Updating the HRSA-Supported Women's Preventive Services Guidelines, 95148-95150 [2016-31129]

Download as PDF 95148 Federal Register / Vol. 81, No. 248 / Tuesday, December 27, 2016 / Notices Abstract: Currently HRSA is cleared to use the National Institutes of Health’s (NIH) Biographical Sketch and Public Health Service (PHS) Inclusion Enrollment forms (0925–0001) for HRSA’s SF424 Research & Related (R&R) application package research grants. However, both of these documents contain NIH-specific references. To use the forms, HRSA plans to remove the NIH-specific references and obtain its own OMB control number for the collection of this information. The current Statement of Appointment (form PHS–2271) is also tailored to NIH programs. HRSA plans to remove references to NIH and where appropriate replace them with references to HRSA for use in the SF424 R&R application package. Need and Proposed Use of the Information: Currently, there are two Bureaus within HRSA, the Maternal and Child Health Bureau (MCHB) and the Bureau of Health Workforce (BHW), that use the Biographical Sketch. In addition to the Biographical Sketch, MCHB also uses the PHS Inclusion Enrollment form, and BHW uses the Statement of Appointment form as required elements of the SF424 Research & Related application package. These Bureaus plan to modify these forms in slightly different ways to meet the needs of their own research and training grant programs. In MCHB’s research grant programs, the modified Biographical Sketch form will be used by applicants to summarize the qualifications of key personnel on their proposed research team; the grant reviewers will use this information to assess the capabilities of the research team to carry out the research project. MCHB’s modified PHS Inclusion Enrollment form will be used by applicants to summarize their expected population of research study participants at the time of submission of their proposal; it will also be used for Enrollment Reporting during the annual Noncompeting Continuation Award. Monitoring Inclusion Enrollment is one important component of ensuring statistically meaningful demographics (race, ethnicity, and gender) among research study participants in MCHB’s research grant portfolio. MCHB does not use the Statement of Appointment form, as it does not pertain to the MCHB research program. Similarly, in BHW the modified Biographical Sketch form will be used by applicants to summarize the qualifications of key personnel proposed as project staff; the grant reviewers will use this information to assess the capabilities of the applicant organization to carry out the proposed project. The modified Statement of Appointment form is used to document the appointment of individuals supported by the award to applicable institutional research and training programs. BHW does not use the PHS Inclusion Enrollment form, as it does not pertain to the BHW training and research programs. Likely Respondents: Respondents are applicants to HRSA’s research programs in MCHB and research and training programs in BHW. Burden Statement: Burden in this context means the time expended by persons to generate, maintain, retain, disclose or provide the information requested. This includes the time needed to review instructions; to develop, acquire, install, and utilize technology and systems for the purpose of collecting, validating and verifying information, processing and maintaining information, and disclosing and providing information; to train personnel and be able to respond to a collection of information; to search data sources; to complete and review the collection of information; and to transmit or otherwise disclose the information. The total annual burden hours estimated for this Information Collection Request are summarized in the table below. TOTAL ESTIMATED ANNUALIZED BURDEN HOURS Number of respondents Form name Total .............................................................................. asabaliauskas on DSK3SPTVN1PROD with NOTICES Biographical Sketch for MCHB research grant applicants .. PHS Inclusion Enrollment form for MCHB research grant applications ....................................................................... Biographical Sketch for BHW training and research grant applicants ......................................................................... Statement of Appointment form for BHW training grantees HRSA specifically requests comments on (1) the necessity and utility of the proposed information collection for the proper performance of the agency’s functions; (2) the accuracy of the estimated burden; (3) ways to enhance the quality, utility, and clarity of the information to be collected; and (4) the use of automated collection techniques or other forms of information technology to minimize the information collection burden. Jason E. Bennett, Director, Division of the Executive Secretariat. [FR Doc. 2016–31080 Filed 12–23–16; 8:45 am] BILLING CODE 4165–15–P VerDate Sep<11>2014 20:45 Dec 23, 2016 Jkt 241001 Number of responses per respondent Total burden hours 5 1000 2 2000 200 1 200 .5 100 1000 800 5 7 5000 5600 2 .5 10,000 2,800 2200 ........................ 11,800 ........................ 14,900 Health Resources and Services Administration Updating the HRSA-Supported Women’s Preventive Services Guidelines Health Resources and Services Administration, HHS. ACTION: Notice. AGENCY: Effective December 20, 2016, the Health Resources and Services Administration (HRSA) updated the HRSA-supported Women’s Preventive SUMMARY: Frm 00051 Average burden per response (in hours) 200 DEPARTMENT OF HEALTH AND HUMAN SERVICES PO 00000 Total responses Fmt 4703 Sfmt 4703 Services Guidelines for purposes of health insurance coverage for preventive services that address health needs specific to women based on clinical recommendations from the Women’s Preventive Services Initiative. This notice serves as an announcement of the decision to update the guidelines as listed below. Please see https:// www.hrsa.gov/womensguidelines2016 for additional information. FOR FURTHER INFORMATION CONTACT: HRSA, Maternal and Child Health Bureau at email: wellwomancare@ hrsa.gov. SUPPLEMENTARY INFORMATION: E:\FR\FM\27DEN1.SGM 27DEN1 Federal Register / Vol. 81, No. 248 / Tuesday, December 27, 2016 / Notices Breast Cancer Screening for AverageRisk Women The Women’s Preventive Services Initiative recommends that average-risk women initiate mammography screening no earlier than age 40 and no later than age 50. Screening mammography should occur at least biennially and as frequently as annually. Screening should continue through at least age 74 and age alone should not be the basis to discontinue screening. These screening recommendations are for women at average risk of breast cancer. Women at increased risk should also undergo periodic mammography screening, however, recommendations for additional services are beyond the scope of this recommendation. Breastfeeding Services and Supplies The Women’s Preventive Services Initiative recommends comprehensive lactation support services (including counseling, education, and breastfeeding equipment and supplies) during the antenatal, perinatal, and postpartum periods to ensure the successful initiation and maintenance of breastfeeding. asabaliauskas on DSK3SPTVN1PROD with NOTICES Screening for Cervical Cancer The Women’s Preventive Services Initiative recommends cervical cancer screening for average-risk women aged 21 to 65 years. For women aged 21 to 29 years, the Women’s Preventive Services Initiative recommends cervical cancer screening using cervical cytology (Pap test) every 3 years. Cotesting with cytology and human papillomavirus testing is not recommended for women younger than 30 years. Women aged 30 to 65 years should be screened with cytology and human papillomavirus testing every 5 years or cytology alone every 3 years. Women who are at average risk should not be screened more than once every 3 years. Contraception The Women’s Preventive Services Initiative recommends that adolescent and adult women have access to the full range of female-controlled contraceptives to prevent unintended pregnancy and improve birth outcomes. Contraceptive care should include contraceptive counseling, initiation of contraceptive use, and follow-up care (e.g., management, and evaluation as well as changes to and removal or discontinuation of the contraceptive method). The Women’s Preventive Services Initiative recommends that the full range of female-controlled U.S. Food and Drug Administrationapproved contraceptive methods, VerDate Sep<11>2014 20:45 Dec 23, 2016 Jkt 241001 95149 effective family planning practices, and sterilization procedures be available as part of contraceptive care. The full range of contraceptive methods for women currently identified by the U.S. Food and Drug Administration include: (1) Sterilization surgery for women, (2) surgical sterilization via implant for women, (3) implantable rods, (4) copper intrauterine devices, (5) intrauterine devices with progestin (all durations and doses), (6) the shot or injection, (7) oral contraceptives (combined pill), 8) oral contraceptives (progestin only, and), (9) oral contraceptives (extended or continuous use), (10) the contraceptive patch, (11) vaginal contraceptive rings, (12) diaphragms, (13) contraceptive sponges, (14) cervical caps, (15) female condoms, (16) spermicides, and (17) emergency contraception (levonorgestrel), and (18) emergency contraception (ulipristal acetate), and additional methods as identified by the FDA. Additionally, instruction in fertility awareness-based methods, including the lactation amenorrhea method, although less effective, should be provided for women desiring an alternative method. and women with an increased risk of HIV infection. Screening for HIV is recommended for all pregnant women upon initiation of prenatal care with retesting during pregnancy based on risk factors. Rapid HIV testing is recommended for pregnant women who present in active labor with an undocumented HIV status. Screening during pregnancy enables prevention of vertical transmission. Screening for Gestational Diabetes Mellitus Screening for Human Immunodeficiency Virus Infection Counseling for Sexually Transmitted Infections The Women’s Preventive Services Initiative recommends directed behavioral counseling by a health care provider or other appropriately trained individual for sexually active adolescent and adult women at an increased risk for sexually transmitted infections (STIs). The Women’s Preventive Services Initiative recommends that health care providers use a woman’s sexual history and risk factors to help identify those at an increased risk of STIs. Risk factors may include age younger than 25, a recent history of an STI, a new sex partner, multiple partners, a partner with concurrent partners, a partner with an STI, and a lack of or inconsistent condom use. For adolescents and women not identified as high risk, counseling to reduce the risk of STIs should be considered, as determined by clinical judgement. The Women’s Preventive Services Initiative recommends prevention education and risk assessment for human immunodeficiency virus (HIV) infection in adolescents and women at least annually throughout the lifespan. All women should be tested for HIV at least once during their lifetime. Additional screening should be based on risk, and screening annually or more often may be appropriate for adolescents Well-Woman Preventive Visits The Women’s Preventive Services Initiative recommends that women receive at least one preventive care visit per year beginning in adolescence and continuing across the lifespan to ensure that the recommended preventive services including preconception, and many services necessary for prenatal and interconception care are obtained. The primary purpose of these visits The Women’s Preventive Services Initiative recommends screening pregnant women for gestational diabetes mellitus after 24 weeks of gestation (preferably between 24 and 28 weeks of gestation) in order to prevent adverse birth outcomes. Screening with a 50-g oral glucose challenge test (followed by a 3-hour 100-g oral glucose tolerance test if results on the initial oral glucose challenge test are abnormal) is preferred because of its high sensitivity and specificity. The Women’s Preventive Services Initiative suggests that women with risk factors for diabetes mellitus be screened for preexisting diabetes before 24 weeks of gestation—ideally at the first prenatal visit, based on current clinical best practices. PO 00000 Frm 00052 Fmt 4703 Sfmt 4703 Screening for Interpersonal and Domestic Violence The Women’s Preventive Services Initiative recommends screening adolescents and women for interpersonal and domestic violence, at least annually, and, when needed, providing or referring for initial intervention services. Interpersonal and domestic violence includes physical violence, sexual violence, stalking and psychological aggression (including coercion), reproductive coercion, neglect, and the threat of violence, abuse, or both. Intervention services include, but are not limited to, counseling, education, harm reduction strategies, and referral to appropriate supportive services. E:\FR\FM\27DEN1.SGM 27DEN1 asabaliauskas on DSK3SPTVN1PROD with NOTICES 95150 Federal Register / Vol. 81, No. 248 / Tuesday, December 27, 2016 / Notices should be the delivery and coordination of recommended preventive services as determined by age and risk factors. The HRSA-supported Women’s Preventive Services Guidelines were originally established in 2011 based on recommendations from a Department of Health and Human Services’ commissioned study by the Institute of Medicine (IOM), now known as the National Academy of Medicine (NAM). Since then, there have been advancements in science and gaps identified in the existing guidelines, including a greater emphasis on practice-based clinical considerations. To address these, HRSA awarded a 5year cooperative agreement in March 2016 to convene a coalition of clinician, academic, and consumer-focused health professional organizations and conduct a scientifically rigorous review to develop recommendations for updated Women’s Preventive Services Guidelines in accordance with the model created by the NAM Clinical Practice Guidelines We Can Trust. The American College of Obstetricians and Gynecologists was awarded the cooperative agreement and formed an expert panel called the Women’s Preventive Services Initiative. Under section 2713 of the Public Health Service Act, non-grandfathered group health plans and issuers of nongrandfathered group and individual health insurance coverage are required to cover specified preventive services without a copayment, coinsurance, deductible, or other cost sharing, including preventive care and screenings for women as provided for in comprehensive guidelines supported by HRSA for this purpose. Nongrandfathered plans and coverage (generally, plans or policies created or sold after March 23, 2010, or older plans or policies that have been changed in certain ways since that date) are required to provide coverage without cost sharing consistent with these guidelines beginning with the first plan year (in the individual market, policy year) that begins on or after December 20, 2017. The guidelines concerning contraceptive methods and counseling do not apply to women who are participants or beneficiaries in group health plans sponsored by religious employers. Effective August 1, 2013, a religious employer is defined as an employer that is organized and operates as a non-profit entity and is referred to in section 6033(a)(3)(A)(i) or (iii) of the Internal Revenue Code. HRSA notes that, as of August 1, 2013, group health plans established or maintained by religious employers (and group health VerDate Sep<11>2014 20:45 Dec 23, 2016 Jkt 241001 insurance coverage provided in connection with such plans) are exempt from the requirement to cover contraceptive services under section 2713 of the Public Health Service Act, as incorporated into the Employee Retirement Income Security Act and the Internal Revenue Code. HRSA also notes that, as of January 1, 2014, accommodations are available to group health plans established or maintained by certain eligible organizations (and group health insurance coverage provided in connection with such plans), as well as student health insurance coverage arranged by eligible organizations, with respect to the contraceptive coverage requirement. See Coverage of Certain Preventive Services Under the Affordable Care Act (78 FR 39870, July 2, 2013). James Macrae, Acting Administrator. [FR Doc. 2016–31129 Filed 12–23–16; 8:45 am] BILLING CODE 4165–15–P DEPARTMENT OF HEALTH AND HUMAN SERVICES Office of Inspector General Announcement of Updated Requirements and Registration for ‘‘The Simple Extensible Sampling Tool Challenge’’ Office of Inspector General (OIG), HHS. AGENCY: ACTION: Notice. On September 29, 2016, OIG announced ‘‘The Simple Extensible Sampling Tool Challenge’’. This notice serves as an update to the original notice which stated that upon receipt of an updated submission the previous submission would be excluded in its entirety from the competition. This updated notice removes this restriction for entries from teams that have been previously identified as finalists. Any finalist may update their entry without losing their finalist designation. Updates from the finalists will be accepted until 5:00 p.m. EST on the fourteenth day after the fifth finalist has been identified or May 15, 2017, 5:00 p.m. EST, whichever comes first. The newest entry from each team will be used for all judging purposes unless otherwise requested by the team. Other than the above change, all rules and requirements outlined in the September 29, 2016, Federal Register notice remain in effect. SUMMARY: PO 00000 Frm 00053 Fmt 4703 Sfmt 4703 Dated: December 21, 2016. Daniel R. Levinson, Inspector General. [FR Doc. 2016–31182 Filed 12–23–16; 8:45 am] BILLING CODE 4152–01–P DEPARTMENT OF HEALTH AND HUMAN SERVICES National Institutes of Health Office of the Director, National Institutes of Health; Notice of Meeting Pursuant to section 10(d) of the Federal Advisory Committee Act, as amended (5 U.S.C. Appendix 2), notice is hereby given of the meeting of the Council of Councils. The meeting will be open to the public as indicated below, with attendance limited to space available. Individuals who plan to attend and need special assistance, such as sign language interpretation or other reasonable accommodations, should notify the Contact Person listed below in advance of the meeting. The open session will be videocast and can be accessed from the NIH Videocasting and Podcasting Web site (https:// videocast.nih.gov). A portion of the meeting will be closed to the public in accordance with the provisions set forth in sections 552b(c)(4), and 552b(c)(6), Title 5 U.S.C., as amended. The grant applications and the discussions could disclose confidential trade secrets or commercial property such as patentable material, and personal information concerning individuals associated with the grant applications, the disclosure of which would constitute a clearly unwarranted invasion of personal privacy. Name of Committee: Council of Councils. Open: January 27, 2017. Time: 8:15 a.m. to 11:30 a.m. Agenda: Call to Order and Introductions; Announcements and Updates; Tracking Utility of Common Fund Data Sets; Small Molecules from the Human Microbiota; Invited Speaker; NIH Update; Discussion; 2017 Biennial Advisory Council Report— Compliance with the NIH Policy on the Inclusion of Women and Minorities in Clinical Research. Place: National Institutes of Health, 9000 Rockville Pike, Building 31, C Wing, 6th Floor, Conference Room 10, Bethesda, MD 20892. Closed: January 27, 2017. Time: 12:00 p.m. to 1:00 p.m. Agenda: Review of grant applications. Place: National Institutes of Health, 9000 Rockville Pike, Building 31, C Wing, 6th Floor, Conference Room 10, Bethesda, MD 20892. Open: January 27, 2017. E:\FR\FM\27DEN1.SGM 27DEN1

Agencies

[Federal Register Volume 81, Number 248 (Tuesday, December 27, 2016)]
[Notices]
[Pages 95148-95150]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2016-31129]


-----------------------------------------------------------------------

DEPARTMENT OF HEALTH AND HUMAN SERVICES

Health Resources and Services Administration


Updating the HRSA-Supported Women's Preventive Services 
Guidelines

AGENCY: Health Resources and Services Administration, HHS.

ACTION: Notice.

-----------------------------------------------------------------------

SUMMARY: Effective December 20, 2016, the Health Resources and Services 
Administration (HRSA) updated the HRSA-supported Women's Preventive 
Services Guidelines for purposes of health insurance coverage for 
preventive services that address health needs specific to women based 
on clinical recommendations from the Women's Preventive Services 
Initiative. This notice serves as an announcement of the decision to 
update the guidelines as listed below. Please see https://www.hrsa.gov/womensguidelines2016 for additional information.

FOR FURTHER INFORMATION CONTACT: HRSA, Maternal and Child Health Bureau 
at email: wellwomancare@hrsa.gov.

SUPPLEMENTARY INFORMATION:

[[Page 95149]]

Breast Cancer Screening for Average-Risk Women

    The Women's Preventive Services Initiative recommends that average-
risk women initiate mammography screening no earlier than age 40 and no 
later than age 50. Screening mammography should occur at least 
biennially and as frequently as annually. Screening should continue 
through at least age 74 and age alone should not be the basis to 
discontinue screening.
    These screening recommendations are for women at average risk of 
breast cancer. Women at increased risk should also undergo periodic 
mammography screening, however, recommendations for additional services 
are beyond the scope of this recommendation.

Breastfeeding Services and Supplies

    The Women's Preventive Services Initiative recommends comprehensive 
lactation support services (including counseling, education, and 
breastfeeding equipment and supplies) during the antenatal, perinatal, 
and postpartum periods to ensure the successful initiation and 
maintenance of breastfeeding.

Screening for Cervical Cancer

    The Women's Preventive Services Initiative recommends cervical 
cancer screening for average-risk women aged 21 to 65 years. For women 
aged 21 to 29 years, the Women's Preventive Services Initiative 
recommends cervical cancer screening using cervical cytology (Pap test) 
every 3 years. Cotesting with cytology and human papillomavirus testing 
is not recommended for women younger than 30 years. Women aged 30 to 65 
years should be screened with cytology and human papillomavirus testing 
every 5 years or cytology alone every 3 years. Women who are at average 
risk should not be screened more than once every 3 years.

Contraception

    The Women's Preventive Services Initiative recommends that 
adolescent and adult women have access to the full range of female-
controlled contraceptives to prevent unintended pregnancy and improve 
birth outcomes. Contraceptive care should include contraceptive 
counseling, initiation of contraceptive use, and follow-up care (e.g., 
management, and evaluation as well as changes to and removal or 
discontinuation of the contraceptive method). The Women's Preventive 
Services Initiative recommends that the full range of female-controlled 
U.S. Food and Drug Administration-approved contraceptive methods, 
effective family planning practices, and sterilization procedures be 
available as part of contraceptive care.
    The full range of contraceptive methods for women currently 
identified by the U.S. Food and Drug Administration include: (1) 
Sterilization surgery for women, (2) surgical sterilization via implant 
for women, (3) implantable rods, (4) copper intrauterine devices, (5) 
intrauterine devices with progestin (all durations and doses), (6) the 
shot or injection, (7) oral contraceptives (combined pill), 8) oral 
contraceptives (progestin only, and), (9) oral contraceptives (extended 
or continuous use), (10) the contraceptive patch, (11) vaginal 
contraceptive rings, (12) diaphragms, (13) contraceptive sponges, (14) 
cervical caps, (15) female condoms, (16) spermicides, and (17) 
emergency contraception (levonorgestrel), and (18) emergency 
contraception (ulipristal acetate), and additional methods as 
identified by the FDA. Additionally, instruction in fertility 
awareness-based methods, including the lactation amenorrhea method, 
although less effective, should be provided for women desiring an 
alternative method.

Screening for Gestational Diabetes Mellitus

    The Women's Preventive Services Initiative recommends screening 
pregnant women for gestational diabetes mellitus after 24 weeks of 
gestation (preferably between 24 and 28 weeks of gestation) in order to 
prevent adverse birth outcomes. Screening with a 50-g oral glucose 
challenge test (followed by a 3-hour 100-g oral glucose tolerance test 
if results on the initial oral glucose challenge test are abnormal) is 
preferred because of its high sensitivity and specificity.
    The Women's Preventive Services Initiative suggests that women with 
risk factors for diabetes mellitus be screened for preexisting diabetes 
before 24 weeks of gestation--ideally at the first prenatal visit, 
based on current clinical best practices.

Screening for Human Immunodeficiency Virus Infection

    The Women's Preventive Services Initiative recommends prevention 
education and risk assessment for human immunodeficiency virus (HIV) 
infection in adolescents and women at least annually throughout the 
lifespan. All women should be tested for HIV at least once during their 
lifetime. Additional screening should be based on risk, and screening 
annually or more often may be appropriate for adolescents and women 
with an increased risk of HIV infection.
    Screening for HIV is recommended for all pregnant women upon 
initiation of prenatal care with retesting during pregnancy based on 
risk factors. Rapid HIV testing is recommended for pregnant women who 
present in active labor with an undocumented HIV status. Screening 
during pregnancy enables prevention of vertical transmission.

Screening for Interpersonal and Domestic Violence

    The Women's Preventive Services Initiative recommends screening 
adolescents and women for interpersonal and domestic violence, at least 
annually, and, when needed, providing or referring for initial 
intervention services. Interpersonal and domestic violence includes 
physical violence, sexual violence, stalking and psychological 
aggression (including coercion), reproductive coercion, neglect, and 
the threat of violence, abuse, or both. Intervention services include, 
but are not limited to, counseling, education, harm reduction 
strategies, and referral to appropriate supportive services.

Counseling for Sexually Transmitted Infections

    The Women's Preventive Services Initiative recommends directed 
behavioral counseling by a health care provider or other appropriately 
trained individual for sexually active adolescent and adult women at an 
increased risk for sexually transmitted infections (STIs).
    The Women's Preventive Services Initiative recommends that health 
care providers use a woman's sexual history and risk factors to help 
identify those at an increased risk of STIs. Risk factors may include 
age younger than 25, a recent history of an STI, a new sex partner, 
multiple partners, a partner with concurrent partners, a partner with 
an STI, and a lack of or inconsistent condom use. For adolescents and 
women not identified as high risk, counseling to reduce the risk of 
STIs should be considered, as determined by clinical judgement.

Well-Woman Preventive Visits

    The Women's Preventive Services Initiative recommends that women 
receive at least one preventive care visit per year beginning in 
adolescence and continuing across the lifespan to ensure that the 
recommended preventive services including preconception, and many 
services necessary for prenatal and interconception care are obtained. 
The primary purpose of these visits

[[Page 95150]]

should be the delivery and coordination of recommended preventive 
services as determined by age and risk factors.
    The HRSA-supported Women's Preventive Services Guidelines were 
originally established in 2011 based on recommendations from a 
Department of Health and Human Services' commissioned study by the 
Institute of Medicine (IOM), now known as the National Academy of 
Medicine (NAM). Since then, there have been advancements in science and 
gaps identified in the existing guidelines, including a greater 
emphasis on practice-based clinical considerations. To address these, 
HRSA awarded a 5-year cooperative agreement in March 2016 to convene a 
coalition of clinician, academic, and consumer-focused health 
professional organizations and conduct a scientifically rigorous review 
to develop recommendations for updated Women's Preventive Services 
Guidelines in accordance with the model created by the NAM Clinical 
Practice Guidelines We Can Trust. The American College of Obstetricians 
and Gynecologists was awarded the cooperative agreement and formed an 
expert panel called the Women's Preventive Services Initiative.
    Under section 2713 of the Public Health Service Act, non-
grandfathered group health plans and issuers of non-grandfathered group 
and individual health insurance coverage are required to cover 
specified preventive services without a copayment, coinsurance, 
deductible, or other cost sharing, including preventive care and 
screenings for women as provided for in comprehensive guidelines 
supported by HRSA for this purpose. Non-grandfathered plans and 
coverage (generally, plans or policies created or sold after March 23, 
2010, or older plans or policies that have been changed in certain ways 
since that date) are required to provide coverage without cost sharing 
consistent with these guidelines beginning with the first plan year (in 
the individual market, policy year) that begins on or after December 
20, 2017.
    The guidelines concerning contraceptive methods and counseling do 
not apply to women who are participants or beneficiaries in group 
health plans sponsored by religious employers. Effective August 1, 
2013, a religious employer is defined as an employer that is organized 
and operates as a non-profit entity and is referred to in section 
6033(a)(3)(A)(i) or (iii) of the Internal Revenue Code. HRSA notes 
that, as of August 1, 2013, group health plans established or 
maintained by religious employers (and group health insurance coverage 
provided in connection with such plans) are exempt from the requirement 
to cover contraceptive services under section 2713 of the Public Health 
Service Act, as incorporated into the Employee Retirement Income 
Security Act and the Internal Revenue Code. HRSA also notes that, as of 
January 1, 2014, accommodations are available to group health plans 
established or maintained by certain eligible organizations (and group 
health insurance coverage provided in connection with such plans), as 
well as student health insurance coverage arranged by eligible 
organizations, with respect to the contraceptive coverage requirement. 
See Coverage of Certain Preventive Services Under the Affordable Care 
Act (78 FR 39870, July 2, 2013).

James Macrae,
Acting Administrator.
[FR Doc. 2016-31129 Filed 12-23-16; 8:45 am]
 BILLING CODE 4165-15-P
This site is protected by reCAPTCHA and the Google Privacy Policy and Terms of Service apply.