2020-18777. Annual Summary Reporting Requirements Under the Right To Try Act; Correction  

  • Start Preamble Start Printed Page 55802

    AGENCY:

    Food and Drug Administration, HHS.

    ACTION:

    Proposed rule; correction.

    SUMMARY:

    The Food and Drug Administration (FDA, the Agency, or we) is correcting a proposed rule that published in the Federal Register of July 24, 2020. That proposed rule proposes to establish requirements for the deadline and contents of submission in an annual summary. We are placing a corrected copy of the proposed rule in the docket.

    Start Further Info

    FOR FURTHER INFORMATION CONTACT:

    Kathleen Davies, Food and Drug Administration, 10903 New Hampshire Ave., Bldg. 32, Rm. 3121, Silver Spring, MD 20993, 301-796-2205, kathleen.davies@fda.hhs.gov.

    End Further Info End Preamble Start Supplemental Information

    SUPPLEMENTARY INFORMATION:

    In the Federal Register of July 24, 2020, (85 FR 44803), FDA published the proposed rule “Annual Summary Reporting Requirements Under the Right to Try Act” with several errors.

    In the Federal Register of July 24, 2020, FR Doc. 2020-16016, the following corrections are made:

    On page 44804, in the third column, in section “D. Costs and Benefits” the first paragraph, the fourth and fifth sentences are corrected as follows: “The total estimated present value of this rule's costs is $39,991 at a seven percent discount rate and $49,345 at a three percent discount rate (in 2018 dollars). The annualized cost of this rule over 10 years is $5,694 at a seven percent discount rate and $5,785 at a three percent discount rate.” On page 44808, in table 1, in column 2 (“Primary estimate”) rows 4 and 5 (“Costs” category) are corrected as follows: “$5,694” and $5,785”, respectively, and the “7” in column 4 (“High estimate”) is removed. On pages 44808 and 44809, in column 6 (“Discount Rate (10%)”) is corrected to read as follows:

    Table 1—Summary of Benefits and Costs in 2018 Dollars Over a 10-Year Time Horizon

    CategoryPrimary estimateLow estimateHigh estimateUnitsNotes
    Year dollarsDiscount rate (%)Period covered
    Benefits:
    Annualized Monetized $/year2018 20187 310 10
    Annualized Quantified7 3
    QualitativeDisclosure of serious adverse events and outcomes related to investigational new drug treatments.
    Costs:
    Annualized Monetized $/year$5,694 $5,7852018 20187 310 10
    Annualized Quantified7 3
    Qualitative
    Transfers:
    Federal Annualized Monetized $/year7 3
    From/ToFrom:To:
    Other Annualized Monetized $/year7 3
    From/ToFrom:To:
    Effects:State, Local or Tribal Government:
    Small Business:
    Wages:
    Growth:
    Start Signature

    Dated: August 20, 2020.

    Lowell J. Schiller,

    Principal Associate Commissioner for Policy.

    End Signature End Supplemental Information

    [FR Doc. 2020-18777 Filed 9-9-20; 8:45 am]

    BILLING CODE 4164-01-P

Document Information

Published:
09/10/2020
Department:
Food and Drug Administration
Entry Type:
Proposed Rule
Action:
Proposed rule; correction.
Document Number:
2020-18777
Pages:
55802-55802 (1 pages)
Docket Numbers:
Docket No. FDA-2019-N-5553
RINs:
0910-AI36: Annual Summary Reporting Requirements Under the Right to Try Act
RIN Links:
https://www.federalregister.gov/regulations/0910-AI36/annual-summary-reporting-requirements-under-the-right-to-try-act
PDF File:
2020-18777.pdf
Supporting Documents:
» Annual Summary Reporting Requirements Under the Right to Try Act
» Annual Summary Reporting Requirements Under the Right to Try Act: Correction
» Annual Summary Reporting Requirements Under the Right to Try Act
CFR: (1)
21 CFR 300