Requests for Bids (RFB) for Durable Medical Equipment, Prosthetics, Orthotics, and Supplies (DMEPOS) Competitive Bidding Program

ICR 201305-0938-005

OMB: 0938-1016

Federal Form Document

Forms and Documents
Document
Name
Status
Form and Instruction
New
Form and Instruction
New
Form and Instruction
Modified
Form and Instruction
Modified
Form and Instruction
Modified
Form and Instruction
Removed
Form and Instruction
Removed
Supplementary Document
2013-05-10
Supplementary Document
2013-05-10
Supplementary Document
2012-07-25
Supplementary Document
2012-07-25
Supplementary Document
2012-07-25
Supplementary Document
2012-07-25
Supplementary Document
2012-07-25
Supplementary Document
2012-07-25
Supplementary Document
2012-07-25
Supplementary Document
2012-07-25
Supplementary Document
2012-07-25
Supplementary Document
2012-07-25
Supplementary Document
2012-07-25
Supplementary Document
2012-07-25
Supplementary Document
2012-07-25
Supplementary Document
2012-07-25
Supporting Statement A
2013-05-10
ICR Details
0938-1016 201305-0938-005
Historical Active 201207-0938-007
HHS/CMS 19556
Requests for Bids (RFB) for Durable Medical Equipment, Prosthetics, Orthotics, and Supplies (DMEPOS) Competitive Bidding Program
Revision of a currently approved collection   No
Regular
Approved without change 06/10/2013
Retrieve Notice of Action (NOA) 05/10/2013
  Inventory as of this Action Requested Previously Approved
06/30/2016 36 Months From Approved 10/31/2015
20,212 0 16,865
9,301 0 34,795
0 0 0

In preparing for the Round 2 and national mail-order competitions, CMS received OMB approval of this collection on November 2, 2011 with no material or non-substantive changes. The collection was modified from prior rounds of competitive bidding in order to make the documents more reader-friendly, to clarify the requirements that suppliers had difficulty in understanding, and to incorporate the Round 2 and national mail order bidding areas and product categories. CMS is currently re-competing the Round 1 Rebid areas. On 10/10/12, we received approval for a revision to a currently approved collection to extend the information collection for an additional three years. We are seeking OMB approval for a revision to this currently approved package as our program expands and increases the population from which we will be collecting information.

PL: Pub.L. 108 - 173 302(b)(1) Name of Law: Payment for durable medical equipment; competitive acquisition of certain items and services
   PL: Pub.L. 110 - 275 154 Name of Law: Delay in and Reform of Medicare DMEPOS Competitive Acquisition Program
  
PL: Pub.L. 110 - 275 154 Name of Law: Delay in and Reform of Medicare DMEPOS Competitive Acquisition Program

Not associated with rulemaking

  78 FR 13878 03/31/2013
78 FR 27399 05/10/2013
No

  Total Approved Previously Approved Change Due to New Statute Change Due to Agency Discretion Change Due to Adjustment in Estimate Change Due to Potential Violation of the PRA
Annual Number of Responses 20,212 16,865 203 3,144 0 0
Annual Time Burden (Hours) 9,301 34,795 157 -25,651 0 0
Annual Cost Burden (Dollars) 0 0 0 0 0 0
Yes
Changing Regulations
Yes
Changing Forms
Total burden associated with this ICR is increasing as the program expands in accordance with statutory mandates. Forms A and B are not part of this package but will be added before their use, upon OMB approval.

$1,437,666
No
No
Yes
No
No
Uncollected
Mitch Bryman 410 786-5258 [email protected]

  No

On behalf of this Federal agency, I certify that the collection of information encompassed by this request complies with 5 CFR 1320.9 and the related provisions of 5 CFR 1320.8(b)(3).
The following is a summary of the topics, regarding the proposed collection of information, that the certification covers:
 
 
 
 
 
 
 
    (i) Why the information is being collected;
    (ii) Use of information;
    (iii) Burden estimate;
    (iv) Nature of response (voluntary, required for a benefit, or mandatory);
    (v) Nature and extent of confidentiality; and
    (vi) Need to display currently valid OMB control number;
 
 
 
If you are unable to certify compliance with any of these provisions, identify the item by leaving the box unchecked and explain the reason in the Supporting Statement.
05/10/2013


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