N.Y. Comp. Codes R. & Regs. tit. 8, § 66.5
(2) Phase two therapeutic pharmaceutical agents shall mean:
(5) Temporary evaluation committee shall mean that committee appointed by the Commissioner of Education to advise the commissioner in the evaluation of optometric use of therapeutic pharmaceutical agents, pursuant to section 3 of chapter 517 of the Laws of 1995.
(b) Certification requirements.
(2) Phase two therapeutic pharmaceutical agents. To receive a certificate issued by the department to use phase two therapeutic pharmaceutical agents, an optometrist shall be licensed in New York and certified in the use of phase one therapeutic pharmaceutical agents, and meet the clinical training requirements set forth in paragraph (c)(2) of this section and the examination requirements set forth in subdivision (d) of this section. After certification, such phase two therapeutic pharmaceutical agents shall be used in accordance with the provisions of article 143 of the Education Law.
(c) Clinical training requirements for certification.
(1) To meet the clinical training requirements for certification in the use of phase one therapeutic pharmaceutical agents, the applicant shall present satisfactory evidence of either:
(2) To meet the clinical training requirements for certification in the use of phase two therapeutic pharmaceutical agents, the applicant shall present satisfactory evidence of either:
(d) Examination. To meet the examination requirement for either certification in the use of phase one therapeutic pharmaceutical agents or certification in the use of phase two therapeutic pharmaceutical agents, the applicant shall present evidence of successful completion of:
(2) an examination determined by the State Board for Optometry to be equivalent in scope and content to the ocular diseases portion of the examination of the National Board of Examiners in Optometry.
(e) Reporting requirement.
An optometrist certified to use phase two therapeutic pharmaceutical agents shall file with the temporary evaluation committee a phase two report for each patient treated with phase two therapeutic pharmaceutical agents within seven days following the initial and each subsequent visit by the same patient. The report shall be in a form developed by the temporary evaluation committee and approved by the commissioner.
(a) Definitions.
As used in this section: