Improving the Efficiency of Clinical Trials for Drug and Medical Device Development

ASPE Generic Clearance for the Collection of Qualitative Research and Assessment

⚠️ Notice: This information collection may be referencing outdated material. More recent filings for OMB 0990-0421 can be found here:

Documents and Forms

Document Name Document Type
Clinical Trials Expert Questionnaire with Codes_171027.docx Other-survey
Cover Sheet 0990-0421_Clinical Trial Expert Questionnaire_final.docx memo v2 IC Document

Information Collection (IC) Details

IC Title:	Improving the Efficiency of Clinical Trials for Drug and Medical Device Development	Agency IC Tracking Number:

IC Status: New

Obligation to Respond: Voluntary

CFR Citation:

Information Collection Instruments:

Document Type	Form No.	Form Name	Instrument File	URL	Available Electronically?	Can Be Submitted Electronically?	Electronic Capability
Other-survey			Clinical Trials Expert Questionnaire with Codes_171027.docx		Yes	Yes	Fillable Fileable

Line of Business: Health

Subfunction: Health Care Services

Privacy Act System of Records
Title:	FR Citation:

Number of Respondents: 40	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	Program Change Due to Agency Discretion
Annual Number of Responses for this IC	40	40
Annual IC Time Burden (Hours)	40	40
Annual IC Cost Burden (Dollars)	0	0

Documents for IC

Title	Document	Date Uploaded
memo v2	Cover Sheet 0990-0421_Clinical Trial Expert Questionnaire_final.docx	12/04/2017

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