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needed to prevent the transmission of a reportable communicable disease
that is prevalent in New York state; or (ii) is a recommended immuniza-
tion for such patients who: (A) meet age requirements, (B) lack documen-
tation of such immunization, (C) lack evidence of past infection, or (D)
have an additional risk factor or another indication as recommended by
[the advisory committee on immunization practices of the centers for
disease control and prevention] NATIONALLY RECOGNIZED CLINICAL PRACTICE
GUIDELINES. PROVIDED, HOWEVER, THAT ANYONE ADMINISTERING IMMUNIZATIONS
FOR COVID-19 WITHIN THEIR LAWFUL SCOPE OF PRACTICE SHALL ADMINISTER SUCH
IMMUNIZATION IF A PATIENT: (A) MEETS AGE REQUIREMENTS; (B) DOES NOT HAVE
A HISTORY OF ADVERSE REACTION TO SUCH IMMUNIZATION OR ANY INGREDIENT
THEREOF; (C) MEETS REQUIREMENTS UNDER WHICH THE FOOD AND DRUG ADMINIS-
TRATION HAS DETERMINED THE IMMUNIZATION IS SAFE; AND (D) MEETS OTHER
REQUIREMENTS AS DETERMINED BY THE COMMISSIONER OF HEALTH; WITHOUT
CONSIDERATION OR INQUIRY OF ANY OTHER CRITERIA OR GUIDELINES, INCLUDING
THOSE OF THE ADVISORY COMMITTEE ON IMMUNIZATION PRACTICES OF THE CENTERS
FOR DISEASE CONTROL AND PREVENTION OR A SUCCESSOR. FOR THE PURPOSES OF
THIS SECTION, THE ABSENCE OF ANY ISSUANCE OF ADDITIONAL GUIDELINES FROM
THE COMMISSIONER OF HEALTH SHALL CREATE A PRESUMPTION THAT THERE ARE NO
ADDITIONAL REQUIREMENTS TO SATISFY THE CRITERIA FOR ADMINISTRATION OF
IMMUNIZATION FOR COVID-19. Nothing in this subdivision shall authorize
unlicensed persons to administer immunizations, vaccines or other drugs,
NOR AUTHORIZE LICENSED PERSONS TO ADMINISTER IMMUNIZATIONS, VACCINES OR
OTHER DRUGS IN VIOLATION OF ANY STATE OR FEDERAL LAW.
§ 2. Subdivision 7 of section 6909 of the education law, as amended by
chapter 555 of the laws of 2021, is amended to read as follows:
7. A certified nurse practitioner may prescribe and order a patient
specific order or non-patient specific regimen to a licensed pharmacist,
pursuant to regulations promulgated by the commissioner, and consistent
with the public health law, for: (a) administering immunizations to
prevent influenza to patients two years of age or older; and (b) admin-
istering immunizations to prevent pneumococcal, acute herpes zoster,
hepatitis A, hepatitis B, human papillomavirus, measles, mumps, rubella,
varicella, COVID-19, meningococcal, tetanus, diphtheria or pertussis
disease and medications required for emergency treatment of anaphylaxis
to patients eighteen years of age or older; and (c) administering other
immunizations recommended by [the advisory committee on immunization
practices of the centers for disease control and prevention] NATIONALLY
RECOGNIZED CLINICAL PRACTICE GUIDELINES for patients eighteen years of
age or older if the commissioner of health in consultation with the
commissioner determines that an immunization: (i) (A) may be safely
administered by a licensed pharmacist within their lawful scope of prac-
tice; and (B) is needed to prevent the transmission of a reportable
communicable disease that is prevalent in New York state; or (ii) is a
recommended immunization for such patients who: (A) meet age require-
ments, (B) lack documentation of such immunization, (C) lack evidence of
past infection, or (D) have an additional risk factor or another indi-
cation as recommended by [the advisory committee on immunization prac-
tices of the centers for disease control and prevention] NATIONALLY
RECOGNIZED CLINICAL PRACTICE GUIDELINES. PROVIDED, HOWEVER, THAT ANYONE
ADMINISTERING IMMUNIZATIONS FOR COVID-19 WITHIN THEIR LAWFUL SCOPE OF
PRACTICE SHALL ADMINISTER SUCH IMMUNIZATION IF A PATIENT: (A) MEETS AGE
REQUIREMENTS; (B) DOES NOT HAVE A HISTORY OF ADVERSE REACTION TO SUCH
IMMUNIZATION OR ANY INGREDIENT THEREOF; (C) MEETS REQUIREMENTS UNDER
WHICH THE FOOD AND DRUG ADMINISTRATION HAS DETERMINED THE IMMUNIZATION
IS SAFE; AND (D) MEETS OTHER REQUIREMENTS AS DETERMINED BY THE COMMIS-
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SIONER OF HEALTH; WITHOUT CONSIDERATION OR INQUIRY OF ANY OTHER CRITERIA
OR GUIDELINES, INCLUDING THOSE OF THE ADVISORY COMMITTEE ON IMMUNIZATION
PRACTICES OF THE CENTERS FOR DISEASE CONTROL AND PREVENTION OR A SUCCES-
SOR. FOR THE PURPOSES OF THIS SECTION, THE ABSENCE OF ANY ISSUANCE OF
ADDITIONAL GUIDELINES FROM THE COMMISSIONER OF HEALTH SHALL CREATE A
PRESUMPTION THAT THERE ARE NO ADDITIONAL REQUIREMENTS TO SATISFY THE
CRITERIA FOR ADMINISTRATION OF IMMUNIZATION FOR COVID-19. Nothing in
this subdivision shall authorize unlicensed persons to administer immun-
izations, vaccines or other drugs, NOR AUTHORIZE LICENSED PERSONS TO
ADMINISTER IMMUNIZATIONS, VACCINES OR OTHER DRUGS IN VIOLATION OF ANY
STATE OR FEDERAL LAW.
§ 3. Subparagraph 1 of paragraph a of subdivision 22 of section 6802
of the education law, as amended by chapter 802 of the laws of 2022, is
amended to read as follows:
(1) the direct application of an immunizing agent to adults, whether
by injection, ingestion, inhalation or any other means, pursuant to a
patient specific order or non-patient specific regimen prescribed or
ordered by a physician or certified nurse practitioner, for: immuniza-
tions to prevent influenza, pneumococcal, acute herpes zoster, hepatitis
A, hepatitis B, human papillomavirus, measles, mumps, rubella, varicel-
la, COVID-19, meningococcal, tetanus, diphtheria or pertussis disease
and medications required for emergency treatment of anaphylaxis; and
other immunizations recommended by [the advisory committee on immuniza-
tion practices of the centers for disease control and prevention]
NATIONALLY RECOGNIZED CLINICAL PRACTICE GUIDELINES for patients eighteen
years of age or older if the commissioner of health in consultation with
the commissioner determines that an immunization: (i)(A) may be safely
administered by a licensed pharmacist within their lawful scope of prac-
tice; and (B) is needed to prevent the transmission of a reportable
communicable disease that is prevalent in New York state; or (ii) is a
recommended immunization for such patients who: (A) meet age require-
ments, (B) lack documentation of such immunization, (C) lack evidence of
past infection, or (D) have an additional risk factor or another indi-
cation as recommended by [the advisory committee on immunization prac-
tices of the centers for disease control and prevention] NATIONALLY
RECOGNIZED CLINICAL PRACTICE GUIDELINES. PROVIDED, HOWEVER, THAT ANYONE
ADMINISTERING IMMUNIZATIONS FOR COVID-19 WITHIN THEIR LAWFUL SCOPE OF
PRACTICE SHALL ADMINISTER SUCH IMMUNIZATION IF A PATIENT: (A) MEETS AGE
REQUIREMENTS; (B) DOES NOT HAVE A HISTORY OF ADVERSE REACTION TO SUCH
IMMUNIZATION OR ANY INGREDIENT THEREOF; (C) MEETS REQUIREMENTS UNDER
WHICH THE FOOD AND DRUG ADMINISTRATION HAS DETERMINED THE IMMUNIZATION
IS SAFE; AND (D) MEETS OTHER REQUIREMENTS AS DETERMINED BY THE COMMIS-
SIONER OF HEALTH; WITHOUT CONSIDERATION OR INQUIRY OF ANY OTHER CRITERIA
OR GUIDELINES, INCLUDING THOSE OF THE ADVISORY COMMITTEE ON IMMUNIZATION
PRACTICES OF THE CENTERS FOR DISEASE CONTROL AND PREVENTION OR A SUCCES-
SOR. FOR THE PURPOSES OF THIS SECTION, THE ABSENCE OF ANY ISSUANCE OF
ADDITIONAL GUIDELINES FROM THE COMMISSIONER OF HEALTH SHALL CREATE A
PRESUMPTION THAT THERE ARE NO ADDITIONAL REQUIREMENTS TO SATISFY THE
CRITERIA FOR ADMINISTRATION OF IMMUNIZATION FOR COVID-19. If the commis-
sioner of health determines that there is an outbreak of disease, or
that there is the imminent threat of an outbreak of disease, then the
commissioner of health may issue a non-patient specific regimen applica-
ble statewide.
§ 4. Paragraph (e) of subdivision 2 of section 6801 of the education
law, as amended by section 1 of part DD of chapter 57 of the laws of
2018, is amended to read as follows:
A. 9077 4
(e) administer the immunization or immunizations according to the most
current recommendations by [the advisory committee for immunization
practices (ACIP)] NATIONALLY RECOGNIZED CLINICAL PRACTICE GUIDELINES,
provided however, that a pharmacist may administer any immunization
authorized under this section when specified by a patient specific
order.
§ 5. Subdivision 4 of section 6801 of the education law, as amended by
section 1 of part DD of chapter 57 of the laws of 2018, is amended to
read as follows:
4. When administering an immunization in a pharmacy, the licensed
pharmacist shall provide an area for the immunization that provides for
a patient's privacy. The privacy area should include:
[a.] (A) a clearly visible posting of the most current ["Recommended
Adult Immunization Schedule" published by the advisory committee for
immunization practices (ACIP)] RECOMMENDED ADULT IMMUNIZATION SCHEDULE
ACCORDING TO NATIONALLY RECOGNIZED BEST PRACTICES; and
(b) education materials on influenza vaccinations for children as
determined by the commissioner and the commissioner of health.
§ 6. Section 6801 of the education law is amended by adding a new
subdivision 4-a to read as follows:
4-A. A PHARMACY WHICH OFFERS IMMUNIZATION APPOINTMENTS, INCLUDING BY
PHONE OR ONLINE, SHALL OFFER ALL IMMUNIZATIONS ACCORDING TO RECOMMENDA-
TIONS BY NATIONALLY RECOGNIZED CLINICAL PRACTICE GUIDELINES, AND WITHOUT
AN ADVANCE PRESCRIPTION. A PHARMACY SHALL NOT IMPOSE ANY LIMITATIONS OR
CRITERIA OTHER THAN THOSE SET FORTH IN SUBDIVISION TWENTY-TWO OF SECTION
SIXTY-EIGHT HUNDRED TWO OF THIS ARTICLE.
§ 7. Subparagraph 5 of paragraph f of subdivision 5 of section 2-d of
the education law, as added by section 1 of subpart L of part AA of
chapter 56 of the laws of 2014, is amended to read as follows:
(5) [uses] USE encryption technology to protect data while in motion
or in its custody from unauthorized disclosure using a technology or
methodology specified by the COMMISSIONER OF HEALTH OR secretary of the
United States department of health and human services in guidance issued
under Section 13402(H)(2) of Public Law 111-5.
§ 8. Paragraph (a) of subdivision 25 of section 206 of the public
health law, as added by chapter 563 of the laws of 2008, is amended to
read as follows:
(a) In assessing and reporting on the impact of section sixty-eight
hundred one of the education law, pursuant to subdivision four of such
section the commissioner may BUT SHALL NOT BE REQUIRED TO use: (1)
influenza vaccine supply data from the federal centers for disease
control and prevention; (2) pneumococcal vaccine supply data provided by
manufacturers and distributors of such vaccine; and (3) data from a
third party entity that engages in the collection of data and tracking
of pharmaceutical sales and distribution. Manufacturers and distributors
of pneumococcal vaccine shall provide or arrange for the timely
provision to the commissioner of such data as the commissioner may
reasonably request to complete the report. Provider and customer iden-
tifiable information submitted pursuant to this paragraph shall be
confidential, unless the information provider consents to its release or
the commissioner determines disclosure is necessary to respond to an
imminent public health emergency.
§ 9. Section 206 of the public health law is amended by adding a new
subdivision 32 to read as follows:
32. ANY RULES AND REGULATIONS OF THE DEPARTMENT IN EFFECT OF THE
EFFECTIVE DATE OF THIS SUBDIVISION WHICH REFERENCE OR DIRECT THE FOLLOW-
A. 9077 5
ING OF GUIDELINES OF THE UNITED STATES CENTERS FOR DISEASE CONTROL AND
PREVENTION OR ANY PART, PORTION OR COMMITTEE THEREOF SHALL BE DEEMED TO
REFER TO NATIONALLY RECOGNIZED BEST PRACTICES. FOR THE PURPOSES OF THIS
SUBDIVISION, AND ANY REFERENCES IN ANY OTHER STATUTE, THE TERM
"NATIONALLY RECOGNIZED CLINICAL PRACTICE" SHALL MEAN A CLINICAL
APPROACH, METHODOLOGY, OR STANDARD OF CARE THAT IS WIDELY ACCEPTED AND
UTILIZED BY LICENSED HEALTH CARE PROFESSIONALS ACROSS THE UNITED STATES,
BASED ON PEER-REVIEWED SCIENTIFIC EVIDENCE AND PROFESSIONAL CONSENSUS,
WHICH MAY NOT BE CONSISTENT WITH GUIDELINES ISSUED BY A FEDERAL AGENCY
OR OTHER ORGANIZATION IF SUCH GUIDELINES CONFLICT WITH PEER-REVIEWED
SCIENTIFIC EVIDENCE AND PROFESSIONAL CONSENSUS. THE COMMISSIONER MAY
ISSUE DETERMINATIONS OF NATIONALLY RECOGNIZED CLINICAL PRACTICE,
PROVIDED, HOWEVER, THAT THE ABSENCE OF SUCH A DETERMINATION SHALL NOT
IMPLY REQUIREMENT TO ADHERE TO GUIDELINES ISSUED BY A FEDERAL AGENCY OR
OTHER ORGANIZATION IF SUCH GUIDELINES CONFLICT WITH PEER-REVIEWED SCIEN-
TIFIC EVIDENCE AND PROFESSIONAL CONSENSUS.
§ 10. Subdivision 3 of section 266-a of the public health law, as
added by chapter 483 of the laws of 2014 and such section as renumbered
by chapter 653 of the laws of 2022, is amended to read as follows:
3. Consult with national vaccine and immunization policy making organ-
izations[, including but not limited to, the advisory committee on
immunization practices under the centers for disease control and
prevention, the national institute of health and the national institute
of allergy and infectious diseases] WHOSE POLICIES CONFORM TO NATIONALLY
RECOGNIZED CLINICAL PRACTICE;
§ 11. Subdivision 2 of section 1399-mm-3 of the public health law, as
added by section 1 of part EE of chapter 56 of the laws of 2020, is
amended to read as follows:
2. The commissioner is authorized to promulgate rules and regulations
governing the sale and distribution of carrier oils that are suspected
of causing acute illness [and have been identified as a chemical of
concern by the United States centers for disease control and
prevention]. Such regulations may, to the extent deemed by the commis-
sioner as necessary for the protection of public health, prohibit or
restrict the selling, offering for sale, possessing with intent to sell,
or distributing of carrier oils.
§ 12. Section 2170 of the public health law, as amended by chapter
109 of the laws of 2004, is amended to read as follows:
§ 2170. Hepatitis C; educational materials. The commissioner shall
develop and make available to physicians, other health care providers,
veterans and other persons at high risk for hepatitis C educational
materials, in written and electronic forms, on the diagnosis, treatment
and prevention of hepatitis C. Such materials shall include the recom-
mendations of [the federal Centers for Disease Control and Prevention
and any other person or entity] ANY PERSONS OR ENTITIES having knowledge
on hepatitis C, including the American Liver Foundation. Such materials
shall be written in terms which are understandable by members of the
general public.
§ 13. Subdivisions 1 and 3 of section 2312 of the public health law,
as amended by chapter 298 of the laws of 2019, are amended to read as
follows:
1. Notwithstanding any other provision of law and consistent with
section two thousand three hundred five of this title, a health care
practitioner (who is authorized under title eight of the education law
to diagnose and prescribe drugs for sexually transmitted chlamydia
trachomatis infection and other sexually transmitted infections, acting
A. 9077 6
within [his or her] THEIR lawful scope of practice) who diagnoses a
sexually transmitted chlamydia trachomatis infection or other sexually
transmitted infection in an individual patient may prescribe, dispense,
furnish, or otherwise provide prescription antibiotic drugs for the
sexually transmitted infections for which [the Centers for Disease
Control and Prevention recommends] NATIONALLY RECOGNIZED CLINICAL PRAC-
TICE GUIDELINES RECOMMEND the use of expedited partner therapy to that
patient's sexual partner or partners without examination of that
patient's partner or partners.
3. The commissioner shall promulgate rules and regulations concerning
the implementation of this section and shall also develop forms for
patients and their partners explaining expedited partner therapy for a
chlamydia trachomatis infection and other sexually transmitted
infections for which [the Centers for Disease Control and Prevention
recommends] NATIONALLY RECOGNIZED CLINICAL PRACTICE GUIDELINES RECOMMEND
the use of expedited partner therapy. Such forms shall be written in a
clear and coherent manner using words with common, everyday meanings.
§ 14. Paragraph c of subdivision 2 of section 2164 of the public
health law, as added by chapter 401 of the laws of 2015, is amended to
read as follows:
c. Every person in parental relation to a child in this state entering
or having entered seventh grade and twelfth grade or a comparable age
level special education program with an unassigned grade on or after
September first, two thousand sixteen, shall have administered to such
child an adequate dose or doses of immunizing agents against meningococ-
cal disease as recommended by [the advisory committee on immunization
practices of the centers for disease control and prevention] NATIONALLY
RECOGNIZED CLINICAL PRACTICE GUIDELINES, which meets the standards
approved by the United States public health service for such biological
products, and which is approved by the department under such conditions
as may be specified by the public health and planning council.
§ 15. Paragraph d of subdivision 1 and subdivision 8 of section 2165
of the public health law, as added by chapter 405 of the laws of 1989,
are amended to read as follows:
d. The term "immunization" means an adequate dose or doses of an
immunizing agent against measles, mumps and rubella [which meets the
standards approved by the United States public health service for such
biological products, and which is] approved by the state department of
health under such conditions as may be specified by the public health
council.
8. If any licensed physician or nurse practitioner certifies that such
immunization may be detrimental to the person's health or is otherwise
medically contraindicated PURSUANT TO NATIONALLY RECOGNIZED BEST PRAC-
TICES, the requirements of this section shall be inapplicable until such
immunization is found no longer to be detrimental to such person's
health or is no longer medically contraindicated.
§ 16. Subdivision 11-a of section 2168 of the public health law, as
amended by chapter 109 of the laws of 2023, is amended to read as
follows:
11-a. The commissioner, or in the city of New York, the commissioner
of the department of health and mental hygiene, may only share registry
information maintained by the department, or in the case of the citywide
immunization registry, the city of New York under the provisions of this
section [with the federal Centers for Disease Control and Prevention, or
successor agency] PURSUANT TO FEDERAL LAW OR AS DETERMINED BY THE
COMMISSIONER, for public health purposes in summary, statistical, aggre-
A. 9077 7
gate, or other form such that no individual person can be identified,
except that either such commissioner may disclose identifiable regis-
trant information to the federal Centers for Disease Control and
Prevention, or its successor agency, when the commissioner has deter-
mined that the disclosure is in the best interests of the registrant or
will contribute to the protection of public health and that the objec-
tive of the disclosure cannot be served by disclosure limited to de-i-
dentified information, or the federal health officials have committed in
writing not to redisclose to or share registrant information with any
other federal agency, including but not limited to the department of
homeland security, immigration and customs enforcement, customs and
border protection, or any successor agency, or any law enforcement agen-
cy; provided that either such commissioner may forgo the written commit-
ment if requiring written commitment would result in the actual with-
holding of federal funds.
§ 17. Subdivision 1 of section 2599-b of the public health law, as
amended by section 1 of part A of chapter 469 of the laws of 2015, is
amended to read as follows:
1. The program shall be designed to prevent and reduce the incidence
and prevalence of obesity in children and adolescents, especially among
populations with high rates of obesity and obesity-related health
complications including, but not limited to, diabetes, heart disease,
cancer, osteoarthritis, asthma, emphysema, chronic bronchitis, other
chronic respiratory diseases and other conditions. The program shall use
NATIONALLY RECOGNIZED CLINICAL PRACTICE recommendations and goals [of
the United States departments of agriculture and health and human
services, the surgeon general and centers for disease control and
prevention] in developing and implementing guidelines for nutrition
education and physical activity projects as part of obesity prevention
efforts. The content and implementation of the program shall stress the
benefits of choosing a balanced, healthful diet from the many options
available to consumers, without specifically targeting the elimination
of any particular food group, food product or food-related industry.
§ 18. Clauses (A) and (C) of subparagraph (i) of paragraph (a) of
subdivision 12 of section 2803 of the public health law, clause (A) as
amended by chapter 20 of the laws of 2023 and clause (C) as amended by
chapter 19 of the laws of 2022, are amended to read as follows:
(A) to update authorized family members and resident representatives
of infected residents at least once per day and upon a change in a resi-
dent's condition and at least once a week to update all residents and
authorized families and resident representatives on the number of
infections and deaths at the facility, and to update all residents,
authorized family members, and resident representatives at the facility
not later than five o'clock p.m. the next calendar day following the
detection of a confirmed infection of a resident or staff member, or at
such earlier time [as guidance from the federal centers for Medicaid and
medicare services or centers for disease control and prevention may
provide] IN ACCORDANCE WITH NATIONALLY RECOGNIZED BEST PRACTICES, by
electronic or such other means as may be selected by each resident,
authorized family member or resident representative; and
(C) a plan or procedure, consistent with [any guidance issued by the
federal centers for Medicaid and medicare services or centers for
disease control and prevention] NATIONALLY RECOGNIZED BEST PRACTICES,
for placement or grouping of residents within a facility to reduce tran-
smission of the pandemic disease during an infectious disease outbreak
in the residential health care facility; and
A. 9077 8
§ 19. Paragraph (a) of subdivision 5 of section 2803-j of the public
health law, as added by chapter 62 of the laws of 1996, is amended to
read as follows:
(a) The commissioner shall establish an immunization schedule for
newborn children. The immunization schedule shall chart out recommended
immunizations against certain diseases and illnesses and age-appropriate
times for the administration of each immunization. The immunization
schedule shall also include information on the importance of getting
children immunized at the recommended ages. The immunization schedule
shall also include the toll-free telephone number operated by the
department as part of its immunization education efforts. The immuniza-
tion schedule shall be in accordance with recommendations established by
the New York state department of health [and the immunization practices
advisory committee of the United States department of health and human
services].
§ 20. Subdivision 1 of section 2196 of the public health law, as added
by chapter 580 of the laws of 1999, is amended to read as follows:
1. The commissioner shall promulgate regulations relating to the
immunization requirements of this article, taking into consideration the
recommendations of [the centers for disease control and prevention]
NATIONALLY RECOGNIZED CLINICAL PRACTICE GUIDELINES.
§ 21. Subdivision 1 of section 2780 of the public health law, as added
by chapter 584 of the laws of 1988, is amended to read as follows:
1. "AIDS" means acquired immune deficiency syndrome[, as may be
defined from time to time by the centers for disease control of the
United States public health service].
§ 22. Subdivision 13 of section 131 of the social services law, as
added by chapter 61 of the laws of 1996, is amended to read as follows:
13. Social services districts shall provide all applicants and recipi-
ents of public assistance with children five years of age or less with
information and a schedule regarding age-appropriate immunizations for
children in accordance with [the recommendations of the department of
health and the immunization practices advisory committee of the United
States department of health and human services] NATIONALLY RECOGNIZED
BEST PRACTICES. The telephone number of the local county health depart-
ment shall be included on the immunization schedule.
§ 23. Paragraphs (q) and (ff) of subdivision 2 of section 365-a of the
social services law, paragraph (q) as amended by section 35 of part B of
chapter 58 of the laws of 2010, and paragraph (ff) as added by section 1
of part C of chapter 57 of the laws of 2019, are amended to read as
follows:
(q) diabetes self-management training services for persons diagnosed
with diabetes when such services are ordered by a physician, registered
physician assistant, registered nurse practitioner, or licensed midwife
and provided by a licensed, registered, or certified health care profes-
sional, as determined by the commissioner of health, who is certified as
a diabetes educator by the National Certification Board for Diabetes
Educators, or a successor national certification board, or provided by
such a professional who is affiliated with a program certified by the
American Diabetes Association, the American Association of Diabetes
Educators, the Indian Health Services, or any other national accredi-
tation organization approved by the [federal centers for medicare and
medicaid services] THE COMMISSIONER OF HEALTH; provided, however, that
the provisions of this paragraph shall not take effect unless all neces-
sary approvals under federal law and regulation have been obtained to
receive federal financial participation in the costs of health care
A. 9077 9
services provided pursuant to this paragraph. Nothing in this paragraph
shall be construed to modify any licensure, certification or scope of
practice provision under title eight of the education law.
(ff) evidence-based prevention and support services [recognized by the
federal Centers for Disease Control (CDC),] provided by a community-
based organization, and designed to prevent individuals at risk of
developing diabetes from developing Type 2 diabetes.
§ 24. Paragraph (b) of subdivision 1 of section 365-k of the social
services law, as amended by chapter 41 of the laws of 2023, is amended
to read as follows:
(b) The standards and guidelines established under this section for
providing non-invasive prenatal testing shall not limit availability and
coverage for a test based on the age of the pregnant patient, unless the
limit is explicitly called for by the generally accepted standards of
professional practice [or is otherwise recommended by safety communi-
cations or guidance issued by the United States food and drug adminis-
tration, the centers for Medicare and medicaid services, or the United
States department of health and human services].
§ 25. Clause (i) of subparagraph 2 of paragraph (d) of subdivision 4
of section 366 of the social services law, as added by section 2 of part
D of chapter 56 of the laws of 2013, is amended to read as follows:
(i) Medical assistance is available under this paragraph to persons
who are under sixty-five years of age, have been screened for breast
and/or cervical cancer under [the Centers for Disease Control and
Prevention breast and cervical cancer early detection program]
NATIONALLY RECOGNIZED CLINICAL PRACTICE GUIDELINES and need treatment
for breast or cervical cancer, and are not otherwise covered under cred-
itable coverage as defined in the federal public health service act;
provided however that medical assistance shall be furnished pursuant to
this clause only to the extent permitted under federal law, if, for so
long as, and to the extent that federal financial participation is
available therefor.
§ 26. Paragraph (d) of subdivision 1 and subdivision 4 of section 178
of the civil service law, as added by chapter 390 of the laws of 2005,
are amended to read as follows:
(d) "Significant risk of transmission" means the alleged conduct of or
actions taken by an assailant or any other action, situation or event
that occurs while a public protection official is performing [his or
her] THEIR official duties that has created a recognized and significant
risk of infection of a public protection official with the human immuno-
deficiency virus (HIV), as determined by the commissioner of health,
consistent with NATIONALLY RECOGNIZED CLINICAL PRACTICE guidelines,
protocols, and findings [of the United States centers for disease
control and prevention].
4. Guidelines. The commissioner of health shall issue guidelines to
facilitate the identification of circumstances potentially exposing a
public protection official to a significant risk of transmission of the
human immunodeficiency virus (HIV). Such guidelines shall be consistent
with NATIONALLY RECOGNIZED CLINICAL PRACTICE criteria [accepted by the
federal centers for disease control and prevention]. Such guidelines
shall also provide information regarding related counseling and testing
procedures available to such individuals.
§ 27. Subdivision 2 of section 930 of the labor law, as amended by
chapter 90 of the laws of 2015, is amended to read as follows:
2. "Mold" means any indoor multi-cellular fungi growth capable of
creating toxins that can cause pulmonary, respiratory, neurological or
A. 9077 10
other major illnesses after minimal exposure, as such exposure is
defined by [the environmental protection agency, centers for disease
control and prevention, national institute of health, or other] ANY
federal, state, or local agency OR ORGANIZATION AS DETERMINED BY THE
COMMISSIONER OF HEALTH AND organized to study and/or protect human
health.
§ 28. Paragraph 2 of subsection (d) of section 2611 of the insurance
law, as added by chapter 584 of laws of 1988, is amended to read as
follows:
(2) "AIDS" means acquired immune deficiency syndrome[, as may be
defined from time to time by the centers for disease control of the
United States public health service].
§ 29. Paragraphs (c) and (e) of subdivision 1 of section 2411 of the
public health law, as amended by section 5 of part A of chapter 60 of
the laws of 2014, are amended to read as follows:
(c) Consult with [the Centers for Disease Control and Prevention, the
National Institutes of Health, the Federal Agency For Health Care Policy
and Research, the National Academy of Sciences and other] organizations
or entities which may be involved in cancer research to solicit both
information regarding breast cancer research projects that are currently
being conducted and recommendations for future research projects;
(e) Solicit, receive, and review applications from public and private
agencies and organizations and qualified research institutions for
grants from the breast cancer research and education fund, created
pursuant to section ninety-seven-yy of the state finance law, to conduct
research or educational programs which focus on the causes, prevention,
screening, treatment and cure of breast cancer and may include, but are
not limited to mapping of breast cancer, and basic, behavioral, clin-
ical, demographic, environmental, epidemiologic and psychosocial
research. The board shall make recommendations to the commissioner, and
the commissioner shall, in [his or her] THEIR discretion, grant approval
of applications for grants from those applications recommended by the
board. The board shall consult with [the Centers for Disease Control and
Prevention, the National Institutes of Health, the Federal Agency For
Health Care Policy and Research, the National Academy of Sciences,]
breast cancer advocacy groups[,] and other organizations or entities
which may be involved in breast cancer research to solicit both informa-
tion regarding breast cancer research projects that are currently being
conducted and recommendations for future research projects. As used in
this section, "qualified research institution" may include academic
medical institutions, state or local government agencies, public or
private organizations within this state, and any other institution
approved by the department, which is conducting a breast cancer research
project or educational program. If a board member submits an application
for a grant from the breast cancer research and education fund, [he or
she] THEY shall be prohibited from reviewing and making a recommendation
on the application;
§ 30. Item (iv) of subparagraph (A) of paragraph 12 of subsection (i)
of section 3216 of the insurance law, as amended by chapter 357 of the
laws of 2010, is amended to read as follows:
(iv) Elsevier Gold Standard's Clinical Pharmacology; or other authori-
tative compendia as identified by the [Federal Secretary of Health and
Human Services or the Centers for Medicare & Medicaid Services (CMS)]
COMMISSIONER OF HEALTH; or recommended by review article or editorial
comment in a major peer reviewed professional journal.
A. 9077 11
§ 31. Item (ii) of subparagraph (E) of paragraph 17 of subsection (i)
of section 3216 of the insurance law, as amended by chapter 219 of the
laws of 2011, is amended to read as follows:
(ii) immunizations that have in effect a recommendation [from the
advisory committee on immunization practices of the centers for disease
control and prevention] PURSUANT TO NATIONALLY RECOGNIZED CLINICAL PRAC-
TICE GUIDELINES with respect to the individual involved;
§ 32. Item (ii) of subparagraph (E) of paragraph 8 of subsection (l)
of section 3221 of the insurance law, as amended by chapter 219 of the
laws of 2011, is amended to read as follows:
(ii) immunizations that have in effect a recommendation [from the
advisory committee on immunization practices of the centers for disease
control and prevention] PURSUANT TO NATIONALLY RECOGNIZED CLINICAL PRAC-
TICE GUIDELINES with respect to the individual involved;
§ 33. Item (iv) of subparagraph (A) of paragraph 12 of subsection (l)
of section 3221 of the insurance law, as amended by chapter 357 of the
laws of 2010, is amended to read as follows:
(iv) Elsevier Gold Standard's Clinical Pharmacology; or other authori-
tative compendia as identified by the [Federal Secretary of Health and
Human Services or the Centers for Medicare & Medicaid Services (CMS)]
COMMISSIONER OF HEALTH; or recommended by review article or editorial
comment in a major peer reviewed professional journal.
§ 34. Subparagraph (B) of paragraph 3 of subsection (j) of section
4303 of the insurance law, as added by chapter 219 of the laws of 2011,
is amended to read as follows:
(B) immunizations that have in effect a recommendation [from the advi-
sory committee on immunization practices of the centers for disease
control and prevention] PURSUANT TO NATIONALLY RECOGNIZED CLINICAL PRAC-
TICE GUIDELINES with respect to the individual involved;
§ 35. Clause (ii) of subparagraph (F) of paragraph 4 of subsection (b)
of section 4322 of the insurance law, as added by chapter 219 of the
laws of 2011, is amended to read as follows:
(ii) immunizations that have in effect a recommendation [from the
advisory committee on immunization practices of the centers for disease
control and prevention] PURSUANT TO NATIONALLY RECOGNIZED CLINICAL PRAC-
TICE GUIDELINES with respect to the individual involved;
§ 36. Clause (iii) of subparagraph (B) paragraph 3 of subsection (j)
of section 7813 of the insurance law, as added by chapter 499 of the
laws of 2009, is amended to read as follows:
(iii) having a level of disability similar to that described in clause
(i) of this subparagraph, as determined by [the United States Secretary
of Health and Human Services] NATIONALLY RECOGNIZED BEST PRACTICES.
§ 37. Paragraph 4 of subdivision (c) of section 36.04 of the mental
hygiene law, as added by section 1 of part HH of chapter 57 of the laws
of 2023, is amended to read as follows:
(4) where executed, agreements establishing formal relationships with
designated collaborating organizations to provide certain certified
community behavioral health clinic services[, consistent with guidance
issued by the United States department of health and human services
substance abuse and mental health services administration and the office
of mental health and the office of addiction services and supports];
§ 38. Subdivision (a) of section 418 of the family court act, as
amended by chapter 214 of the laws of 1998, is amended to read as
follows:
(a) The court, on its own motion or motion of any party, when paterni-
ty is contested, shall order the mother, the child and the alleged
A. 9077 12
father to submit to one or more genetic marker or DNA marker tests of a
type generally acknowledged as reliable by an accreditation body [desig-
nated by the secretary of the federal department of health and human
services] and performed by a laboratory approved by such an accredi-
tation body and by the commissioner of health or by a duly qualified
physician to aid in the determination of whether the alleged father is
or is not the father of the child. No such test shall be ordered, howev-
er, upon a written finding by the court that it is not in the best
interests of the child on the basis of res judicata, equitable estoppel
or the presumption of legitimacy of a child born to a married woman. The
record or report of the results of any such genetic marker or DNA test
shall be received in evidence, pursuant to subdivision (e) of rule
forty-five hundred eighteen of the civil practice law and rules where no
timely objection in writing has been made thereto. Any order pursuant to
this section shall state in plain language that the results of such test
shall be admitted into evidence, pursuant to rule forty-five hundred
eighteen of the civil practice law and rules absent timely objections
thereto and that if such timely objections are not made, they shall be
deemed waived and shall not be heard by the court. If the record or
report of results of any such genetic marker or DNA test or tests indi-
cate at least a ninety-five percent probability of paternity, the admis-
sion of such record or report shall create a rebuttable presumption of
paternity, and, if unrebutted, shall establish the paternity of and
liability for the support of a child pursuant to this article and arti-
cle five of this act.
§ 39. Subdivision (a) of section 532 of the family court act, as
amended by chapter 214 of the laws of 1998, is amended to read as
follows:
(a) The court shall advise the parties of their right to one or more
genetic marker tests or DNA tests and, on the court's own motion or the
motion of any party, shall order the mother, her child and the alleged
father to submit to one or more genetic marker or DNA tests of a type
generally acknowledged as reliable by an accreditation body [designated
by the secretary of the federal department of health and human services]
and performed by a laboratory approved by such an accreditation body and
by the commissioner of health or by a duly qualified physician to aid in
the determination of whether the alleged father is or is not the father
of the child. No such test shall be ordered, however, upon a written
finding by the court that it is not in the best interests of the child
on the basis of res judicata, equitable estoppel, or the presumption of
legitimacy of a child born to a married woman. The record or report of
the results of any such genetic marker or DNA test ordered pursuant to
this section or pursuant to section one hundred eleven-k of the social
services law shall be received in evidence by the court pursuant to
subdivision (e) of rule forty-five hundred eighteen of the civil prac-
tice law and rules where no timely objection in writing has been made
thereto and that if such timely objections are not made, they shall be
deemed waived and shall not be heard by the court. If the record or
report of the results of any such genetic marker or DNA test or tests
indicate at least a ninety-five percent probability of paternity, the
admission of such record or report shall create a rebuttable presumption
of paternity, and shall establish, if unrebutted, the paternity of and
liability for the support of a child pursuant to this article and arti-
cle four of this act.
A. 9077 13
§ 40. Paragraph (iv) of subdivision (d-1) of section 756-a of the
family court act, as amended by section 14-a of part K of chapter 56 of
the laws of 2019, is amended to read as follows:
(iv) whether and when the child: (A) will be returned to the parent;
(B) should be placed for adoption with the social services official
filing a petition for termination of parental rights; (C) should be
referred for legal guardianship; (D) should be placed permanently with a
fit and willing relative; or (E) should be placed in another planned
permanent living arrangement with a significant connection to an adult
willing to be a permanency resource for the child if the child is age
sixteen or older and (1) the social services official has documented to
the court: (I) intensive, ongoing, and, as of the date of the hearing,
unsuccessful efforts made by the social services district to return the
child home or secure a placement for the child with a fit and willing
relative including adult siblings, a legal guardian, or an adoptive
parent, including through efforts that utilize search technology includ-
ing social media to find biological family members for children, (II)
the steps the social services district is taking to ensure that (A) the
child's foster family home or child care facility is following the
reasonable and prudent parent standard in accordance with [guidance
provided by the United States department of health and human services]
NATIONALLY RECOGNIZED BEST PRACTICES, and (B) the child has regular,
ongoing opportunities to engage in age or developmentally appropriate
activities including by consulting with the child in an age-appropriate
manner about the opportunities of the child to participate in activ-
ities; and (2) the social services district has documented to the court
and the court has determined that there are compelling reasons for
determining that it continues to not be in the best interest of the
child to return home, be referred for termination of parental rights and
placed for adoption, placed with a fit and willing relative, or placed
with a legal guardian; and (3) the court has made a determination
explaining why, as of the date of the hearing, another planned living
arrangement with a significant connection to an adult willing to be a
permanency resource for the child is the best permanency plan for the
child; and
§ 41. Subdivisions 4 and 6 of section 11-c of the volunteer ambulance
workers' benefit law, as added by chapter 603 of the laws of 2006, are
amended to read as follows:
4. For the purposes of this section, the term "significant risk of
transmission" means the alleged conduct or actions taken by a victim or
patient or any other action, situation or event that occurs while a
volunteer ambulance worker is performing services in the line of duty
that has created a recognized and significant risk of infection of a
volunteer ambulance worker with the human immunodeficiency virus (HIV),
as determined by the commissioner of health, consistent with NATIONALLY
RECOGNIZED CLINICAL PRACTICE guidelines, protocols, and findings [of the
United States centers for disease control and prevention].
6. The commissioner of health shall issue guidelines to facilitate the
identification of circumstances potentially exposing a volunteer ambu-
lance worker to a significant risk of transmission of the human immuno-
deficiency virus (HIV). Such guidelines shall be consistent with
NATIONALLY RECOGNIZED CLINICAL PRACTICE criteria [accepted by the feder-
al centers for disease control and prevention]. Such guidelines shall
also provide information regarding related counseling and testing proce-
dures available to such individuals.
A. 9077 14
§ 42. Subdivisions 4 and 6 of section 11-c of the volunteer firefight-
ers' benefit law, as added by chapter 603 of the laws of 2006, are
amended to read as follows:
4. For the purposes of this section, the term "significant risk of
transmission" means the alleged conduct or actions taken by a victim or
patient or any other action, situation or event that occurs while a
volunteer firefighter is performing services in the line of duty that
has created a recognized and significant risk of infection of a volun-
teer firefighter with the human immunodeficiency virus (HIV), as deter-
mined by the commissioner of health, consistent with NATIONALLY RECOG-
NIZED CLINICAL PRACTICE guidelines, protocols, and findings [of the
United States centers for disease control and prevention].
6. The commissioner of health shall issue guidelines to facilitate the
identification of circumstances potentially exposing a volunteer fire-
fighter to a significant risk of transmission of the human immunodefici-
ency virus (HIV). Such guidelines shall be consistent with NATIONALLY
RECOGNIZED CLINICAL PRACTICE criteria [accepted by the federal centers
for disease control and prevention]. Such guidelines shall also provide
information regarding related counseling and testing procedures avail-
able to such individuals.
§ 43. Subdivision 1 of section 169 of the workers' compensation law,
as added by chapter 559 of the laws of 2022, is amended to read as
follows:
1. The board shall accept the certifications [of the Centers for
Disease Control and Prevention World Trade Center Health Program] AS
DETERMINED BY THE COMMISSIONER OF HEALTH as presumptive evidence of
causation of certified illnesses pursuant to 42 USC 300mm for claims
filed for conditions of impairment of health or death pursuant to a
qualifying condition.
§ 44. This act shall take effect immediately.