New Jersey § 45:14-67

§ 45:14-67.

a. A pharmacist licensed pursuant to P.L.2003, c. 280 ( C.45:14-40 et seq. ) shall be authorized to order and cause to be administered to any person any test

for the SARS-CoV-2 (COVID-19) or COVID-19 antibodies that the federal Food and Drug

Administration granted emergency use authorization or approval, provided that: (1) the manufacturer of the test is registered with the federal Food and Drug Administration

and is included in the Establishment Registration and Device Listing database maintained

by the federal Food and Drug Administration; (2) the place of manufacture provides reasonable assurance prior to or at the time

of shipment that the test is genuine; and (3) the pharmacy practice site distributes personal protection equipment to all pharmacy

staff and establishes protocols and procedures to ensure that all persons presenting

at the pharmacy for any reason, including to request testing for COVID-19, maintain

social distancing appropriate to prevent transmission of COVID-19, and complies with

any other applicable requirements that the New Jersey Board of Pharmacy may establish. For the purposes of this section, causing a test to be administered shall include

collecting a specimen, or overseeing the collection of a specimen, and causing the

specimen to be sent to a laboratory with the capacity to perform the test. The laboratory shall be authorized under federal and State law to perform the test,

including, but not limited to, the federal “Clinical Laboratory Improvement Amendments

of 1988 (CLIA),” Pub.L.100-578 ( 42 U.S.C. s.263a ), the “New Jersey Clinical Laboratory Improvement Act,” P.L.1975, c. 166 ( C.45:9-42.26 et seq. ), and associated regulations. If the test which is administered is one for which the analysis can be performed

at a CLIA-waived facility, and if the pharmacy at which the specimen is collected

has a CLIA waiver, then the test may be conducted at that pharmacy. In all other cases, the test shall be conducted at an off-site laboratory, which

laboratory shall report the results of the test to the pharmacist who ordered or administered

the test. b. If an individual tests positive for COVID-19 using a test administered by a pharmacist

pursuant to subsection a. of this section, the pharmacist shall advise the patient

on self-isolation guidance and provide the individual with any necessary resources,

such as the COVID-19 Home Care Guide developed by the New Jersey Department of Health,

except that, if the patient is a member of a group that is at high risk for health

complications from COVID-19 or is experiencing symptoms of a severe adverse reaction

to COVID-19, the pharmacist shall also advise the patient to promptly seek treatment

at a hospital or contact the patient's health care provider. The pharmacist shall ensure compliance with all other State and federal requirements

concerning a positive test for COVID-19, including applicable reporting and data collection

requirements.