman shall be the dose to the embryo/fetus, in accordance with Subsection C of 20.3.4.405 NMAC; or

(b) if multiple measurements have been made, assignment of the deep dose equivalent for the declared pregnant woman from the individual monitoring device which is most representative of the dose to the embryo/fetus shall be the dose to the embryo/fetus; assignment of the highest deep dose equivalent for the declared pregnant woman to the embryo/fetus is not required unless that dose is also the most representative deep dose equivalent for the region of the embryo/fetus.

D. If the dose equivalent to the embryo/fetus is found to have exceeded 0.5 rem (5 millisieverts), or is within 0.05 rem (0.5 millisievert) of this dose, by the time the woman declares the pregnancy to the licensee or registrant, the licensee or registrant shall be deemed to be in compliance with Subsection A of this section if the additional dose equivalent to the embryo/fetus does not exceed 0.05 rem (0.5 millisievert) during the remainder of the pregnancy.

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