Reporting annual summaries under Right to Try Act

Right to Try Act: Reporting Requirements

Documents and Forms

Document Name Document Type
Form FDA 5023 Reporting annual summaries under Right to Try Act Form and Instruction
FDA 5023 Right-to-Try Annual Reporting 0893 Form FDA 5023 Right to Try Annual Summary.pdf Form and Instruction
FDA 5023 Right-to-Try Annual Reporting 0893 Form FDA 5023 Right to Try Annual Summary.pdf Form and Instruction

Information Collection (IC) Details

IC Title:	Reporting annual summaries under Right to Try Act	Agency IC Tracking Number:

Is this a Common Form? No		IC Status: Modified

Obligation to Respond: Required to Obtain or Retain Benefits

CFR Citation: 21 CFR 300.200

Information Collection Instruments:

Document Type	Form No.	Form Name	Instrument File	URL	Available Electronically?	Can Be Submitted Electronically?	Electronic Capability
Form and Instruction	FDA 5023	Right-to-Try Annual Reporting	0893 Form FDA 5023 Right to Try Annual Summary.pdf		Yes	Yes	Fillable Fileable

Line of Business: Health

Subfunction: Consumer Health and Safety

Privacy Act System of Records
Title:	FR Citation:

Number of Respondents: 6	Number of Respondents for Small Entity: 0

Affected Public: Private Sector	Private Sector: Businesses or other for-profits

Percentage of Respondents Reporting Electronically: 100 %

	Approved	Previously Approved
Annual Number of Responses for this IC	6	6
Annual IC Time Burden (Hours)	15	15
Annual IC Cost Burden (Dollars)	0	0

Documents for IC

Title	Document	Date Uploaded
No associated records found

Blank fields in records indicate information that was not collected or not collected electronically prior to July 2006.