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Agency Information Collection Activities; Submission for Office of Management and Budget Review; Comment Request; Mammography Quality Standards Act Requirements

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AGENCY:

Food and Drug Administration, HHS.

ACTION:

Notice.

SUMMARY:

The Food and Drug Administration (FDA) is announcing that a proposed collection of information has been submitted to the Office of Management and Budget (OMB) for review and clearance under the Paperwork Reduction Act of 1995.

DATES:

Fax written comments on the collection of information by September 19, 2016.

ADDRESSES:

To ensure that comments on the information collection are received, OMB recommends that written comments be faxed to the Office of Information and Regulatory Affairs, OMB, Attn: FDA Desk Officer, FAX: 202-395-7285, or emailed to oira_submission@omb.eop.gov. All comments should be identified with the OMB control number 0910-0309. Also include the FDA docket number found in brackets in the heading of this document.

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FOR FURTHER INFORMATION CONTACT:

FDA PRA Staff, Office of Operations, Food and Drug Administration, Three White Flint North,10A-12M, 11601 Landsdown St., North Bethesda, MD 20852, PRAStaff@fda.hhs.gov.

End Further Info End Preamble Start Supplemental Information

SUPPLEMENTARY INFORMATION:

In compliance with 44 U.S.C. 3507, FDA has submitted the following proposed collection of information to OMB for review and clearance.

Mammography Quality Standards Act Requirements—21 CFR Part 900, OMB Control Number 0910-0309—Extension

The Mammography Quality Standards Act (Pub. L. 102-539) requires the establishment of a Federal certification and inspection program for mammography facilities; regulations and standards for accreditation and certification bodies for mammography facilities; and standards for mammography equipment, personnel, and practices, including quality assurance. The intent of these regulations is to assure safe, reliable, and accurate mammography on a nationwide level. Under the regulations, as a first step in becoming certified, mammography facilities must become accredited by an FDA-approved accreditation body (AB). This requires undergoing a review of their clinical images and providing the AB with information showing that they meet the equipment, personnel, quality assurance, and quality control standards, and have a medical reporting and recordkeeping program, a medical outcomes audit program, and a consumer complaint mechanism. On the basis of this accreditation, facilities are then certified by FDA or an FDA-approved State certification agency and must prominently display their certificate. These actions are taken to ensure safe, accurate, and reliable mammography on a nationwide basis.

The following sections of Title 21 of the Code of Federal Regulations (CFR) are not included in the burden tables because they are considered usual and customary practice and were part of the standard of care prior to the implementation of the regulations. Therefore, they resulted in no additional burden: 21 CFR 900.12(c)(1) and (3) and 900.3(f)(1). Section 900.24(c) was also not included in the burden tables because if a certifying State had its approval withdrawn, FDA would take over certifying authority for the affected facilities. Because FDA already has all the certifying State's electronic records, there wouldn't be an additional reporting burden.

We have rounded numbers in the “Total Hours” column in all three burden tables. (Where the number was a portion of 1 hour, it has been rounded to 1 hour. All other “Total Hours” have been rounded to the nearest whole number.)Start Printed Page 55464

We do not expect any respondents for § 900.3(c) because all four ABs are approved until April 2020.

In the Federal Register of June 8, 2016 (81 FR 36924), FDA published a 60-day notice requesting public comment on the proposed collection of information. No comments were received.

FDA estimates the burden of this collection of information as follows:

Table 1—Estimated Annual Reporting Burden

Activity/21 CFR Section/Form FDA No.Number of respondentsNumber of responses per respondentTotal annual responsesAverage burden per responseTotal hours 1Total capital costs (in dollars)Total operating and maintenance costs (in dollars)
Notification of intent to become an AB—900.3(b)(1)0.3310.3311
Application for approval as an AB; full 2—900.3(b)(3)0.3310.3332010610,000
Application for approval as an AB; limited 3—900.3(b)(3)51530150
AB renewal of approval—900.3(c)010151
AB application deficiencies—900.3(d)(2)0.110.1303
AB resubmission of denied applications—900.3(d)(5)0.110.1303
Letter of intent to relinquish accreditation authority—900.3(e)0.110.111
Summary report describing all facility assessments—900.4(f)330133072,31077,600
AB reporting to FDA; facility 4—900.4(h)8,65418,65418,6544,327
AB reporting to FDA; AB 5—900.4(h)5151050
AB financial records—900.4(i)(2)1111616
Former AB new application—900.6(c)(1)0.110.1606
Reconsideration of accreditation following appeal—900.15(d)(3)(ii)11122
Application for alternative standard—900.18(c)21224
Alternative standard amendment—900.18(e)10110110
Certification agency application—900.21(b)0.3310.33320106208
Certification agency application deficiencies—900.21(c)(2)0.110.1303
Certification electronic data transmission—900.22(h)520010000.0838330,000
Changes to standards—900.22(i)212306020
Certification agency minor deficiencies—900.24(b)1113030
Appeal of adverse action taken by FDA—900.25(a)0.210.2163
Inspection fee exemption—Form FDA 342270017000.25175
Total11,77740,00082,155
1 Total hours have been rounded.
2 One time burden.
3 Refers to accreditation bodies applying to accredit specific full-field digital mammography units.
4 Refers to the facility component of the burden for this requirement.
5 Refers to the AB component of the burden for this requirement.

Table 2—Estimated Annual Recordkeeping Burden

Activity/21 CFR SectionNumber of recordkeepersNumber of records per recordkeeperTotal annual recordsAverage burden per recordkeepingTotal hours 1Total capital costs (in dollars)Total operating and maintenance costs (in dollars)
AB transfer of facility records—900.3(f)(1)0.110.101
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Consumer complaints system; AB—900.4(g)51515
Documentation of interpreting physician initial requirements—900.12(a)(1)(i)(B)(2)871878696
Documentation of interpreting physician personnel requirements—900.12(a)(4)8,654434,616134,616
Permanent medical record—900.12(c)(4)8,65418,65418,65428,000
Procedures for cleaning equipment—900.12(e)(13)8,65452450,0080.08337,351
Audit program—900.12(f)8,65418,65416138,464
Consumer complaints system; facility—900.12(h)(2)8,654217,308117,308
Certification agency conflict of interest—900.22(a)51515
Processes for suspension and revocation of certificates—900.22(d)51515
Processes for appeals—900.22(e)51515
Processes for additional mammography review—900.22(f)51515
Processes for patient notifications—900.22(g)3131330
Evaluation of certification agency—900.2351520100
Appeals—900.25(b)51515
Total237,22328,00030
1 Total hours have been rounded.

Table 3—Estimated Annual Third-Party Disclosure Burden 1

Activity/21 CFR SectionNumber of respondentsNumber of disclosures per respondentTotal annual disclosuresAverage burden per disclosureTotal hours 2Total operating and maintenance costs (in dollars)
Notification of facilities that AB relinquishes its accreditation—900.3(f)(2)0.110.12002050
Clinical images; facility 3—900.4(c), 900.11(b)(1) and (2)2,88512,8851.444,154
Clinical images; AB 4—900.4(c)5154162,080230,773
Phantom images; facility 3—900.4(d), 900.11(b)(1) and (2)2,88512,8850.722,077
Phantom images; AB 4—900.4(d)5152081,040
Annual equipment evaluation and survey; facility 3—900.4(e), 900.11(b)(1) and (2)8,65418,65418,6548,654
Annual equipment evaluation and survey; AB 4—900.4(e)5151,7308,650
Provisional mammography facility certificate extension application—900.11(b)(3)0100.51
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Mammography facility certificate reinstatement application—900.11(c)312131251,56024,000,000
Lay summary of examination—900.12(c)(2)8,6545,08544,055,5900.0833,652,464
Lay summary of examination; patient refusal 5—900.12(c)(2)871870.544
Report of unresolved serious complaints—900.12(h)(4)20120120
Information regarding compromised quality; facility 3—900.12(j)(1)201202004,000300
Information regarding compromised quality; AB 4—900.12(j)(1)201203206,400600
Patient notification of serious risk—900.12(j)(2)51510050019,375
Reconsideration of accreditation—900.15(c)515210
Notification of requirement to correct major deficiencies—900.24(a)0.410.42008068
Notification of loss of approval; major deficiencies—900.24(a)(2)0.1510.151001525.50
Notification of probationary status—900.24(b)(1)0.310.32006051
Notification of loss of approval; minor deficiencies—900.24(b)(3)0.1510.151001525.50
Total3,691,84224,259,921
1 There are no capital costs associated with this collection of information.
2 Total hours have been rounded.
3 Refers to the facility component of the burden for this requirement.
4 Refers to the AB component of the burden for this requirement.
5 Refers to the situation where a patient specifically does not want to receive the lay summary of her exam.
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Dated: August 15, 2016.

Peter Lurie,

Associate Commissioner for Public Health Strategy and Analysis.

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[FR Doc. 2016-19808 Filed 8-18-16; 8:45 am]

BILLING CODE 4164-01-P