Information Collection

Guidance for Industry: Fast Track Drug Development Programs - Designation, Development, and Application Review (Premeeting Packages)

IC 6040 under ICR 201108-0910-002 · OMB 0910-0389.

⚠️ Notice: This information collection may be referencing outdated material. More recent filings for OMB 0910-0389 can be found here:

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Information Collection (IC) Details

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IC Title:	Guidance for Industry: Fast Track Drug Development Programs - Designation, Development, and Application Review (Premeeting Packages)	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 356(C) (To search for a specific CFR, visit the Code of Federal Regulations.)

Information Collection Instruments:

Document Type	Form No.	Form Name	Instrument File	URL	Available Electronically?	Can Be Submitted Electronically?	Electronic Capability

Line of Business: Health

Subfunction: Public Health Monitoring

Privacy Act System of Records
Title:	FR Citation:

Number of Respondents: 64	Number of Respondents for Small Entity: 0

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

Percentage of Respondents Reporting Electronically: 10 %

	Approved	Change Due to Adjustment in Agency Estimate	Previously Approved
Annual Number of Responses for this IC	77	0	77
Annual IC Time Burden (Hours)	7,700	3,080	4,620
Annual IC Cost Burden (Dollars)	0	0	0

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