Clinical Laboratory Fee Schedule; Signature on Requisition

Docket ID: CMS-2011-0134
Agency: Centers for Medicare Medicaid Services (CMS)
Parent Agency: Department of Health and Human Services (HHS)
This proposed rule would address the signature requirement on requisitions for clinical diagnostic laboratory tests paid under the Clinical Laboratory Fee Schedule (CLFS) originally established in the CY 2011 Physician Fee Schedule final rule published on November 29, 2010.
RIN: 0938-AR06
Impacts and Effects: None
CFR Citation: 42 CFR 410
Priority: Info./Admin./Other
UA and Regulatory Plan Information open glossary dialog  
Publication Period: Fall 2011
Agenda Stage of Rulemaking: Completed Action
Major Rule: No
Legal Authorities: Social Security Act
Legal Deadlines: None
Government Levels Affected: No
Federalism Implications: No
Unfunded Mandates: No
Requires Regulatory Flexibility Analysis: No
Small Entities Affected: No
International Impacts: No
Energy Effects: No
Included in Regulatory Plan: No
ActionDateFR Citation
NPRM06/30/201176 FR 38342
Merged With 0938-AQ2507/22/2011
NPRM Comment Period End08/29/2011
Docket Details open glossary dialog  
Related RINs: None
Related Dockets: None
Type: Rulemaking

Primary Documents

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Comment Period Closed
Aug 29, 2011 11:59 PM ET
Proposed Rule
Posted: 06/30/2011
ID: CMS-2011-0134-0001
Comment Period Closed
Proposed Rule
Posted: 10/17/2011
ID: CMS-2011-0134-0058
Comment Period Closed
Proposed Rule
Posted: 10/17/2011
ID: CMS-2011-0134-0056
Comment Period Closed
Proposed Rule
Posted: 10/17/2011
ID: CMS-2011-0134-0059
Comment Period Closed
Proposed Rule
Posted: 10/17/2011
ID: CMS-2011-0134-0057

Supporting Documents

No documents available.


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Comments Received*
Regulatory Timeline
Pre Rule
Current Stage
Proposed Rule
Current Stage
Final Rule
Current Stage
Current Stage
Agency Contact
Glenn McGuirk
Health Insurance Specialist
Mail Stop C4-01-26 7500 Security Boulevard
Baltimore, MD 21244
*This count refers to the total comment/submissions received on this docket, as of 11:59 PM yesterday. Note: Agencies review all submissions, however some agencies may choose to redact, or withhold, certain submissions (or portions thereof) such as those containing private or proprietary information, inappropriate language, or duplicate/near duplicate examples of a mass-mail campaign. This can result in discrepancies between this count and those displayed when conducting searches on the Public Submission document type. For specific information about an agency’s public submission policy, refer to its website or the Federal Register document.