N.J.S.A. 26:2-103.6 — Central registry of newborns at risk of hearing loss.

26:2-103.6 Central registry of newborns at risk of hearing loss. 6. a. The commissioner shall establish a central registry of newborns identified as having or being at risk of developing a hearing loss. The information in the central registry shall be used for the purposes of compiling statistical information and providing follow-up counseling, intervention and educational services to the parents of the newborns listed in the registry. b. A hospital, birthing center or health care professional who performs testing required by this act shall report the results of such testing when a hearing loss is indicated to the department in a manner and on forms prescribed by the commissioner. L.2001,c.373,s.6.

This is the verbatim text of N.J.S.A. 26:2-103.6, retrieved from the New Jersey Legislature's public statute corpus. Statutes are amended periodically — for the most current version, check the external source link above. Kyzer is not a law firm and this page is not legal advice.