Fda 1571 - Investigational New Drug Application (Ind) Page 3
Download a blank fillable Fda 1571 - Investigational New Drug Application (Ind) in PDF format just by clicking the "DOWNLOAD PDF" button.
Open the file in any PDF-viewing software. Adobe Reader or any alternative for Windows or MacOS are required to access and complete fillable content.
Complete Fda 1571 - Investigational New Drug Application (Ind) with your personal data - all interactive fields are highlighted in places where you should type, access drop-down lists or select multiple-choice options.
Some fillable PDF-files have the option of saving the completed form that contains your own data for later use or sending it out straight away.
ADVERTISEMENT
1
2
3The information below applies only to requirements of the Paperwork Reduction Act of 1995.
Department of Health and Human Services
The burden time for this collection of information is estimated to average 100 hours per
Food and Drug Administration
response, including the time to review instructions, search existing data sources, gather
Office of Operations
and maintain the data needed and complete and review the collection of information. Send
Paperwork Reduction Act (PRA) Staff
comments regarding this burden estimate or any other aspect of this information collection,
PRAStaff@fda.hhs.gov
including suggestions for reducing this burden to the address to the right:
“An agency may not conduct or sponsor, and a person is not required to respond to, a
Please do NOT send your completed form
collection of information unless it displays a currently valid OMB number.”
to this PRA Staff email address.
FORM FDA 1571 (2/16)
Page 3 of
3
ADVERTISEMENT
0 votes
Related Articles
Related forms
Related Categories
Parent category: Legal