Section He-P 4035.17 - Possession, Use, Calibration, and Check of Dose Calibrators(a) For direct measurements performed in accordance with He-P 4035.19, a licensee shall possess and use instrumentation to measure the activity of unsealed byproduct materials before it is administered to each patient or human research subject.(b) A licensee shall calibrate the instrumentation required in He-P 4035.17(a) in accordance with nationally recognized standards or the manufacturer's instructions.(c) A licensee shall retain a record of each instrument calibration for 3 years. The records shall include: (1) The model and serial number of the instrument;(2) The date of the calibration;(3) The results of the calibration; and(4) The name of the individual who performed the calibration.N.H. Admin. Code § He-P 4035.17
(See Revision Note at part heading for He-P 4035) #6942, eff 2-1-99; ss by #8800, INTERIM, eff 2-1-07, EXPIRED: 7-31-07
New. #8959, eff 8-7-07
Amended by Volume XXXV, Number 32 Filed August 13, 2015, Proposed by #10897, Effective 7/22/2015, Expires1/18/2016.Amended by Volume XXXVI Number 01, Filed January 7, 2016, Proposed by #11011, Effective 1/15/2016, Expires 1/15/2026.Amended by Volume XL Number 24, Filed June 11, 2020, Proposed by #13048, Effective 6/2/2020, Expires 6/2/2030.Amended by Volume XLII Number 45, Filed November 10, 2022, Proposed by #13473, Effective 10/25/2022, Expires 10/25/2032