N.Y. Comp. Codes R. & Regs. tit. 10, § 80.135
(b) The department will review the plan submitted by the not-for-profit corporation or government entity using the following standards:
(e) Individuals participating in the approved plan may obtain and possess hypodermic syringes and hypodermic needles without prescription from individuals authorized pursuant to subdivision (a) of this section provided that:
(g) An organization or entity authorized by the commissioner to conduct a hypodermic syringe and needle exchange program must adhere to policies and procedures developed by the department for the conduct of a hypodermic syringe and needle exchange. An approved plan may propose revisions to the department's policies and procedures to reflect the specific conditions under which the plan is providing services. Any proposed revision must be approved by the department prior to implementation. Such policies and procedures will include, but not be limited to:
(h) The following records of hypodermic syringes, hypodermic needles, participants and transactions shall be maintained by the organization or entity engaged in exchanging hypodermic syringes and hypodermic needles:
(j) An organization or entity functioning under a needle exchange plan approved under subdivision (a) of this section must provide periodic reports of activities to the department in a format and time period specified by the department which shall include, but not be limited to:
(l) An organization or entity functioning under a needle exchange plan approved under subdivision (a) of this section may be inspected by authorized representatives of the State Commissioner of Health as necessary to ensure compliance with the requirements of this section. An organization or entity found to be in violation of these regulations will receive written notification of the violation from the department and a time period, not to exceed 30 days from the date of written notification, to correct the violation. If the organization or entity continues to be in violation of these regulations after the date required for correction, the commissioner may terminate approval of the plan. The commissioner may also terminate the plan immediately if s/he determines that approval of the plan is no longer in the interest of public health.
An organization or entity will receive notification of the termination from the commissioner or his/her designee, and a time period not to exceed 60 days to appeal the termination by written submission to the commissioner or his/her designee requesting reconsideration of the termination.
(m) Any not-for-profit organization or government entity seeking to obtain, possess and furnish hypodermic syringes and hypodermic needles, without prescription, must submit a plan to the commissioner for approval, which must be in a format specified by the department, and will include, but not be limited to:
(14) overdose prevention education that specifically includes information about methods participants should use to prevent any adverse reactions from:
(n) The commissioner may approve programs with plans that do not include all of the elements specified in subdivision (m) of this section, provided that:
(3) the plan includes at least the following elements: