This program will obtain data on safety information to support quick-turnaround decision-making about potential safety problems or risk management solutions. This information will be collected from health professionals, hospitals, and other user facilities (e.g., nursing homes, ambulatory surgical facilities and outpatient diagnostic and treatment facilities, etc.), consumers, sponsors and manufacturers of biologics, drugs and medical products, distributors, and importers when FDA must quickly determine whether or not a problem with a medical product impacts the public health.
The latest form for Rapid Response Surveys expires 2023-09-30 and can be found here.
Approved without change |
Extension without change of a currently approved collection | 2020-08-25 | |
Approved without change |
Extension without change of a currently approved collection | 2017-06-30 | |
Approved without change |
Extension without change of a currently approved collection | 2014-04-23 | |
Approved with change |
Revision of a currently approved collection | 2010-12-20 | |
Approved with change |
Extension without change of a currently approved collection | 2007-10-11 | |
Withdrawn and continue |
No material or nonsubstantive change to a currently approved collection | 2007-09-07 | |
Approved without change |
Extension without change of a currently approved collection | 2006-03-31 | |
Approved without change |
No material or nonsubstantive change to a currently approved collection | 2005-09-28 | |
Approved with change |
Extension without change of a currently approved collection | 2004-05-10 | |
Approved with change |
New collection (Request for a new OMB Control Number) | 2002-10-30 |