U.S. Food and Drug Administration

Publish Date

Mon, 12/02/2019 - 11:51

Review Date

Mon, 12/02/2024 - 00:00

Last Reviewed Date

Mon, 12/02/2019 - 00:00

Next Review Date

5 Years

Short Title

MedWatch: Information and Adverse Event Reporting Program - Voluntary

Detailed Description

MedWatch: Information and Adverse Event Reporting Program - Voluntary

Short Description

MedWatch: Information and Adverse Event Reporting Program - Voluntary

Center

Office of the Commissioner

Content Owner

Office of the Commissioner

Site Structure

Forms

Source Organization

FDA

Download Type

Form

Form Name

MedWatch: Information and Adverse Event Reporting Program - Voluntary (HTML)

Form ID

3500

Form Issue Date

Fri, 02/01/2019 - 13:19

OMB Form Approval

0910-0291

Interactive Form

Off

Bulk Approved

Off

Display Short Description

Off

Old URL

https://www.fda.gov/downloads/AboutFDA/ReportsManualsForms/Forms/UCM522074.htm

Contact

CDER Drug Info: (888) 463-633

Author

eaw

Contact

CDER Drug Info: (888) 463-6332