AGENCY |
FORM # |
FORM NAME |
TYPE |
REVISED |
FDA
|
1571
|
Investigational New Drug Application (IND)
|
Form Only
|
Apr 01, 2006
|
FDA
|
1572
|
Statement of Investigator
|
Instructions Only
|
May 01, 2006
|
FDA
|
1572
|
Statement of Investigator
|
Form Only
|
May 01, 2006
|
FDA
|
1815
|
Certificate/Transmittal for an Application
|
Form Only
|
Feb 01, 2006
|
FDA
|
1932
|
Veterinary Adverse Drug Reaction, Lack of Effectiveness, Product Defect Report
|
Form Only
|
Jan 01, 2007
|
FDA
|
1932
a
|
Veterinary Adverse Drug Reaction, Lack of Effectiveness or Product Defect Report
|
Form Only
|
Mar 01, 2007
|
FDA
|
1993
|
Application for Permit to Ship or Transport Milk and/or Cream into US
|
Form Only
|
Feb 01, 2006
|
FDA
|
1994
|
Report of Tuberculin Tests of Cattle
|
Form Only
|
Feb 01, 2006
|
FDA
|
1995
|
Report of Physical Examination of Cows
|
Form Only
|
Feb 01, 2006
|
FDA
|
1996
|
Dairy Farm Sanitation Report
|
Form Only
|
Feb 01, 2006
|
FDA
|
1997
|
Score Card for Sanitation Inspections of Milk Plants
|
Form Only
|
Feb 01, 2006
|
FDA
|
2252
|
Transmittal of Annual Report for Drugs and Biologics for Human Use
|
Form Only
|
Jun 01, 2005
|
FDA
|
2253
|
Transmittal of Advertisements and Promotional Labeling for Drugs And Biologics For Human Use
|
Form Only
|
Jun 01, 2008
|
FDA
|
2253
|
Transmittal of Advertisements and Promotional Labeling for Drugs And Biologics For Human Use
|
Form Only
|
Oct 01, 2007
|
FDA
|
2301
|
Transmittal of Periodic Reports and Promotional Material for New Animal Drugs
|
Form Only
|
Mar 01, 2007
|
FDA
|
2511
|
Registration of Cosmetic Product Establishment
|
Instructions Only
|
Jun 01, 2006
|
FDA
|
2511
|
Registration of Cosmetic Product Establishment
|
Form Only
|
Jun 01, 2006
|
FDA
|
2512
|
Cosmetic Product Ingredient Statement
|
Form Only
|
Jun 01, 2006
|
FDA
|
2512
|
Cosmetic Product Ingredient Statement
|
Instructions Only
|
Jun 01, 2006
|
FDA
|
2512
a
|
Cosmetic Product Ingredient Statement
|
Form Only
|
Jun 01, 2006
|
FDA
|
2512
a
|
Cosmetic Product Ingredient Statement
|
Instructions Only
|
Jun 01, 2006
|
FDA
|
2514
|
Notice of Discontinuance of Commercial Distribution. of Cosmetic Product Formulation
|
Form Only
|
Jun 01, 2006
|
FDA
|
2514
|
Notice of Discontinuance of Commercial Distribution. of Cosmetic Product Formulation
|
Instructions Only
|
Jun 01, 2006
|
FDA
|
2541
a
|
Food Process Filing For All Methods Except Low-Acid Aseptic
|
Instructions Only
|
Oct 01, 2003
|
FDA
|
2541
c
|
Food Process Filing For Low-Acid Aseptic Systems
|
Form Only
|
Aug 01, 2005
|
FDA
|
2541
|
Food Canning Registration
|
Instructions Only
|
Oct 01, 2005
|
FDA
|
2541
a
|
Food Process Filing For All Methods Except Low-Acid Aseptic
|
Form Only
|
Oct 01, 2003
|
FDA
|
2541
c
|
Food Process Filing For Low-Acid Aseptic Systems
|
Instructions Only
|
Aug 01, 2005
|
FDA
|
2541
|
Food Canning Registration
|
Form Only
|
Oct 01, 2005
|
FDA
|
2567
|
Transmittal of Labels & Circulars
|
Form Only
|
Oct 01, 2005
|
FDA
|
2656
|
Registration Of Drug Establishment/Labeler Code Assignment
|
Instructions Only
|
Aug 01, 2007
|
FDA
|
2656
|
Registration Of Drug Establishment/Labeler Code Assignment
|
Form Only
|
Aug 01, 2007
|
FDA
|
2657
|
Drug Product Listing
|
Both Form and Instructions
|
Feb 01, 2005
|
FDA
|
2657
|
Drug Product Listing
|
Both Form and Instructions
|
Feb 01, 2008
|
FDA
|
2658
|
Registered Establishments Report of Private Label Distributors
|
Both Form and Instructions
|
Aug 01, 2007
|
FDA
|
2767
|
Notice of Availability of Sample Electronic Product
|
Form Only
|
May 01, 2007
|
FDA
|
2830
|
Blood Establishment Registration and Product Listing
|
Form Only
|
Jul 01, 2006
|
FDA
|
2877
|
Declaration for Imported Electronic Products Subject to Radiation Control Standards
|
Form Only
|
Dec 01, 2003
|
FDA
|
2914
|
Radioactive Drug Research Committee (RDRC) Report on Research Use of Radioactive Drugs Membership Summary
|
Form Only
|
Nov 01, 2006
|
FDA
|
2914
|
Radioactive Drug Research Committee (RDRC) Report on Research Use of Radioactive Drugs Membership Summary
|
Form Only
|
Aug 01, 2008
|
FDA
|
2915
|
Report on Research Use of Radioactive Drug Study Summary
|
Form Only
|
Nov 01, 2006
|
FDA
|
3038
|
Interstate Shellfish Dealer's Certificate
|
Form Only
|
Mar 01, 2007
|
FDA
|
3147
|
Application for a Variance From 21 CFR 1040.11(c) for a Laser Light Show, Display, or Device
|
Form Only
|
Dec 01, 2003
|
FDA
|
3331
|
NDA Field Alert Report
|
Form Only
|
Feb 01, 2006
|
FDA
|
3356
|
Establishment Registration and Listing for Human Cells, Tissues, and Celllular and Tissue-Based Products
|
Form Only
|
Apr 01, 2008
|
FDA
|
3397
|
User Fee Cover Sheet
|
Both Form and Instructions
|
Jan 01, 2007
|
FDA
|
3419
|
Medical Device Reporting Annual User Facility Report
|
Instructions Only
|
Oct 01, 2007
|
FDA
|
3419
|
Medical Device Reporting Annual User Facility Report
|
Form Only
|
Oct 01, 2007
|
FDA
|
3422
|
Government Entity Declaration
|
Form Only
|
Aug 01, 2007
|
FDA
|
3427
|
Supplemental Data Sheet
|
Form Only
|
Jan 01, 2003
|
FDA
|
3429
|
General Device Classification Questionnaire
|
Form Only
|
Jan 01, 2003
|
FDA
|
3448
|
Medicated Feed Mill License Application
|
Form Only
|
Sep 01, 2007
|
FDA
|
3454
|
Certification: Financial Interests and Arrangements Clinical Investigators
|
Form Only
|
Apr 01, 2006
|
FDA
|
3455
|
Disclosure: Financial Interests and Arrangements Clinical Investigators
|
Form Only
|
Apr 01, 2006
|
FDA
|
3458
|
Notice of Claimed Investigational Exemption
|
Form Only
|
Jul 01, 2007
|
FDA
|
3458
|
Notice of Claimed Investigational Exemption
|
Instructions Only
|
Jul 01, 2007
|
FDA
|
3479
|
Notification for a Food Contact Substance Formulation
|
Form Only
|
Mar 01, 2005
|
FDA
|
3480
|
Notification For New Use Of A Food Contact Substance
|
Form Only
|
Sep 01, 2005
|
FDA
|
3486
|
Biological Product Deviation Report
|
Instructions Only
|
Aug 01, 2007
|
FDA
|
3486
|
Biological Product Deviation Report
|
Form Only
|
Aug 01, 2007
|
FDA
|
3487
|
Notice of Final Disposition of Animals not Intended for Immediate Slaughter
|
Both Form and Instructions
|
Jul 01, 2007
|
FDA
|
3488
|
Notice of Intent to Slaughter for Human Food Purposes
|
Both Form and Instructions
|
Jul 07, 2007
|
FDA
|
3489
|
Request for a Meeting or Teleconference
|
Both Form and Instructions
|
Jul 07, 2007
|
FDA
|
3500
|
MedWatch: The FDA Safety Information and Adverse Event Reporting Program- Voluntary
|
Both Form and Instructions
|
Oct 01, 2005
|
FDA
|
3500
A
|
MedWatch: The FDA Safety Information and Adverse Event Reporting Program - Mandatory
|
Instructions Only
|
Oct 01, 2005
|
FDA
|
3500
A
|
MedWatch: FDA Medical Products Reporting Program - Mandatory
|
Form Only
|
Oct 01, 2005
|
FDA
|
3503
|
Food Additive Petition Submission
|
Form Only
|
Sep 01, 2007
|
FDA
|
3504
|
Color Additive Petition Submission
|
Form Only
|
Sep 01, 2007
|
FDA
|
3514
|
CDRH Premarket Review Submission Cover Sheet
|
Form Only
|
Mar 01, 2008
|
FDA
|
3514
|
CDRH Premarket Review Submission Cover Sheet
|
Form Only
|
Sep 01, 2007
|
FDA
|
3536
|
Protocol for Non-Clinical Laboratory and Effectiveness Studies
|
Both Form and Instructions
|
Jul 01, 2007
|
FDA
|
3537
|
Food Facility Registration
|
Form Only
|
May 01, 2007
|
FDA
|
3537
|
Food Facility Registration
|
Instructions Only
|
May 01, 2007
|
FDA
|
3537
a
|
Cancellation of Food Facility Registration
|
Form Only
|
May 01, 2007
|
FDA
|
3537
a
|
Cancellation of Food Facility Registration
|
Instructions Only
|
May 01, 2007
|
FDA
|
3538
|
Electronic Submission System Participant Password or Addition
|
Both Form and Instructions
|
Jul 01, 2007
|
FDA
|
3540
|
Prior Notice Submission
|
Both Form and Instructions
|
May 01, 2007
|
FDA
|
3541
|
Premarket Notificaiton [510(k)] Status request and Response
|
Form Only
|
Sep 01, 2007
|
FDA
|
3542
a
|
Patent Information Submitted With the Filing of An NDA, Amendment, or Supplement
|
Form Only
|
Jul 01, 2007
|
FDA
|
3542
|
Patent Information Submitted Upon and After Approval of An NDA or Supplement
|
Form Only
|
Jul 01, 2007
|
FDA
|
3546
|
Animal Drug User Fee Cover Sheet
|
Form Only
|
Jun 01, 2008
|
FDA
|
356
v
|
New Animal Drug Application (VET)
|
Form Only
|
Apr 01, 2008
|
FDA
|
356
v
|
New Animal Drug Application (VET)
|
Form Only
|
Dec 01, 2004
|
FDA
|
356
h
|
Application to Market a New Drug, Biologic or an Antibiotic Drug for Human Use
|
Form Only
|
Oct 01, 2005
|
FDA
|
3570
|
Model Small Business Food Labeling Exemption Notice
|
Form Only
|
Feb 01, 2007
|
FDA
|
3571
|
Infusion Pump Information Submission Report
|
Both Form and Instructions
|
Jun 01, 2006
|
FDA
|
3601
|
Medical Device User Fee Cover Sheet
|
Form Only
|
Jan 01, 2007
|
FDA
|
3602
|
FY 2009 MDUFMA Small Business Qualification Certification For a Business Headquartered in the United States
|
Both Form and Instructions
|
Oct 01, 2008
|
FDA
|
3602
a
|
FY 2009 MDUFMA Small Business Qualification Certification For a Business Headquartered Outside the United States
|
Both Form and Instructions
|
Oct 01, 2008
|
FDA
|
3608
|
Medical Device Fellowship Program Student Application
|
Both Form and Instructions
|
Jun 01, 2005
|
FDA
|
3613
a
|
Supplementary Information Certificate of Exportability Requests
|
Form Only
|
Sep 01, 2006
|
FDA
|
3613
d
|
Office of Cosmetics and Colors "Certificate" Export Application
|
Form Only
|
Feb 01, 2006
|
FDA
|
3613
c
|
Supplementary Information Non-Clinical Research Use Only Certificate
|
Form Only
|
Sep 01, 2006
|
FDA
|
3613
|
Supplimentary Information Certificate to Foreign Government Requests
|
Form Only
|
Sep 01, 2006
|
FDA
|
3613
e
|
Food Export Certificate Application
|
Form Only
|
Feb 01, 2006
|
FDA
|
3613
b
|
Supplementary Information Certificate of a Pharmaceutical Product
|
Form Only
|
Jun 01, 2006
|
FDA
|
3626
|
A Guide for the Submission of Initial Reports on Diagnostic X-ray Systems and Their Major Components
|
Form Only
|
Jul 01, 2007
|
FDA
|
3627
|
Diagnostic X-Ray CT Products Radiation Safety Report
|
Form Only
|
Jul 01, 2007
|
FDA
|
3630
|
Guide for Preparing Product Reports on Sunlamps and Sunlamp Products
|
Form Only
|
Jul 01, 2007
|
FDA
|
3631
|
Guide for Preparing Annual Reports on Radiation Safety Testing of Sunlamps and Sunlamp Products
|
Form Only
|
Jul 01, 2007
|
FDA
|
3632
|
Guide for Preparing Product Reports on Lasers and Products Containing Lasers
|
Form Only
|
Jul 01, 2007
|
FDA
|
3634
|
Television Products Annual Report
|
Form Only
|
Jul 01, 2007
|
FDA
|
3636
|
Guide for Preparing Annual Reports on Radiation Safety Testing of Laser and Laser Light Show
|
Form Only
|
Jul 01, 2007
|
FDA
|
3638
|
Guide for Filling Annual Reports for X-Ray Components and Systems
|
Both Form and Instructions
|
Jul 01, 2007
|
FDA
|
3639
|
Guidance for Submission of Cabinet X-Ray System Reports Pursuant to 21 CFR 1020.40
|
Both Form and Instructions
|
Jul 01, 2007
|
FDA
|
3640
|
Reporting Guide for Laser Light Shows and Displays
|
Both Form and Instructions
|
Jul 01, 2007
|
FDA
|
3641
|
Cabinet X-Ray Annual Report
|
Both Form and Instructions
|
Jul 01, 2007
|
FDA
|
3643
|
Microwave Oven Products Annual Report
|
Both Form and Instructions
|
Jul 01, 2007
|
FDA
|
3644
|
Guide for Preparing Product Reports for Ultrasonic Therapy Products
|
Both Form and Instructions
|
Jul 01, 2007
|
FDA
|
3645
|
Guide for Preparing Annual Reports for Ultrasonic Therapy Products
|
Form Only
|
Jul 01, 2007
|
FDA
|
3646
|
Mercury Vapor Lamp Products Radiation Safety Report
|
Form Only
|
Jul 01, 2007
|
FDA
|
3647
|
Guide for Preparing Annual Reports on Radiation Safety Testing of Mercury Vapor Lamps
|
Form Only
|
Jul 01, 2007
|
FDA
|
3654
|
Standards Data Report for 510(K)s
|
Form Only
|
Sep 01, 2007
|
FDA
|
3659
|
Reporting and Compliance Guide for Television Products
|
Form Only
|
Jul 01, 2007
|
FDA
|
3660
|
Guidance for Preparing Reports on Radiation Safety of Microwave Ovens
|
Form Only
|
Jul 01, 2007
|
FDA
|
3661
|
A Guide for the Submission of an Abbreviated Report on X-ray Tables, Cradles, Film Changers or Cassette Holders Intended for Diagnostic Use
|
Form Only
|
Jul 01, 2007
|
FDA
|
3662
|
A A Guide for Submission of an Abbreviated Radiation Safety Reports on Cephalometric Devices Intended for Diagnostic Use
|
Form Only
|
Jul 01, 2007
|
FDA
|
3663
|
Abbreviated Reports on Radiation Safety for Microwave Products (Other than Microwave Ovens)
|
Form Only
|
Jul 01, 2007
|
FDA
|
3670
|
Medical Product Saftey Network
|
Form Only
|
Mar 01, 2008
|
FDA
|
3671
|
Common EMEA/FDA Application for Orphan Medicinal Product Designation
|
Both Form and Instructions
|
Nov 01, 2007
|
FDA
|
766
|
Application for Authorization to Relabel or to Perform Other Action of the Federal Food, Drug,
|
Form Only
|
Dec 01, 2004
|