Rule 15-21-78-1.6.10 - Mammography X-Ray Systems - Adoption by reference of several sections in 21 Code of Federal Regulations Part 900 Subpart B Section 900.12 21 Code of Federal Regulations § 900.12(b), § 900.12(c), § 900.12(d), § 900.12(e)(1), § 900.12(e)(2), § 900.12(e)(3), § 900.12(e)(4), § 900.12(e)(5), § 900.12(e)(6), § 900.12(e)(7), § 900.12(e)(8), § 900.12(e)(9), § 900.12(e)(10), § 900.12(e)(11), § 900.12(e)(12), § 900.12(f)(1), § 900.12(f)(2), and § 900.12(i) are adopted by reference as they exist on May 11, 2017, with the following exceptions:
1. Medical Records and Mammography Reports. In addition to the requirements of 21 Code of Federal Regulations § 900.12(c), a. Language in mammography reports and lay letters provided to patients receiving mammogram services furnished by the entity performing the mammography services directly to patients under the federal Mammography Quality Standards Act, 42 USC Section 263b shall be in compliance with the U.S. Food & Drug Administration's Mammography Quality Standards Act.b. Entities providing mammogram services shall consult guidelines and standards developed by the American College of Radiology, the American College of Obstetricians and Gynecologists and the American Cancer Society when developing any additional information the entity deems necessary for inclusion in mammography reports and lay letters. Any additional information provided in the report shall be evidence-based, consistent with accepted medical standards, and with the U.S. Food & Drug Administration's Mammography Quality Standards Act. Entities shall conduct an annual review of any forms provided to ensure compliance with FDA requirements.15 Miss. Code. R. 21-78-1.6.10
Miss. Code Ann. § 45-14-11