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701 records in US in 2017
United States · United States Congress · 1 May 2017
Medicaid and CHIP Territory Transparency and Information Act This bill requires the Centers for Medicare & Medicaid Services to publish on its website, and periodically update, specified information related to federal expenditures under Medicaid and the Children's Health Insurance Program (CHIP) in each of the U.S. territories.
United States · United States Congress · 1 May 2017
Expresses support for the designation of Health and Fitness Month and for efforts to educate Americans on the importance of a healthy and nutritious lifestyle.
United States · United States Congress · 1 May 2017
Supports the designation of National Bartter Syndrome Day. (Bartter syndrome is caused by genetic defects that affect kidney function. Symptoms include muscle weakness and growth delay.)
United States · United States Congress · 28 April 2017
Patient Experience in Research Act of 2017 This bill requires the Food and Drug Administration to carry out a pilot project under which sponsors of new drugs or biological products agree to evaluate: (1) the distress experienced by patients in clinical trials for medications intended to treat a serious condition, and (2) the effects of providing support to distressed patients on the outcome of a clinical trial. The user fee is waived for new drug applications that include data from such an evaluation.
United States · United States Congress · 28 April 2017
Breaking Addiction Act of 2017 This bill allows state Medicaid programs to provide medical assistance for community-based, inpatient, substance-use-disorder treatment services furnished in facilities with 60 or fewer beds to individuals between 21 and 65 years of age.
United States · United States Congress · 28 April 2017
Repeal of the Obamacare Bay State Boondoogle Act This bill requires that the Medicare hospital wage index floor for non-rural areas be calculated using state-specific, rather than national, budget neutrality. (The Medicare hospital wage index is used to calculate geographic adjustments to Medicare reimbursements.)
United States · United States Congress · 28 April 2017
Expresses support for the designation of National Congenital Diaphragmatic Hernia Awareness Month. (Congenital diaphragmatic hernia is a birth defect that occurs when the diaphragm fails to fully form, allowing abdominal organs to migrate into the chest cavity and preventing lung growth.) Encourages that steps should be taken to: raise awareness of and increase public knowledge about congenital diaphragmatic hernia (CDH); inform people about the dangers of CDH; disseminate information on the importance of quality neonatal care for CDH patients; promote quality prenatal care and the use of ultrasounds to detect CDH in utero; and support research funding of CDH to improve screening and treatment, discover its causes, and develop a cure.
United States · United States Congress · 28 April 2017
Chiropractic Care Available to All Veterans Act This bill amends the Department of Veterans Affairs Health Care Programs Enhancement Act of 2001 to require a program under which the Secretary of Veterans Affairs provides chiropractic care and services to veterans through Department of Veterans Affairs (VA) medical centers and clinics to be carried out at: (1) no fewer than 75 medical centers by December 31, 2014, and (2) all medical centers by December 31, 2018. Chiropractic examinations and services are included within required VA medical, rehabilitative, and preventive health care services.
United States · United States Congress · 28 April 2017
Ensuring Children’s Access to Specialty Care Act of 2017 This bill amends the Public Health Service Act to include pediatric subspecialties in primary health services for purposes of the National Health Service Corps (NHSC). Psychiatrists who are pediatric subspecialists are included in behavioral and mental health professionals. (These amendments make pediatric subspecialists, including psychiatrists, eligible for the NHSC fellowship program for the delivery of primary health services in health professional shortage areas, the NHSC Scholarship Program, and the NHSC Loan Repayment Program.) “Health professional shortage area” can mean an underserved population of children and adolescents.
United States · United States Congress · 27 April 2017
This bill expands the list of individuals to whom a whistleblower may disclose information evidencing a violation of law, gross mismanagement, waste of funds, abuse of authority, or danger to public health or safety to include such whistleblower's immediate supervisor or agency head, the Director of National Intelligence, the Inspector General of the Intelligence Community, or an employee designated to receive such disclosures.
United States · United States Congress · 27 April 2017
Creating and Restoring Equal Access To Equivalent Samples Act of 2017 or the CREATES Act of 2017 This bill permits the developer of a drug or biological product to bring a civil action against the license holder of an approved drug or biological product if the holder has declined to make available sufficient quantities of the approved drug or product for the developer's testing.
United States · United States Congress · 27 April 2017
This bill amends the Public Health Service Act, if the American Health Care Act (H.R. 1628) is enacted, to make plans made available by the federal government to Members of Congress and congressional staff subject to state waivers of the Patient Protection and Affordable Care Act (PPACA) requirement for health insurance to cover the essential health benefits and PPACA restrictions on premium variation by age and health status.
United States · United States Congress · 27 April 2017
Trade Protection Not Troll Protection Act This bill amends the Tariff Act of 1930, with respect to unfair practices in the import trade, to consider an industry in the United States to exist if there is in the United States substantial investment in licensing activities that leads to the adoption and development of articles that incorporate the patent, copyright, trademark, mask work, or design. If the U.S. International Trade Commission (ITC), at the beginning of an investigation of an alleged unfair practice, identifies a domestic industry as the dispositive issue in question, it shall direct the assigned administrative law judge (ALJ) to: expedite fact finding on the domestic industry requirement, and issue an initial determination on this matter within 100 days after the investigation begins. Any initial determination by the assigned ALJ shall stay the investigation pending ITC action. The ITC may determine during an investigation that exclusion of the articles concerned from entry into the United States would not be in the public interest, and terminate the investigation, in whole or in part, without any further determination, after considering the nature of the articles concerned and the effect of exclusion upon: the public health and welfare, the U.S. economy (including competitive conditions), the production of like or directly competitive articles by the complainant and its licensees, and U.S. consumers. Any person adversely affected by an ITC ruling that identifies a domestic industry as the dispositive issue in question may appeal that ruling, within 60 days after all administrative remedies are exhausted, to the U.S. Court of Appeals for the Federal Circuit. ITC discretion not to exclude any articles concerned, even though an importer has violated the ban on unfair competition, is repealed. If the ITC also determines that exclusion would be in the public interest, it shall direct exclusion of the articles. During an investigation, if the ITC determines there is reason to believe that an unfair import practice has occurred, and exclusion of the articles concerned would be in the public interest, the ITC may direct the exclusion the articles concerned, after considering the factors mentioned above. (Currently the ITC may not direct an exclusion until an investigation concludes and it determines, as a result of the investigation, that an unfair import trade practice has occurred.)
United States · United States Congress · 27 April 2017
Creating and Restoring Equal Access To Equivalent Samples Act of 2017 or the CREATES Act of 2017 This bill permits the developer of a drug or biological product to bring a civil action against the license holder of an approved drug or biological product if the holder has declined to make available sufficient quantities of the approved drug or product for the developer's testing.
United States · United States Congress · 27 April 2017
Chiropractic Membership in the Public Health Service Commissioned Corps Act of 2017 This bill amends the Public Health Service Act to make certain doctors of chiropractic (chiropractors) eligible for appointment to the United States Public Health Service Commissioned Corps. To be appointed, a chiropractor must be eligible for licensure in a majority of the states or approved by a body acceptable to the Department of Health and Human Services (HHS). HHS and the Surgeon General must ensure that such chiropractors are trained, equipped, and otherwise prepared to fulfill public health and emergency response service responsibilities in the Commissioned Corps. The President must appoint at least six chiropractors to the commissioned Regular Corps and the Ready Reserve Corps. The Surgeon General must report to Congress on measures taken by the President, Surgeon General, and HHS to carry out this bill.
United States · United States Congress · 27 April 2017
Cigarette Smoking Reduction and Electronic Vapor Alternatives Act of 2017 This bill amends the Federal Food, Drug, and Cosmetic Act to authorize the Food and Drug Administration (FDA) to regulate electronic cigarettes through regulation of e-liquids (solutions used in electronic cigarettes) and personal electronic vaporizers (products that convert e-liquids into inhalable vapor). E-liquids and personal electronic vaporizers are excluded from the definition of tobacco products. The bill sets forth requirements for the sale and manufacturing of e-liquids and personal electronic vaporizers including: (1) prohibiting sales to persons younger than 18, (2) establishing manufacturing standards, and (3) requiring certification of compliance with manufacturing standards. The FDA may prohibit advertising of e-liquids and vaporizers to minors. The Office of E-Liquid and Personal Vaporizer Standards Compliance is created in the FDA's Center for Tobacco Products and Tobacco Harm Reduction. State and local laws on e-liquids and personal electronic vaporizers are preempted by this bill. The FDA shall provide Congress a comparative health risk assessment of tobacco products and other nicotine delivery alternatives and rank them based on morbidity and mortality risk as compared to smoking cigarettes.
United States · United States Congress · 27 April 2017
Encourages schools, communities, and organizations to conduct Every Kid Healthy Week activities. Recognizes the importance of promoting healthy lifestyles and healthy learning environments for all children.
United States · United States Congress · 27 April 2017
Fairness for Our Hospitals Act of 2017 This bill amends title XVIII (Medicare) of the Social Security Act to allow a hospital that meets specified criteria and is located in a state with no rural areas to be considered a Medicare-dependent hospital. The Centers for Medicare & Medicaid Services shall establish and implement a process for reimbursing impacted hospitals for any underpayments resulting from this bill's implementation.
United States · United States Congress · 27 April 2017
Rural Access to Hospice Act of 2017 This bill amends title XVIII (Medicare) of the Social Security Act to allow payment under Medicare for certain services furnished to hospice patients by rural health clinics and federally qualified health centers (FQHCs). With respect to a patient who elects to receive hospice care under Medicare, current law generally limits payment for services that are either duplicative of such care or related to the treatment of the individual's terminal illness. However, current law exempts from this limitation: (1) physicians' services furnished by an attending physician not employed by the hospice program; and (2) services provided or arranged by the hospice program. The bill expands this exemption with regard to rural health clinic and FQHC services. Specifically, the payment limitation shall not apply to such services that: (1) would otherwise be physicians' services if furnished by an individual unaffiliated with a rural health clinic or FQHC; and (2) are either arranged by the hospice program or furnished by an attending physician not employed by the hospice program.
United States · United States Congress · 27 April 2017
Medicare Home Health Flexibility Act of 2017 This bill establishes circumstances under which an occupational therapist may conduct an initial or comprehensive assessment for an individual who is eligible for home health services under Medicare. Specifically, an occupational therapist may conduct the assessment if the physician's referral order does not include skilled nursing care but does include: (1) occupational therapy, and (2) physical therapy or speech language pathology.
United States · United States Congress · 27 April 2017
Newborn Care Improvement Act of 2017 This bill increases from 7 to 14 the number of days that the Department of Veterans Affairs (VA) may furnish health care services, including post-delivery care, to the newborn child of a woman veteran who delivered the child in a VA facility or another facility pursuant to a VA contract for such services.
United States · United States Congress · 27 April 2017
Veterans Access to Care Act This bill amends the Public Health Service Act to automatically designate medical facilities of the Department of Veterans Affairs (VA) as health professional shortage areas. Individuals may not participate in both the VA's Health Professionals Education Assistance Program and the National Health Service Corps scholarship or loan repayment programs. The Department of Health and Human Services, in carrying out the National Health Service Corps Program, must consult with the VA regarding health professional shortage areas that are VA medical facilities.
United States · United States Congress · 27 April 2017
Medicare Ambulance Access, Fraud Prevention, and Reform Act of 201 7 This bill increases payment under Medicare for certain ambulance services and otherwise revises provisions related to coverage of such services.
United States · United States Congress · 27 April 2017
Access to Contraception for Women Servicemembers and Dependents Act of 2017 This bill expands the TRICARE health care program to entitle additional female beneficiaries and dependents to care related to the prevention of pregnancy. (Currently, such care is limited to certain female members of the uniformed service or a reserve component performing active duty or certain servicewomen performing inactive-duty training.) Cost-sharing may not be imposed or collected for such pregnancy prevention care, including for any method of contraception provided through a facility of the uniformed services, the TRICARE retail pharmacy program, or the national mail-order pharmacy program. Such pregnancy prevention care shall include: (1) all methods of contraception approved by the Food and Drug Administration (FDA), (2) contraceptive care, (3) sterilization procedures, and (4) patient education and counseling. The Department of Defense shall establish a uniform standard curriculum to be used in family planning education programs for all men and women members of the Armed Forces. Every military treatment facility, upon request, shall provide emergency contraception, information about FDA-approved methods of emergency contraception, and notification of confidentiality rights to any woman who: (1) states, or is accompanied by another individual who states, that the woman is a victim of sexual assault; or (2) is reasonably believed to be a survivor of sexual assault.
United States · United States Congress · 26 April 2017
Access to Contraception for Women Servicemembers and Dependents Act of 2017 This bill expands the TRICARE health care program to entitle additional female beneficiaries and dependents to care related to the prevention of pregnancy. (Currently, such care is limited to certain female members of the uniformed service or a reserve component performing active duty or certain servicewomen performing inactive-duty training.) Cost-sharing may not be imposed or collected for such pregnancy prevention care, including for any method of contraception provided through a facility of the uniformed services, the TRICARE retail pharmacy program, or the national mail-order pharmacy program. Such pregnancy prevention care shall include: (1) all methods of contraception approved by the Food and Drug Administration (FDA), (2) contraceptive care, (3) sterilization procedures, and (4) patient education and counseling. The Department of Defense shall establish a uniform standard curriculum to be used in family planning education programs for all men and women members of the Armed Forces. Every military treatment facility, upon request, shall provide emergency contraception, information about FDA-approved methods of emergency contraception, and notification of confidentiality rights to any woman who: (1) states, or is accompanied by another individual who states, that the woman is a victim of sexual assault; or (2) is reasonably believed to be a survivor of sexual assault.
United States · United States Congress · 26 April 2017
Expresses support for efforts to: (1) exempt sunscreen from over-the-counter medication bans in schools, and (2) encourage health care professionals to educate parents and children about sun-safe behaviors. Encourages schools to allow students to possess sunscreen without restriction and without physician authorization.
United States · United States Congress · 26 April 2017
Regulatory Accountability Act of 2017 This bill codifies and revises notice-and-comment rulemaking procedures to require federal agencies to consider: (1) whether a rulemaking is required by statute or is within the discretion of the agency, (2) whether existing federal laws or rules could be amended or rescinded to address the problem, and (3) reasonable alternatives for a new rule. For major or high-impact rules, an agency must: publish a notice of initiation of rulemaking to invite interested parties to propose alternatives and ideas that accomplish the agency's objectives and benefit the public; allow persons interested in high-impact or certain major rules to petition for a public hearing with oral presentation, cross-examination, and the burden of proof on the proponent of the rule; adopt the most cost-effective rule among reasonable alternatives that meet statutory objectives, unless additional benefits justify additional costs; and publish a framework and metrics for measuring the effectiveness of the rule on an ongoing basis. The bill defines: a "high-impact rule" as a rule likely to cause an annual effect on the economy of $1 billion or more; and a "major rule" as a rule likely to cause an annual effect on the economy of $100 million or more, a major increase in costs or prices, or significant adverse effects on competition, employment, investment, productivity, innovation, public health and safety, or the ability of U.S.-based enterprises to compete with foreign-based enterprises. Agencies proposing a rule must notify the Office of Information and Regulatory Affairs (OIRA) and publish a notice of proposed rulemaking that includes: (1) a text of the proposed rule; (2) rulemaking considerations; and (3) for any major rule or high-impact rule, a discussion of alternatives and a preliminary explanation of how the rules meets statutory objectives and how benefits justify costs. When adopting a rule, an agency must publish a notice of final rulemaking that explains its determinations and responds to comments. To obtain public comment on whether rules adopted at the end of a presidential administration should be amended or rescinded, agencies may delay rules that have not yet become effective before the inauguration of a new President. OIRA must establish rulemaking guidelines for: (1) assessing costs and benefits, economic issues, and risk assessments; and (2) avoiding inconsistency or duplication with other agency rules. The bill revises the scope of judicial review to: (1) establish a substantial evidence standard for high-impact rules, (2) allow courts to remand a matter to an agency without setting aside the agency's action, and (3) prohibit review of a determination of whether a rule is a major rule based on an increase in costs or adverse effects. Agencies issuing guidance are: (1) prohibited from foreclosing consideration of issues, (2) required to state that guidance is not legally binding, and (3) required to confer with OIRA on major guidance.
United States · United States Congress · 26 April 2017
Medical Device Safety Act This bill amends the Federal Food, Drug, and Cosmetic Act to declare that an action for damages or a person's liability under state law is not affected by the federal prohibition on state or local requirements regarding medical devices. This bill is retroactively effective and applies to pending civil actions.
United States · United States Congress · 26 April 2017
Medical Device Guardians Act This bill amends the Federal Food, Drug, and Cosmetic Act to require physicians to report significant adverse experiences caused by medical devices to the Food and Drug Administration.
United States · United States Congress · 26 April 2017
This joint resolution amends the Continuing Appropriations Act, 2017 to provide continuing FY2017 appropriations for most federal agencies through the earlier of May 5, 2017, or the enactment of the applicable appropriations legislation. It is commonly referred to as a continuing resolution (CR) and prevents a partial government shutdown that would otherwise occur after the existing CR expires on April 28, 2017, because 11 of the 12 FY2017 regular appropriations bills that fund the federal government have not been enacted. (The Military Construction, Veterans Affairs, and Related Agencies Appropriations Act, 2017 was signed into law on September 29, 2016.) The CR also amends the Surface Mining Control and Reclamation Act of 1977 to extend through May 5, 2017, a provision that provides health care benefits for certain retired miners and their families.
United States · United States Congress · 25 April 2017
Veterans E-Health and Telemedicine Support Act of 2017 or the VETS Act of 2017 This bill allows a licensed health care professional of the Department of Veterans Affairs to practice his or her profession using telemedicine at any location in any state, regardless of where the professional or patient is located.
United States · United States Congress · 25 April 2017
Veterans E-Health and Telemedicine Support Act of 2017 or the VETS Act of 2017 This bill allows a licensed health care professional of the Department of Veterans Affairs to practice his or her profession using telemedicine at any location in any state, regardless of where the professional or patient is located.
United States · United States Congress · 25 April 2017
FDA Reauthorization Act of 2017 Prescription Drug User Fee Amendments of 2017 This bill amends the Federal Food, Drug, and Cosmetic Act to extend through FY2022 and revise Food and Drug Administration (FDA) user fees for new drug applications. User fees are eliminated for supplements to new drug applications and drug manufacturing facilities. Medical Device User Fee Amendments of 2017 The bill extends through FY2022 and revises FDA user fees for medical devices. A user fee is established for requests to classify devices that are not substantially equivalent to marketed devices. The FDA is no longer granted the discretion to waive or reduce fees in the interest of public health. The FDA must establish a pilot program to accredit testing laboratories to determine whether medical devices conform to performance standards. The bill revises the types of medical devices that the FDA may accredit third parties to review. Generic Drug User Fee Amendments of 2017 The bill extends through FY2022 and revises FDA user fees for generic drugs. User fees are eliminated for supplements to generic drug applications. An annual fee is assessed on holders of approved generic drug applications. Biosimilar User Fee Amendments of 2017 The bill extends through FY2022 and revises FDA user fees for biosimilars. (Biosimilars are biological products approved by the FDA based on their similarity to an already-approved biological product.) User fees are eliminated for supplements to biosimilar applications and biosimilar manufacturing facilities. An annual fee is assessed on holders of approved applications for biosimilars. The bill sets the annual amount of revenue that must be generated by fees. The bill extends through FY2022 programs and policies including Critical Path Public-Private Partnerships and support for development of medical products for rare conditions.
United States · United States Congress · 25 April 2017
Risk-Based Classification of Accessories Act of 2017 This bill revises how accessories to medical devices are classified. Specifically, the Food and Drug Administration must classify accessories based on the risks when used as intended , notwithstanding the classification of any other device with which such accessory is intended to be used.
United States · United States Congress · 25 April 2017
Medical Device Servicing Safety and Accountability Act This bill amends the Federal Food, Drug, and Cosmetic Act to require establishments servicing medical devices to register with the Food and Drug Administration (FDA). Such establishments must maintain records and make reports as the FDA requires to ensure the safety and effectiveness of serviced devices. The bill exempts certain medical facilities, including physician's offices, that service medical devices in accordance with state and local laws.
United States · United States Congress · 25 April 2017
Expresses support for the designation of National Stress Awareness Month. Recognizes the efforts made by the Department of Health and Human Services to educate people about the causes, symptoms, and treatment of stress.
United States · United States Congress · 25 April 2017
Designates April 2017 as Parkinson's Awareness Month. Expresses support for research to find better treatments and a cure for Parkinson's disease. Recognizes individuals living with Parkinson's disease who participate in clinical trials. Commends the dedication of organizations, volunteers, researchers, and millions of individuals across the United States working to improve the quality of life for individuals living with Parkinson's disease and their families.
United States · United States Congress · 24 April 2017
Protecting Patient Access to Emergency Medications Act of 2017 This bill amends the Controlled Substances Act to direct the Drug Enforcement Administration (DEA) to register an emergency medical services (EMS) agency to administer controlled substances if the agency submits an application demonstrating that it is authorized to conduct such activity in the state in which the agency practices. The DEA may deny an application if it determines that the registration is inconsistent with the public interest. An EMS agency may obtain a single registration in each state instead of a separate registration for each location. A registered EMS agency may deliver, store, and receive controlled substances, subject to specified conditions. An EMS professional of a registered EMS agency may administer controlled substances in schedules II, III, IV, or V outside the physical presence of a medical director if such administration is authorized under state law and pursuant to a standing or verbal order, subject to specified conditions. The bill specifies that a hospital-based EMS agency (i.e., an EMS agency owned or operated by a hospital) may continue to administer controlled substances under the hospital's DEA registration. A pharmacy may deliver a controlled substance to an administering practitioner in accordance with this bill's requirements, subject to specified conditions.
United States · United States Congress · 24 April 2017
National Clinical Care Commission Act This bill establishes within the Department of Health and Human Services (HHS) a National Clinical Care Commission to evaluate and make recommendations regarding improvements to the coordination and leveraging of federal programs related to complex metabolic or autoimmune diseases that result from issues related to insulin and represent a significant disease burden (e.g., diabetes). The commission must report on: (1) HHS programs that focus on prevention, (2) current activities and gaps in federal efforts to support clinicians in providing integrated care, (3) improvement in federal education and awareness activities related to prevention and treatment, and (4) methods for outreach and dissemination of education and awareness materials. The commission must submit an operating plan to HHS and Congress within 90 days of its first meeting. The commission is terminated after it submits a final report, but not later than the end of FY2021.
United States · United States Congress · 24 April 2017
Safe Drinking Water Assistance Act of 2017 This bill addresses contaminants of emerging concern (emerging contaminants), which are not regulated under a national primary drinking water regulation and may have an adverse effect on human health. The Environmental Protection Agency (EPA) must review federal efforts to: (1) identify, monitor, and assist in the development of treatment methods for emerging contaminants; and (2) assist states in responding to the human health challenges posed by those contaminants. In addition, the EPA must establish a strategic plan for improving those efforts. The EPA and the Department of Health and Human Services must jointly establish an interagency working group to coordinate federal activities that identify and analyze the public health effects of emerging contaminants. The Office of Science and Technology Policy must establish a National Emerging Contaminant Research Initiative for developing an interagency federal research strategy that specifies and prioritizes the research necessary to improve the identification, analysis, monitoring, and treatment methods of emerging contaminants. Specified federal agencies must make grants for research proposals selected by the initiative as likely to result in significant progress toward achieving the strategy's objectives. The EPA must: (1) report on actions it may take to increase support for states that require testing facilities for emerging contaminants in drinking water samples; and (2) develop a program, based on the report's findings, to provide assistance to eligible states for the testing and analysis of emerging contaminants.
United States · United States Congress · 20 April 2017
Speeding Access to Already Approved Pharmaceuticals Act of 2017 This bill amends the Federal Food, Drug, and Cosmetic Act to require the Food and Drug Administration to facilitate the development and expedite the review of a new drug, biological product, or medical device that has been approved in the European Union.
United States · United States Congress · 14 April 2017
GI Bill Fairness Act of 2017 This bill includes as active duty, for purposes of eligibility for post-9/11 veterans educational assistance, service of a member of a reserve component ordered to active duty to receive authorized medical care, to be medically evaluated, or to complete a required Department of Defense health care study.
United States · United States Congress · 12 April 2017
Empire State Equity Act This bill amends title XIX (Medicaid) of the Social Security Act to increase federal Medicaid funding for states that received, for FY2016, disproportionate share hospital (DSH) allotments greater than six times the national average. (DSHs are hospitals that receive additional payment under Medicaid for treating a large share of low-income patients.)
United States · United States Congress · 7 April 2017
This bill extends the policy entitling new federal employees who are veterans with a service-connected disability to a specified amount of leave for medical treatment for such disability to all Veterans Health Administration physicians, dentists, podiatrists, chiropractors, optometrists, registered nurses, physician assistants, and expanded-function dental auxiliaries.
United States · United States Congress · 7 April 2017
Designates April 2017 as National Congenital Diaphragmatic Hernia Awareness Month. (Congenital diaphragmatic hernia is a birth defect that occurs when the diaphragm fails to fully form, allowing abdominal organs to migrate into the chest cavity and preventing lung growth.) Encourages that steps should be taken to: raise awareness of and increase public knowledge about congenital diaphragmatic hernia (CDH); inform all Americans about the dangers of CDH; disseminate information on the importance of quality neonatal care for CDH patients; promote quality prenatal care and the use of ultrasounds to detect CDH in utero; and support research funding of CDH to improve screening and treatment, discover its causes, and develop a cure.
United States · United States Congress · 7 April 2017
This bill amends the Caregivers and Veterans Omnibus Health Services Act of 2010 to: (1) extend until September 30, 2019, the Department of Veterans Affairs (VA) pilot program on the use of community-based organizations and local and state government entities to coordinate and increase the availability of health care to veterans transitioning to civilian life, (2) authorize the VA to expand the program to include additional locations beyond the five locations originally selected, and (3) require the VA to submit a report by 180 days after the completion of the program on the advisability of continuing or expanding it.
United States · United States Congress · 7 April 2017
Expresses support for the goals and ideals of National Public Health Week. Recognizes the efforts of public health professionals, governments, tribes, and individuals in preventing disease and injury. Encourages increased efforts and the use of additional resources to improve the health of people in the United States and to make the United States the healthiest nation in one generation through greater opportunities to improve community health and by strengthening the public health system.
United States · United States Congress · 6 April 2017
Opioid Preventing Abuse through Continuing Education Act of 2017 or the Opioid PACE Act of 2017 This bill amends the Controlled Substances Act to require a practitioner (other than a hospital, pharmacy, pharmacist, or veterinarian) to comply with a training requirement, as a condition of obtaining or renewing a registration to prescribe or dispense opioids for the treatment of pain or pain management.
United States · United States Congress · 6 April 2017
Promoting Integrity in Medicare Act of 201 7 or the PIMA of 201 7 This bill expands Medicare's prohibition on physician self-referrals to include, with specified exceptions, certain advanced imaging, anatomic pathology, radiation therapy, and physical therapy services. Additionally, the bill establishes increased civil monetary penalties for violations of the self-referral prohibition with respect to those services. The Centers for Medicare & Medicaid Services shall conduct a compliance review with respect to such referrals.
United States · United States Congress · 6 April 2017
Medicare You Can Opt Into Act of 2017 This bill allows an individual to buy into Medicare for hospital insurance if the individual is residing in the United States and is a U.S. citizen, U.S. national, or permanent resident. The Department of Health and Human Services must establish enrollment periods and coverage for individuals who buy the insurance.