The Food and Drug Administration (FDA) is requesting approval of a new generic for collecting information through the use of qualitative methods for studies about tobacco products. FDA will employ qualitative research, including individual in-depth interviews (IDIs), small group discussions, and focus groups to explore knowledge and perceptions about tobacco-related topics with specific target audiences. FDA will only submit an individual generic collection for approval under this generic clearance if the individual collection meets the outlined conditions.
The latest form for Generic Clearance for the Collection of Qualitative Data on Tobacco Products and Communications expires 2021-07-31 and can be found here.
Document Name |
---|
Supplementary Document |
Supplementary Document |
Justification for No Material/Nonsubstantive Change |
Supplementary Document |
Supporting Statement B |
Supporting Statement A |
Extension without change of a currently approved collection | 2024-07-05 | ||
Approved without change |
No material or nonsubstantive change to a currently approved collection | 2022-11-22 | |
Approved without change |
Extension without change of a currently approved collection | 2021-06-16 | |
Approved without change |
No material or nonsubstantive change to a currently approved collection | 2020-07-13 | |
Approved without change |
No material or nonsubstantive change to a currently approved collection | 2020-02-06 | |
Approved with change |
Extension without change of a currently approved collection | 2018-05-17 | |
Approved with change |
New collection (Request for a new OMB Control Number) | 2014-12-10 |
Federal Enterprise Architecture: Health - Consumer Health and Safety