42 CFR 486, Subpart G - Requirements for Certification and Designation and Conditions for Coverage: Organ Procurement Organizations
- § 486.301 — Basis and scope.
- § 486.302 — Definitions.
- — Requirements for Certification and Designation
- § 486.303 — Requirements for certification.
- § 486.304 — Requirements for designation.
- § 486.306 — OPO service area size designation and documentation requirements.
- § 486.308 — Designation of one OPO for each service area.
- § 486.309 — Re-certification from August 1, 2006 through July 31, 2010.
- § 486.310 — Changes in control or ownership or service area.
- — Re-Certification and De-Certification
- § 486.312 — De-certification.
- § 486.314 — Appeals.
- § 486.316 — Re-certification and competition processes.
- — Organ Procurement Organization Outcome Requirements
- § 486.318 — Condition: Outcome measures.
- — Organ Procurement Organization Process Performance Measures
- § 486.320 — Condition: Participation in Organ Procurement and Transplantation Network.
- § 486.322 — Condition: Relationships with hospitals, critical access hospitals, and tissue banks.
- § 486.324 — Condition: Administration and governing body.
- § 486.326 — Condition: Human resources.
- § 486.328 — Condition: Reporting of data.
- § 486.330 — Condition: Information management.
- § 486.342 — Condition: Requesting consent.
- § 486.344 — Condition: Evaluation and management of potential donors and organ placement and recovery.
- § 486.346 — Condition: Organ preparation and transport.
- § 486.348 — Condition: Quality assessment and performance improvement (QAPI).
Title 42 published on 2012-10-01
The following are only the Rules published in the Federal Register after the published date of Title 42.
For a complete list of all Rules, Proposed Rules, and Notices view the Rulemaking tab.
This is a list of United States Code sections, Statutes at Large, Public Laws, and Presidential Documents, which provide rulemaking authority for this CFR Part.
This list is taken from the Parallel Table of Authorities and Rules provided by GPO [Government Printing Office].
It is not guaranteed to be accurate or up-to-date, though we do refresh the database weekly. More limitations on accuracy are described at the GPO site.
Title 42 published on 2012-10-01
The following are ALL rules, proposed rules, and notices (chronologically) published in the Federal Register relating to 42 CFR 486 after this date.
GPO FDSys XML | Text type regulations.gov FR Doc. 2013-02421 RIN 0938-AR49 CMS-3267-P DEPARTMENT OF HEALTH AND HUMAN SERVICES, Centers for Medicare & Medicaid Services Proposed rule. To be assured consideration, comments must be received at one of the addresses provided below, no later than 5 p.m. on April 8, 2013. 42 CFR Parts 416, 442, 482, 483, 485, 486, 488, 491, and 493 This proposed rule would reform Medicare regulations that CMS has identified as unnecessary, obsolete, or excessively burdensome on health care providers and suppliers, as well as certain regulations under the Clinical Laboratory Improvement Amendments of 1988 (CLIA). This proposed rule would increase the ability of health care professionals to devote resources to improving patient care, by eliminating or reducing requirements that impede quality patient care or that divert resources away from providing high quality patient care. This is one of several rules that we are proposing to achieve regulatory reforms under Executive Order 13563 on improving regulation and regulatory review and the Department's plan for retrospective review of existing rules.
GPO FDSys XML | Text type regulations.gov FR Doc. 2012-26900 RIN 0938-AR11 CMS-1590-FC DEPARTMENT OF HEALTH AND HUMAN SERVICES, Centers for Medicare & Medicaid Services Final rule with comment period. Effective date: The provisions of this final rule with comment period are effective on January 1, 2013 with the exception of provisions in § 410.38 which are effective on July 1, 2013. The incorporation by reference of certain publications listed in the rule was approved by the Director of the Federal Register on May 16, 2012. Comment date: To be assured consideration, comments must be received at one of the addresses provided below, no later than 5 p.m. on December 31, 2012. (See the SUPPLEMENTARY INFORMATION section of this final rule with comment period for a list of the provisions open for comment.) 42 CFR Parts 410, 414, 415, 421, 423, 425, 486, and 495 This major final rule with comment period addresses changes to the physician fee schedule, payments for Part B drugs, and other Medicare Part B payment policies to ensure that our payment systems are updated to reflect changes in medical practice and the relative value of services. It also implements provisions of the Affordable Care Act by establishing a face-to-face encounter as a condition of payment for certain durable medical equipment (DME) items. In addition, it implements statutory changes regarding the termination of non-random prepayment review. This final rule with comment period also includes a discussion in the Supplementary Information regarding various programs . (See the Table of Contents for a listing of the specific issues addressed in this final rule with comment period.)