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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 InfoFOR 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 InformationSUPPLEMENTARY 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:
Start SignatureTable 1—Summary of Benefits and Costs in 2018 Dollars Over a 10-Year Time Horizon
Category Primary estimate Low estimate High estimate Units Notes Year dollars Discount rate (%) Period covered Benefits: Annualized Monetized $/year 2018 2018 7 3 10 10 Annualized Quantified 7 3 Qualitative Disclosure of serious adverse events and outcomes related to investigational new drug treatments. Costs: Annualized Monetized $/year $5,694 $5,785 2018 2018 7 3 10 10 Annualized Quantified 7 3 Qualitative Transfers: Federal Annualized Monetized $/year 7 3 From/To From: To: Other Annualized Monetized $/year 7 3 From/To From: To: Effects: State, Local or Tribal Government: Small Business: Wages: Growth: Dated: August 20, 2020.
Lowell J. Schiller,
Principal Associate Commissioner for Policy.
[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