[Federal Register Volume 90, Number 11 (Friday, January 17, 2025)]
[Notices]
[Pages 5900-5909]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2025-01149]
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DEPARTMENT OF HEALTH AND HUMAN SERVICES
Food and Drug Administration
[Docket No. FDA-2024-N-5468]
Agency Information Collection Activities; Proposed Collection;
Comment Request; Food and Drug Administration's Adverse Event and
Product Experience Reporting Program
AGENCY: Food and Drug Administration, HHS.
ACTION: Notice.
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SUMMARY: The Food and Drug Administration (FDA, the Agency, or we) is
announcing an opportunity for public comment on the proposed collection
of certain information by the Agency. Under the Paperwork Reduction Act
of 1995 (PRA), Federal Agencies are required to publish notice in the
Federal Register concerning each proposed collection of information,
including each proposed extension of an existing collection of
information, and to allow 60 days for public comment in response to the
notice. This notice solicits comments on information collection
associated with FDA's
[[Page 5901]]
adverse event reports and product experience reports for FDA-regulated
products.
DATES: Either electronic or written comments on the collection of
information must be submitted by March 18, 2025.
ADDRESSES: You may submit comments as follows. Please note that late,
untimely filed comments will not be considered. The https://www.regulations.gov electronic filing system will accept comments until
11:59 p.m. Eastern Time at the end of March 18, 2025. Comments received
by mail/hand delivery/courier (for written/paper submissions) will be
considered timely if they are received on or before that date.
Electronic Submissions
Submit electronic comments in the following way:
Federal eRulemaking Portal: https://www.regulations.gov.
Follow the instructions for submitting comments. Comments submitted
electronically, including attachments, to https://www.regulations.gov
will be posted to the docket unchanged. Because your comment will be
made public, you are solely responsible for ensuring that your comment
does not include any confidential information that you or a third party
may not wish to be posted, such as medical information, your or anyone
else's Social Security number, or confidential business information,
such as a manufacturing process. Please note that if you include your
name, contact information, or other information that identifies you in
the body of your comments, that information will be posted on https://www.regulations.gov.
If you want to submit a comment with confidential
information that you do not wish to be made available to the public,
submit the comment as a written/paper submission and in the manner
detailed (see ``Written/Paper Submissions'' and ``Instructions'').
Written/Paper Submissions
Submit written/paper submissions as follows:
Mail/Hand Delivery/Courier (for written/paper
submissions): Dockets Management Staff (HFA-305), Food and Drug
Administration, 5630 Fishers Lane, Rm. 1061, Rockville, MD 20852.
For written/paper comments submitted to the Dockets
Management Staff, FDA will post your comment, as well as any
attachments, except for information submitted, marked and identified,
as confidential, if submitted as detailed in ``Instructions.''
Instructions: All submissions received must include the Docket No.
FDA-2024-N-5468 for ``FDA's Adverse Event and Product Experience
Reporting Program.'' Received comments, those filed in a timely manner
(see ADDRESSES), will be placed in the docket and, except for those
submitted as ``Confidential Submissions,'' publicly viewable at https://www.regulations.gov or at the Dockets Management Staff between 9 a.m.
and 4 p.m., Monday through Friday, 240-402-7500.
Confidential Submissions--To submit a comment with
confidential information that you do not wish to be made publicly
available, submit your comments only as a written/paper submission. You
should submit two copies total. One copy will include the information
you claim to be confidential with a heading or cover note that states
``THIS DOCUMENT CONTAINS CONFIDENTIAL INFORMATION.'' The Agency will
review this copy, including the claimed confidential information, in
its consideration of comments. The second copy, which will have the
claimed confidential information redacted/blacked out, will be
available for public viewing and posted on https://www.regulations.gov.
Submit both copies to the Dockets Management Staff. If you do not wish
your name and contact information to be made publicly available, you
can provide this information on the cover sheet and not in the body of
your comments and you must identify this information as
``confidential.'' Any information marked as ``confidential'' will not
be disclosed except in accordance with 21 CFR 10.20 and other
applicable disclosure law. For more information about FDA's posting of
comments to public dockets, see 80 FR 56469, September 18, 2015, or
access the information at: https://www.govinfo.gov/content/pkg/FR-2015-09-18/pdf/2015-23389.pdf.
Docket: For access to the docket to read background documents or
the electronic and written/paper comments received, go to https://www.regulations.gov and insert the docket number, found in brackets in
the heading of this document, into the ``Search'' box and follow the
prompts and/or go to the Dockets Management Staff, 5630 Fishers Lane,
Rm. 1061, Rockville, MD 20852, 240-402-7500.
FOR FURTHER INFORMATION CONTACT: JonnaLynn Capezzuto, Office of
Operations, Food and Drug Administration, Three White Flint North, 10A-
12M, 11601 Landsdown St., North Bethesda, MD 20852, 301-796-3794,
[email protected].
SUPPLEMENTARY INFORMATION: Under the PRA (44 U.S.C. 3501-3521), Federal
Agencies must obtain approval from the Office of Management and Budget
(OMB) for each collection of information they conduct or sponsor.
``Collection of information'' is defined in 44 U.S.C. 3502(3) and 5 CFR
1320.3(c) and includes Agency requests or requirements that members of
the public submit reports, keep records, or provide information to a
third party. Section 3506(c)(2)(A) of the PRA (44 U.S.C. 3506(c)(2)(A))
requires Federal Agencies to provide a 60-day notice in the Federal
Register concerning each proposed collection of information, including
each proposed extension of an existing collection of information,
before submitting the collection to OMB for approval. To comply with
this requirement, FDA is publishing notice of the proposed collection
of information set forth in this document.
With respect to the following collection of information, FDA
invites comments on these topics: (1) whether the proposed collection
of information is necessary for the proper performance of FDA's
functions, including whether the information will have practical
utility; (2) the accuracy of FDA's estimate of the burden of the
proposed collection of information, including the validity of the
methodology and assumptions used; (3) ways to enhance the quality,
utility, and clarity of the information to be collected; and (4) ways
to minimize the burden of the collection of information on respondents,
including through the use of automated collection techniques, when
appropriate, and other forms of information technology.
FDA's Adverse Event and Product Experience Reporting Program
OMB Control Number 0910-0291--Extension
This information collection supports FDA laws and regulations
governing adverse event reports and product experience reports for FDA-
regulated products. The Federal Food, Drug, and Cosmetic Act (FD&C Act)
(21 U.S.C. 353b, 355, 360i, 360l, 379aa, and 393) and the Public Health
Service Act (42 U.S.C. 262) authorize FDA to collect adverse event
reports and product experience reports from regulated industry and to
monitor the safety of drugs, biologics, medical devices, and dietary
supplements. These reporting and recordkeeping requirements are found
in FDA regulations, discussed in Agency guidance, and included in
Agency forms. Although there are no laws or regulations mandating
postmarket reporting for medical foods, infant formula, cosmetics, or
tobacco products, we encourage voluntary
[[Page 5902]]
reporting of adverse experiences associated with these products.
To facilitate both consumer and industry reporting of adverse
events and experiences with FDA-regulated products, we developed the
MedWatch program. The MedWatch program allows anyone to submit reports
to FDA on adverse events, including injuries and/or deaths, as well as
other product experiences associated with the products we regulate.
Requirements regarding mandatory reporting of adverse events or product
problems have been codified in parts 310, 314, 329, 600, and 803 (21
CFR parts 310, 314, 329, 600, and 803), and specified in sections 503B,
760, and 761 of the FD&C Act (21 U.S.C. 353b, 379aa, and 379aa-1).
Mandatory reporting of adverse events for human cells, tissues, and
cellular- and tissue-based products (HCT/Ps) have been codified in
Sec. 1271.350 (21 CFR 1271.350). Other postmarketing reporting
associated with requirements found in sections 201, 502, 505, and 701
(21 U.S.C. 321, 352, 355, and 371) of the FD&C Act and applicable to
certain drug products with and without approved applications are
approved under OMB control number 0910-0230. Mandatory reporting under
part 803, associated with medical device products, using Form FDA
3500A, is approved under OMB control number 0910-0437.
Since 1993, mandatory adverse event reporting has been supplemented
by voluntary reporting by healthcare professionals, patients, and
consumers via the MedWatch reporting process. To carry out its
responsibilities, the Agency needs to be informed when an adverse
event, product problem, error with use of a human medical product, or
evidence of therapeutic failure is suspected or identified in clinical
use. When FDA receives this information from healthcare professionals,
patients, or consumers, the report becomes data that will be used to
assess and evaluate the risk associated with the product. FDA will take
any necessary action to reduce, mitigate, or eliminate the public's
exposure to the risk through regulatory and public health
interventions.
To implement these reporting provisions for FDA-regulated products
(except vaccines) during their post-approval and marketed lifetimes, we
developed the following three forms, available for download from our
website or upon request to the Agency: (1) Form FDA 3500 may be used
for voluntary (i.e., not mandated by law or regulation) reporting by
healthcare professionals; (2) Form FDA 3500A is used for mandatory
reporting (i.e., required by law or regulation); and (3) Form FDA
3500B, available in English and Spanish, is written in plain language
and may be used for voluntary reporting (i.e., not mandated by law or
regulation) by consumers (i.e., patients and their caregivers).
Respondents to the information collection are healthcare professionals,
medical care organizations and other user facilities (e.g., extended
care facilities, ambulatory surgical centers), consumers, manufacturers
of biologicals, food products including dietary supplements and special
nutritional products (e.g., infant formula and medical foods),
cosmetics, drug products or medical devices, and importers.
I. Use of Form FDA 3500, MedWatch--the Safety Information and Adverse
Event Reporting Program (Voluntary Reporting)
This voluntary version of the form may be used by healthcare
professionals to submit all reports not mandated by Federal law or
regulation. Individual healthcare professionals are not required by law
or regulation to submit reports to the Agency or the manufacturer,
except for certain adverse events following immunization with vaccines
as mandated by the National Childhood Vaccine Injury Act of 1986.
Reports for vaccines are not submitted via MedWatch or MedWatch forms
but are submitted to the Vaccines Adverse Event Reporting System
(VAERS; see http://vaers.hhs.gov), which is jointly administered by FDA
and the Centers for Disease Control and Prevention.
Hospitals are not required by Federal law or regulation to submit
reports associated with drug products, biological products, or special
nutritional products. However, hospitals and other user facilities are
required by Federal law to report medical device-related deaths and
serious injuries (approved under OMB control number 0910-0437).
Under Federal law and regulation (section 761(b)(1) of the FD&C
Act), a dietary supplement manufacturer, packer, or distributor whose
name appears on the label of a dietary supplement marketed in the
United States is required to submit to FDA any serious adverse event
report it receives regarding use of the dietary supplement in the
United States. However, FDA bears the burden to gather and review
evidence that a dietary supplement may be adulterated under section 402
of the FD&C Act (21 U.S.C 342) after that product is marketed.
Therefore, the Agency depends on the voluntary reporting by healthcare
professionals and especially by consumers of suspected serious adverse
events and product quality problems associated with the use of dietary
supplements. All dietary supplement reports were originally received by
the Agency on paper versions of Form FDA 3500 (by mail or fax). Today,
electronic reports may be sent to the Agency via an online submission
route called the Safety Reporting Portal at http://www.safetyreporting.fda.gov/. In that case, the Form FDA 3500 is not
used.
Form FDA 3500 may be used to report to the Agency adverse events,
product problems, product use errors, and therapeutic failures. The
form is provided in both paper and electronic formats. Reporters may
mail or fax forms to the Agency. A fillable PDF version of the form is
available at https://www.accessdata.fda.gov/scripts/medwatch/ or
respondents can electronically submit a report via the MedWatch Online
Voluntary Reporting Form at https://www.accessdata.fda.gov/scripts/medwatch/.
Reporting using Form FDA 3500 in paper form is supported for drugs,
non-vaccine biologicals, medical devices, food products, special
nutritional products, cosmetics, and non-prescription human drug
products marketed without an approved application, and dietary
supplements. Electronic reports for FDA products may be submitted to
the Agency via an online submission route called the Safety Reporting
Portal at http://www.safetyreporting.fda.gov/. Electronic reports for
tobacco products may be submitted to the Agency via the tobacco
questionnaire within the online Safety Reporting Portal at http://www.safetyreporting.fda.gov/.
II. Use of Form FDA 3500A, MedWatch for Use by User-Facilities,
Importers, Distributors, and Manufacturers (Mandatory Reporting)
A. Drug and Biological Products
Sections 503B, 505(j), and 704 of the FD&C Act (21 U.S.C. 374)
require that important safety information relating to all human
prescription drug products be made available to FDA in the event it
becomes necessary to take appropriate action to ensure protection of
the public health. Mandatory reporting of adverse events for HCT/Ps is
codified in Sec. 1271.350. Consistent with statutory requirements,
information is required to be submitted electronically and therefore we
account for most all reports under OMB control number 0910-0230 to
support electronic reporting to our MedWatch program. At the same time,
[[Page 5903]]
regulations are provided for waivers from the electronic submission
requirements and we therefore account for paper-based reporting in this
information collection.
B. Medical Device Products
Section 519 of the FD&C Act (21 U.S.C. 360i) requires manufacturers
and importers of devices intended for human use to establish and
maintain records, make reports, and provide information as the
Secretary of Health and Human Services (the Secretary) may by
regulation reasonably require assuring that such devices are not
adulterated or misbranded and to otherwise assure its safety and
effectiveness. The Safe Medical Device Act of 1990 (Pub. L. 101-629),
signed into law on November 28, 1990, amends section 519 of the FD&C
Act. The amendment requires that user facilities such as hospitals,
nursing homes, ambulatory surgical facilities, and outpatient treatment
facilities report deaths related to medical devices to FDA and to the
manufacturer, if known. Serious illnesses and injuries are to be
reported to the manufacturer or to FDA if the manufacturer is not
known. These statutory requirements regarding mandatory reporting have
been codified by FDA under part 803. Part 803 mandates the use of Form
FDA 3500A for reporting to FDA on medical devices. Mandatory reporting
associated with medical device products using Form FDA 3500A is
approved under OMB control number 0910-0437.
C. Dietary Supplements
Section 502(x) of the FD&C Act implements the requirements of The
Dietary Supplement and Nonprescription Drug Consumer Protection Act,
which became law (Pub. L. 109-462) on December 22, 2006. These
requirements apply to manufacturers, packers, and distributors of
nonprescription human drug products marketed without an approved
application. The law requires reports of serious adverse events to be
submitted to the Agency by manufacturers of dietary supplements.
Electronic reports for dietary supplements may be submitted using
the Safety Reporting Portal at http://www.safetyreporting.fda.gov/.
Paper-based dietary supplement reports may be submitted using the
MedWatch Form FDA 3500A.
III. Use of Form FDA 3500B, MedWatch Consumer Voluntary Reporting
This voluntary version of the form may be used by consumers,
patients, or caregivers to submit reports not mandated by Federal law
or regulation. Individual consumers, patients, or caregivers are not
required by law or regulation to submit reports to the Agency or the
manufacturer. FDA supports and encourages direct reporting to the
Agency by consumers of suspected adverse events and other product
problems associated with human medical products, food, dietary
supplements, and cosmetic products, and invite these respondents to
visit our website at https://www.fda.gov/safety/report-problem-fda for
more information. Since the inception of the MedWatch program in July
1993, the program has been promoting and facilitating voluntary
reporting by both the public and healthcare professionals. FDA has
further encouraged voluntary reporting by requiring inclusion of the
MedWatch toll-free phone number or the MedWatch website on all
outpatient drug prescriptions dispensed, as mandated by section 17 of
the Best Pharmaceuticals for Children Act (Pub. L. 107-109).
Section 906 of the FDA Amendments Act (FDAAA) amended section
502(n) of the FD&C Act, mandating that published direct-to-consumer
advertisements for prescription drugs include the following statement
printed in conspicuous text (this includes vaccine products): ``You are
encouraged to report negative side effects of prescription drugs to the
FDA. Visit https://www.fda.gov/medwatch, or call 1-800-FDA-1088.'' Most
private vendors of consumer medication information, which is the drug
product-specific instructions dispensed to consumers at outpatient
pharmacies, remind patients to report ``side effects'' to FDA and
provide contact information to permit MedWatch reporting.
Form FDA 3500B, first made available in 2013, was tailored for
consumers and has been written in plain language to conform with the
Plain Writing Act of 2010 (Pub. L. 111-274) (https://www.govinfo.gov/content/pkg/PLAW-111publ274/pdf/PLAW-111publ274.pdf), and has evolved
with input from human factors experts, from other regulatory agencies,
and with extensive input from consumer advocacy groups and the public.
It is used to report adverse events, product problems, product use
errors, and problems after switching from one product maker to another
maker to the Agency. The form is available in Spanish at https://www.fda.gov/safety/medwatch-fda-safety-information-and-adverse-event-reporting-program/reporting-serious-problems-fda, and since 2021, has
been available to upload electronically at https://www.accessdata.fda.gov/scripts/medwatch/index.cfm?action=reporting.spanish. The form is provided in both paper
and electronic formats. Respondents may submit reports by mail or fax
to the Agency, or electronically submit a report via the MedWatch
Online Voluntary Reporting Form at https://www.accessdata.fda.gov/scripts/medwatch/. A fillable PDF version of the form, available at
http://www.fda.gov/downloads/AboutFDA/ReportsManualsForms/Forms/UCM349464.pdf, may be downloaded, completed, and mailed or faxed to the
Agency. Reporting is supported for drugs, non-vaccine biologicals,
medical devices, food products, special nutritional products,
cosmetics, and non-prescription human drug products marketed without an
approved application. The paper form may also be used to submit reports
about dietary supplements. Electronic reports for dietary supplements
may be submitted to the Agency via an online submission route called
the Safety Reporting Portal at https://www.safetyreporting.fda.gov/.
IV. Use of Form FDA 3800, Safety Reporting Portal
The Safety Reporting Portal (SRP) streamlines the process of
reporting product safety issues to FDA. Organizations and people in
certain professional roles, such as the following, may be required by
law to submit safety reports under some circumstances: food
manufacturers, processors, packers, and holders; researchers; an
applicant of an approved drug product or a manufacturer; distributor or
packer listed on the label of any marketed drug product; drug
manufacturers, sponsors, sponsor-investigators of investigational drugs
and biologics; dietary supplement manufacturers, packers, and
distributors; and tobacco product manufacturers.
Others, including healthcare providers, public health officials,
and other professionals, as well as consumers and concerned citizens,
may voluntarily submit reports if they encounter safety issues with a
product and/or harmful effects that they believe are related to a
product. The information collection includes the following Agency
forms, available electronically, via the Safety Reporting Portal:
Center for Veterinary Medicine (CVM)--Voluntary reporting
of adverse events and product problems involving pet food or livestock
food. Section 1002(b) of the FDAAA directed the Secretary to establish
an early warning and surveillance system to identify
[[Page 5904]]
adulteration of the pet food supply and outbreaks of illness associated
with pet food. We developed the Pet Food Early Warning System rational
questionnaire as a user-friendly data collection tool, as well as a
questionnaire for collecting voluntary adverse event reports associated
with pet and livestock food. Information collected in these voluntary
adverse event reports contribute to CVM's ability to identify
adulteration of the pet and livestock food supply and outbreaks of
illness associated with pet and livestock food. We use the information
collected to help ensure that such products are quickly and efficiently
removed from the market to prevent foodborne illnesses.
Center for Tobacco Products (CTP)--Voluntary Tobacco
Product Health Problem or Product Problem Reports (i.e., Adverse
experience reports). Voluntary adverse experience reports have been
collected from consumers/concerned citizens and healthcare
professionals via the SRP's Tobacco Problem Report (TPR) questionnaire
since January 10, 2014, from tobacco product manufacturers via the SRP
TPR since June 10, 2016, and from researchers engaged in clinical
trials using investigational or legally marketed tobacco products via
the SRP Tobacco Investigator Report (TIR) questionnaire since June 10,
2016.
CTP--Mandatory Tobacco Product Health Problem or Product
Problem Reports (i.e., Adverse experience reports). On October 5, 2021
(86 FR 55300), FDA published a final rule entitled ``Premarket Tobacco
Product Applications and Recordkeeping Requirements.'' The rule
establishes regulatory definitions (21 CFR 1114.3) for adverse
experience, serious adverse experience, and unexpected adverse
experience associated with tobacco product use. The final rule, in
effect since November 4, 2021, requires premarket applicants
(manufacturers of new tobacco products) who receive marketing granted
orders to report all serious and unexpected adverse experiences
associated with the tobacco product (21 CFR 1114.41(a)(2)) that have
been reported to the applicant or of which the applicant is aware, to
the SRP or in another manner designated by FDA, within 15 calendar days
of their awareness.
V. Proposed Modifications to Existing Forms 3500, 3500A, and 3500B
A. General Changes
The proposed modifications to Form FDA 3500, Form FDA 3500A, and
Form FDA 3500B (English and Spanish) reflect changes that will bring
the forms into conformity, since the previous authorization in 2022,
with current regulations, rules, and guidances. The proposed extension
to Form FDA 3500, Form FDA 3500A, and Form FDA 3500B will only have
changes in the form instructions to provide clarity of reporting. The
proposed changes fall into one of three categories: (1) regulatory
driven revisions, (2) work improvements for the Center, and (3) report
processing improvements. Formatting modifications are being proposed to
several fields to enhance the quality, utility, and clarity of the
information. We also propose to update the mailing address to Attn:
MedWatch Program, White Oak Campus, Building 22, G0207, 10903 New
Hampshire Ave., Silver Spring, MD 20993.
B. Changes Proposed for Form FDA 3500
Throughout the form, we propose to add calendar functionality to
all date fields for uniformity and standardization of date format.
In the header, we propose to specify the intended reporters at the
top of the form (i.e., Health Professional Voluntary Reporting). In
section A, we propose to revise ``Undifferentiated'' to ``Intersex'' in
field 3a; combine the ``Ethnicity'' (field A5) and ``Race'' (field A6)
fields as outlined in the Statistical Policy Directive No. 15:
Standards for Maintaining, Collecting, and Presenting Federal Data on
Race and Ethnicity (SPD 15) issued on March 29, 2024; and add new text
``What is your race and/or ethnicity? Select all that apply.''
The selections will also include descriptions of each category. The
data fields include the following:
American Indian or Alaska Native--For example, Navajo
Nation, Blackfeet Tribe of the Blackfeet Indian Reservation of Montana,
Native Village of Barrow Inupiat Traditional Government, Nome Eskimo
Community, Aztec, Maya, etc.
Asian--For example, Chinese, Asian Indian, Filipino,
Vietnamese, Korean, Japanese, etc.
Black or African American--For example, African American,
Jamaican, Haitian, Nigerian, Ethiopian, Somali, etc.
Hispanic or Latino--For example, Mexican, Puerto Rican,
Salvadoran, Cuban, Dominican, Guatemalan, etc.
Middle Eastern or North African--For example, Lebanese,
Iranian, Egyptian, Syrian, Iraqi, Israeli, etc.
Native Hawaiian or Pacific Islander--For example, Native
Hawaiian, Samoan, Chamorro, Tongan, Fijian, Marshallese, etc.
White--For example, English, German, Irish, Italian,
Polish, Scottish, etc.
In section B, we propose to reorder the outcomes attributed to the
adverse events list so that ``Other Serious or Important Medical
Events'' appears as the last choice of the outcomes listed in field B2,
and add a field for reference ranges in the ``Relevant Test/Laboratory
Data'' section (field B6).
In section C, we propose to add a field for ``Where (e.g., website,
pharmacy/store/state of purchase) was the suspect product obtained?''
and ``When (date) was the suspect product obtained?''
In section D, we propose to remove ``This report involves cosmetic,
dietary supplement, food/medical food, and other.'' Cosmetic will now
be captured under the ``Product Type'' section field D5.
We propose to add ``Usage Dates'' after ``Treatment Dates/Therapy
Dates'' and add ``Usage'' after ``Treatment'' and ``Therapy'' in field
D3. We propose to revise the ``Product Type'' section (field D5) as
follows: (Dietary supplement and Food/medical food selections will be
removed. Adverse events involving these products should be submitted
through the Safety Reporting Portal)
[cir] Drug or Biologic
[squf] Brand
[squf] Generic or Biosimilar
[squf] Over-the Counter (OTC)
[squf] Compounded product (by a Pharmacy or an Outsourcing
Facility)
[cir] Cosmetic
[squf] Cosmetic for professional use only
[squf] Cosmetic sold on a retail basis
[cir] Cannabinoid Hemp Products (such as products containing CBD)
[cir] Other
In section E, we propose to interchange the fields 2a and 2b so
that ``Procode'' will now appear in field 2a and ``Common Device Name''
will appear in field 2b.
In section G, we propose to add a field entitled ``Packer'' to the
list under ``Also Reported To'' in field G4.
In the ``Advice about Voluntary Reporting'' section, we propose to
remove ``Special nutritional products (dietary supplements, medical
foods, infant formulas)'' and ``Food (including beverages and
ingredients added to foods'' and add ``If your report involves a health
problem or product problem with foods or special nutritional products
such as infant formulas, dietary supplements, or medical foods'', go to
https://www.safetyreporting.fda.gov or call 1-888-723-3366 to report.
We propose to revise ``If your report involves a health problem or
a product
[[Page 5905]]
problem with a tobacco product, go to https://www.safetyreporting.fda.gov or call 1-877-287-1363 to report.'' to ``If
your report involves a health problem or a product problem with a
tobacco product, including e-cigarettes (nicotine-containing vapes) or
nicotine pouches, go to https://www.safetyreporting.fda.gov or call 1-
877-287-1363 to report.''
C. Changes Proposed for Form FDA 3500A
Throughout the form, we propose to add calendar functionality to
all date fields for uniformity and standardization of date format.
In the header, we propose to revise ``For use by user-facilities,
importers, distributors and manufacturers'' to ``For use by user-
facilities, importers, distributors, manufacturers and packers.'' We
propose to remove the header ``FDA USE ONLY'' and revise the
``Exemption/Variance #'' field to ``Exemption/Variance/Alternative #.''
In section A, we propose to revise ``Undifferentiated'' to
``Intersex'' in field 3, combine the ``Ethnicity'' (field A5) and
``Race'' (field A6) fields as outlined in the Statistical Policy
Directive No. 15: Standards for Maintaining, Collecting, and Presenting
Federal Data on Race and Ethnicity (SPD 15) issued on March 29, 2024,
and propose to add the new text ``What is your race and/or ethnicity?
Select all that apply.'' The selections will also include descriptions
of each category.
The data fields include the following: combine the ``Ethnicity''
(field A5) and ``Race'' (field A6) fields as outlined in the
Statistical Policy Directive No. 15: Standards for Maintaining,
Collecting, and Presenting Federal Data on Race and Ethnicity (SPD 15)
issued on March 29, 2024 and add ``What is your race and/or ethnicity?
Select all that apply.'' The selections will also include descriptions
of each category.
The data fields include:
American Indian or Alaska Native--For example, Navajo
Nation, Blackfeet Tribe of the Blackfeet Indian Reservation of Montana,
Native Village of Barrow Inupiat Traditional Government, Nome Eskimo
Community, Aztec, Maya, etc.
Asian--For example, Chinese, Asian Indian, Filipino,
Vietnamese, Korean, Japanese, etc.
Black or African American--For example, African American,
Jamaican, Haitian, Nigerian, Ethiopian, Somali, etc.
Hispanic or Latino--For example, Mexican, Puerto Rican,
Salvadoran, Cuban, Dominican, Guatemalan, etc.
Middle Eastern or North African--For example, Lebanese,
Iranian, Egyptian, Syrian, Iraqi, Israeli, etc.
Native Hawaiian or Pacific Islander--For example, Native
Hawaiian, Samoan, Chamorro, Tongan, Fijian, Marshallese, etc.
White--For example, English, German, Irish, Italian,
Polish, Scottish, etc.
In section B, we propose to reorder the outcomes attributed to
adverse events list so that ``Other Serious or Important Medical
Events'' appears as the last choice of the outcomes listed in field B2,
add ``Describe Event or Problem'' on page 1 and add ``Describe Event or
Problem (continued)'' on page 2 (field B5), and add a field for
reference ranges in the ``Relevant Test/Laboratory Data'' section
(field B6)
In section C, we propose to revise the ``Name, Strength,
Manufacturer/Compounder'' field under ``Manufacturer/Compounder Name''
to include a new field for ``FEI # for cosmetics''. This revision
applies to ``Suspect Product #1'' and ``Suspect Product #2.'' (field
C1). We propose to revise ``Usage Dates'' after ``Treatment Dates/
Therapy Dates'' and add ``Usage'' after ``Treatment'' and ``Therapy.''
(field C4).
We propose to revise the ``Product Type'' section (field C6) as
follows (applies to Suspect Product #1 and Suspect Product #2):
[cir] Drug or Biologic
[squf] Brand
[squf] Generic or Biosimilar
[squf] Over-the Counter (OTC)
[squf] Compounded product (by a Pharmacy or an Outsourcing
Facility)
[cir] Cosmetic
[squf] Cosmetic for professional use only
[squf] Cosmetic sold on a retail basis
[cir] Other
In section D, we propose to interchange fields 2a and 2b.
``Procode'' will now appear in field 2a and ``Common Device Name'' will
appear in field 2b.
In section F, we propose to revise the ``User Facility or Importer
Name/Address'' field to ``User Facility or Importer Name/Address/
Email'' (field F3), add the two selections ``Initial'' and ``Follow-up
#____.'' with checkboxes in the ``Type of Report'' field (field F7),
and delete the ``Date of This Report (01-JAN-1900)'' field (field F8).
This information is requested in ``Report Sent to FDA?'' (field F11) or
``Report Sent to Manufacturer?'' (field F13).
In section G, we propose to revise ``Contact Office (and
Manufacturing Site for Devices)'' or ``Compounding Outsourcing
Facility'' to ``Contact Office (and Manufacturing Site for Devices)''
or ``Compounding Outsourcing Facility or Responsible Person'' (field
G1), revise ``Use Facility'' to ``User Facility'' in the ``Report
Source'' field (field G2), revise ``Date Received by Manufacturer (01-
JAN-1900)'' to ``Date Received by Manufacturer (01-JAN-1900)'' or
``Responsible Person'' (field G3), revise ``ANDA #'' to ``ANDA/Pre-ANDA
#.'' (field G4), revise ``Periodic'' to ``Non-expedited (periodic)''
under ``Type of Report'' field (field G6), and revise ``If action
reported to FDA under 21 U.S.C. 360i(g), list correction/removal
reporting number:'' to ``If action reported to FDA under 21 U.S.C.
360i(g), list FDA-assigned recall number or include a statement.''
(field H9)
VI. Changes Proposed for Form FDA 3500A Instructional Supplement
The FDA Form 3500A instructional supplement will be revised to
correct grammatical errors and to clarify reporting instructions. In
addition to these changes, the FDA Form 3500A instructional supplement
will include revisions based on the Modernization of Cosmetics
Registration Act of 2022.
A. General Instructions
The instructional supplement will include the following revisions
specifically pertaining to cosmetics:
Add ``or cosmetic product'' to ``If no suspect medical
device is involved in a reported adverse event (i.e., when reporting
ONLY a suspect drug or, biologic) ONLY sections A, B, C, E, and G are
to be filled out'';
Remove ``or'' between drug and biologic;
Add ``When reporting ONLY a cosmetic product, the sections
and/or subsections/blocks that are not relevant to cosmetics should be
left blank.'';
Add ``Cosmetic Products: Responsible persons submitting
serious adverse event reports for cosmetic products using Form FDA
3500A should include a copy of the label on or within the retail
packaging of the cosmetic product, along with any information that can
be provided to support the report, such as scans of labels and images
of the serious adverse event. This may be submitted to FDA:'';
Add ``via email at: [email protected]''; and
Add ``Or by mail to: FDA CDER Mail Center, Attn: Cosmetics
MedWatch Reports. White Oak Campus, Building 22, G0207, 10903 New
Hampshire Ave., Silver Spring, MD 20993''.
[[Page 5906]]
B. Front Page
For the front page, there are the following revisions:
Add ``For cosmetic products, the User Facility/Importer
Report # and Exemption/Variance # should be left blank in this
section.'';
Add ``(mfr report #): after ``Manufacturer report #'';
Revise ``The manufacturer report number is also entered in
block G9 on the back of the form'' to ``The manufacturer report number
is also entered in block G8 on the back of the form.'';
Add ``and for responsible persons for cosmetic products:''
to ``For drug and biologics manufacturers''; and
Add ``that'' and ``or the responsible person to ``The
``mfr report #'' is the number the manufacturer chooses to uniquely
identify the report, and should conform to any applicable regulations
or guidances.''
C. Section B: Adverse Event or Product Problem
In section ``B1: Type of Report'' adverse event, include ``or
cosmetic product'' to ``Any incident where the use of a product (drug
or biologic, including human cell, tissue, or cellular or tissue-based
product (HCT/P), at any dose, or a medical device (including in vitro
diagnostic products), is suspected to have resulted in an adverse
outcome in a patient.''
In section ``B2: Outcomes attributed to adverse event'', add ``and
Cosmetic Products'' to'' Drugs and Biologics'', and include the
regulatory reference ``21 CFR and section 605 of the FD&C Act,
respectively.''
Under ``Disability or Permanent Damage,'' add ``or cosmetic
products: Check if the adverse event resulted in a persistent or
significant disability or incapacity.''
Under ``Congenital Anomaly/Birth Defect,'' remove ``medical.''
Under ``Other Serious (Important Medical Events),'' add ``Cosmetic
Products: Check if the other categories are not applicable, such as
when the adverse event results in an infection or significant
disfigurement (including serious and persistent rashes, second- or
third-degree burns, significant hair loss, or persistent or significant
alteration of appearance) other than as intended, under conditions of
use that are customary or usual. Describe the outcomes in the actual
narrative of the event in block B5.''
In section ``B4: Date of this Report,'' add ``, and cosmetic
products'' to ``For all mandatory reports filed for Medical Devices,
Drugs, and Biologics, including human cells, tissues, and cellular and
tissue-based products, enter the date the report is submitted to the
FDA.''
In section ``B5: Describe Event or Problem,'' add ``For cosmetics,
please indicate whether the product was for professional use only;
describe the amount and frequency used; for which body parts the
cosmetic product was used; and outcomes.''
D. Section C: Suspect Product(s)
In section ``C: Suspect Product (s),'' add ``For cosmetic products,
fill out ONLY the blocks that are relevant to cosmetic products.''
In subsection C1, add the following after the ``Name, Strength,
Manufacturer/Compounder'' instruction: ``For cosmetics: In the product
name field, enter the statement of identity as such name appears on the
label. If the product names in the listing are not unique, then also
include distinguishing information for identification purposes. For
example, please include a brand name or a code that the responsible
person uses to distinguish the product. Such information may also be
included, in addition to the product name, even when product names in
the listing are unique. If you believe certain distinguishing
information is confidential, please include that distinguishing
information in parentheses.''
In subsection C1, add after the ``NDC# or Unique ID'' instruction:
``For cosmetic product(s), if available, the FDA Establishment
Identifier (FEI) number obtained by the owner or operator of a
facility(ies), of the facility that manufactured or processed the
affected cosmetic product(s). FEI is also known as the Firm or Facility
Establishment Identifier.''
In section ``C2: List Medical Products and Treatment Given at the
Same time of the Event and Date,'' add ``For cosmetic reports include
all related cosmetic products used at the same time.''
In section ``C3: Dose, Frequency & Route Used,'' add ``or the
consumer'' after ``Describe how the product was used by the patient''
and add ``or number of applications, area of application'' in the
parentheses after ``(e.g., 500 mg QID orally or 10 mg every other day
IV).''
In section ``C4: Treatment/Therapy Start and Stop Dates,'' add
``Usage'' to the ``C4: Treatment/Therapy Start and Stop Dates''
heading, and add ``treatment/therapy'' and ``or usage'' to the
following sentence: ``Provide the date of administration was started
(or best estimate) and the date stopped (or best estimate).''
In section C6, add ``Cosmetics for Professional Use Only, Cosmetics
Sold on a Retail Basis,'' after ``Biosimilar,'' and before ``please
check the best option that best fits this medical product.''
In section C7, add ``For cosmetic products, if available, include
best by/use by date'' to the ``Expiration date'' after the current
instruction.
E. Section G: All Manufacturers
In section G, add ``AND RESPONSIBLE PERSONS'' to the ``SECTION G:
ALL MANUFACTURERS'' heading, ``or responsible persons (in case of
cosmetic products)'' to the sentence, ``This section is to be filled
out by all manufacturers,'' ``or cosmetic product'' to ``NOTE: If a
drug, biologic, including human cell, tissue, and cellular and tissue-
based product (HCT/P),'' and ``(or responsible person in case of
cosmetic product)'' to the ``manufacturer is reporting an adverse event
in which no suspect medical device is involved, section G may be
identically reproduced in place of section D on the front of the form
so that a one-page form may be submitted.'' Also add ``For cosmetic
products, fill out ONLY the blocks that are relevant to cosmetic
products.''
In section, ``G1: Contact Office (and manufacturing site for
devices) or Compounding Outsourcing Facility,'' add ``or Responsible
Person (in case of cosmetic products)'' to ``Contact Office (and
manufacturing site for devices) or Compounding Outsourcing Facility''
heading and add ``For cosmetic products, enter the information of the
responsible person, which means the manufacturer, packer, or
distributor of a cosmetic product whose name appears on the label of
the cosmetic product'' to the last sentence
In section ``G2: Report Source,'' add ``and Cosmetic Products'' to
the sentence ``Drugs and Biologics, including HCT/Ps: a separate 3500A
form must be completed for each identifiable patient described in the
article or manuscript.'' Remove the text ``, and'' between ``Drugs and
Biologics.''
In section ``G3: Date received by manufacturer,'' add ``or
responsible person (in case of cosmetic product)'' to the heading and
add ``responsible person,'' to the following sentence: ``This means the
date when the applicant, manufacturer, corporate affiliate, etc.
receives information that an adverse event or medical device
malfunction has occurred.''
In section G6: Type of Report under ``15-day,'' add the following:
``, and cosmetic products'' to ``As specified in
[[Page 5907]]
the drug, biologic, including human cell, tissue, and cellular and
tissue-based product (HCT/P),'' ``or requirements'' to ``regulations
for reports of serious and unexpected adverse events,'' change the
``Periodic'' label to ``Non-expedited (Periodic);'' and add ``For
Cosmetic products, use this option for non-serious adverse event.''
Under Follow-up, add ``and cosmetic products'' to ``Follow-up
reports on drugs, biologics, including HCT/Ps, should contain
information that was submitted in the original report if the
information is still correct.''
In section ``G7: Adverse Event Term(s),'' add ``, and cosmetic
products'' to ``[for use by drug, biologic, including human cell,
tissue, and cellular and tissue-based product (HCT/P),'' add ``(or
responsible persons, in case of cosmetic products)'' to ``manufacturers
only]''and remove ``or WHOART'' from the list of accepted standards.
In ``G8: Manufacturer Report Number,'' remove ``If submitting a
follow-up to a report originally obtained from FDA through a MedWatch
to Manufacturer program transmission of a serious direct report, check
the `Other' box in block G2 and enter the FDA-assigned report number
there'' and add ``For cosmetics: The manufacturer report number is the
number the responsible person chooses to uniquely identify the report,
and should conform to any applicable regulations or guidances. The
submission will not be considered complete without this information.
While FDA currently does not have a mandatory format for the
Manufacturer Report Number for reporting cosmetic adverse events, we
strongly encourage you to use a numbering system that provides unique
information of the adverse event reported, such as the year, company
name, and the case report number.''
VII. Changes Proposed for Form FDA 3500B
In the instructions section, we propose to make the following
revisions:
Under ``When do I use this form?'', revise the first
bullet to ``You were hurt or had a bad side effect (including new or
worsening symptoms) after taking a drug or using a medical device or
product'' to ``You were hurt or had a bad side effect (including new or
worsening symptoms) after using a product, drug, cosmetic or a medical
device.''; and
Add the word ``cosmetic'' after the word ``drug'' in the
following bullets: ``You used a product, drug, cosmetic, or medical
device incorrectly which could have or led to unsafe use'' and ``You
noticed a problem with the quality of the product, drug, cosmetic, or
medical device.''
Under ``Don't use this form to report:'', add the hyperlink for the
Vaccine Adverse Event Reporting System, add descriptive language under
tobacco products about e-cigarettes and nicotine pouches, remove the
word cosmetic from the safety reporting portal language, and revise the
hyperlink to the SRP. Also, add the following:
[cir] Vaccines--report problems to the Vaccine Adverse Event
Reporting System (VAERS) http://vaers.hhs.gov.
[cir] Tobacco products, including e-cigarettes (nicotine-containing
vapes) and nicotine pouches, report health or product problems to the
Safety Reporting Portal (SRP) https://www.safetyreporting.fda.gov/ or
call 1-877-287-1363.
[cir] Remove the word ``cosmetic'' from the last bullet--Food or
dietary supplement products--report problems to the SRP https://www.safetyreporting.fda.gov/.
Under ``What types of products should I use this form for?'', add a
comma between ``bone), allergenics'' in the first bullet, remove
``makeup'' in the third bullet, add a bullet for ``Cannabinoid Hemp
Products (such as products containing CBD'', and remove the last bullet
``Foods (including beverages and ingredients added to foods).
Under ``Are there specific instructions for filling out the
form?'', the first two bullets in this section will remain unchanged
and new text will be added for the third and fourth bullets to read as
follows:
[squf] Including or attaching images of all sides of the product
will help FDA review your report but is not required. Please do not
send the products to FDA.
[squf] The Global Unique Device Identification Database (GUDID)
contains key device identification information submitted to FDA about
medical devices that have Unique Device Identifiers (UDI). In
collaboration with the National Library of Medicine, FDA has created a
portal, called Access GUDID, to make device identification information
in the GUDID available for everyone. For more information regarding the
UDI#, refer to the UDI web page, https://www.fda.gov/medical-devices/device-advice-comprehensive-regulatory-assistance/unique-device-identification-system-udi-system.
Under ``How can I contact the FDA if I have questions?'' add a
following toll-free phone number for cosmetics: 1-888-723-3366, and add
the following language to match that of the MedWatch Online
application: ``If this is a medical emergency, please call 911'' and
``If you have a mental health crisis, please call 988.''
In section ``A--About the Problem,'' we propose to add a field for
reference ranges in the ``Relevant Test/Laboratory Data'' section
(field A5).
In section ``B--Product Availability,'' we propose to revise the
question in field B2 from ``Do you have a picture of the product?
(check yes if you are including a picture)'' to ``Do you have a picture
of the product including product labels if reporting cosmetics? While
not required, pictures of all sides of the product will help FDA review
your report. (check yes if you are including pictures).''
Under the section, ``For a problem with a product, including,''
remove ``or make-up products'' from the fourth bullet and remove the
following bullets 3 and 5: ``nutrition products, such as vitamins and
minerals, herbal remedies, infant formulas, and medical food'' and
``foods (including beverages and ingredients added to foods).
Under the section ``For a health or product problem with a food,
cosmetic, dietary supplement or tobacco product,'' remove the word
``cosmetic'' and revise the hyperlink to the SRP to https://www.safetyreporting.fda.gov/.
In section ``C: About the Products,'' we propose to remove ``This
report is about,'' or field ``C1. Product'' field will be updated, and
add a section for a second suspect product and design the two sections
for suspect product on the same page to facilitate the addition of
another page if the reporter needs to report more than two products.
For field C3, we propose to add ``usage'' after ``therapy.'' The
revised language will be ``Check if therapy/usage is on-going.''
We propose to revise the field ``Product Type'' (field C5) as
follows: ``(Note: Dietary supplement and Food/Medical Food selections
will be removed. Adverse events involving these products should be
submitted through the Safety Reporting Portal)
[cir] Drug or Biologic
[squf] Brand
[squf] Generic or Biosimilar
[squf] Over-the Counter (OTC)
[squf] Compounded product (by a Pharmacy or an Outsourcing
Facility)
[cir] Cosmetic
[squf] Cosmetic for professional use only
[squf] Cosmetic sold on a retail basis
[cir] Cannabinoid Hemp Products (such as products containing CBD
[cir] Other
For field C12, revise instructions from ``How was it taken or used
(for example,
[[Page 5908]]
by mouth, injection, or on the skin)?'' to ``How was it taken or used
(for example, by mouth, injection, inhaled, or on the skin)?'', add a
field for ``Purchase Date'', and add a field for ``Where (e.g.,
website, pharmacy/store/state of purchase) was the suspect product
obtained?'' and ``When (date) was the suspect product obtained?'' We
propose addition of fields to capture ``Place of Purchase Name,'' ``web
page/URL (if purchased online),'' and ``Place of Purchase City and
State/Province.''
Under section ``D--About the Medical Device,'' we propose to add
text to read as ``Unique Device Identifier (UDI) number--Please record
all symbols, letters and numbers located under the barcode. An example
of a UDI number can be found at https://accessgudid.nlm.nih.gov/about-gudid#what-is-udi'' for field D7.
Under section ``E--About the Person Who Had the Problem,'' we
propose to revise ``Undifferentiated'' to ``Intersex'' in field 2a, add
calendar functionality to field E4 (Date of Birth) for uniformity in
reporting and to ensure correct reporting of date format, and combine
the ``Ethnicity'' (field E6) and ``Race'' (field E7) fields as outlined
in the Statistical Policy Directive No. 15: Standards for Maintaining,
Collecting, and Presenting Federal Data on Race and Ethnicity (SPD 15)
issued on March 29, 2024. We propose to add new text ``What is your
race and/or ethnicity? Select all that apply.'' The selections will
also include descriptions of each category.''
The data fields include:
American Indian or Alaska Native--For example, Navajo
Nation, Blackfeet Tribe of the Blackfeet Indian Reservation of Montana,
Native Village of Barrow Inupiat Traditional Government, Nome Eskimo
Community, Aztec, Maya, etc.
Asian--For example, Chinese, Asian Indian, Filipino,
Vietnamese, Korean, Japanese, etc.
Black or African American--For example, African American,
Jamaican, Haitian, Nigerian, Ethiopian, Somali, etc.
Hispanic or Latino--For example, Mexican, Puerto Rican,
Salvadoran, Cuban, Dominican, Guatemalan, etc.
Middle Eastern or North African--For example, Lebanese,
Iranian, Egyptian, Syrian, Iraqi, Israeli, etc.
Native Hawaiian or Pacific Islander--For example, Native
Hawaiian, Samoan, Chamorro, Tongan, Fijian, Marshallese, etc.
White--For example, English, German, Irish, Italian,
Polish, Scottish, etc.
Under section F, ``About the Person Filling Out This Form,'' we
propose to change the title of the field from ``City and State/
Province'' to ``City and State/Province (including your State/Province
will help FDA review your report) for field F4, and under ``Send This
Report by mail or fax,'' revise the mailing address to the following:
Attn: MedWatch Program, White Oak Campus, Building 22, G0207, 10903 New
Hampshire Ave., Silver Spring, MD 20993.
FDA welcomes comments from the public and interested parties on a
proposed report concept.
VIII. Consumer Complaint Form
The consumer complaint form will be used by all Centers to
facilitate reporting complaints and product problems from the public to
FDA. The four required data elements (patient identifier, description
of event or problem, product name, and reporter), demographic
information, and contact information (phone number and/or email
address) may be requested. This form will be available externally with
the long-term goal to allow submission of streamlined reports online.
FDA estimates the burden of this collection of information as
follows:
Table 1--Estimated Annual Reporting Burden \1\
----------------------------------------------------------------------------------------------------------------
Number of
FDA center or 21 CFR section and/ Number of responses per Total annual Average burden Total hours
or FDA form respondents respondent responses per response
----------------------------------------------------------------------------------------------------------------
CBER/CDER, FDA 3500 (voluntary 58,711 1 58,711 0.66 38,749
reporting)..................... (40 minutes)
CBER, FDA 3500A; 600.80; 599 98 58,702 1.21 71,029
1271.350 (mandatory reporting).
CBER, FDA 3500B................. 13,750 1 13,750 0.46 6,325
(28 minutes)
CDER, FDA 3500B................. 18,961 1 18,961 0.46 8,722
(28 minutes)
CDRH, FDA 3500 and FDA 3500B.... 15,304 1 15,304 0.46 7,040
(28 minutes)
CTP, FDA 3500................... 39 1 39 0.66 26
(40 minutes)
HFP, FDA 3500................... 7,442 1.061 7,895 0.66 5,211
(40 minutes)
HFP, FDA 3500A.................. 1,659 1 1,659 1.21 2,007
Written requests for temporary 1 1 1 1 1
waiver under Sec.
329.100(c)(2)..................
-------------------------------------------------------------------------------
Total....................... .............. .............. .............. .............. 139,110
----------------------------------------------------------------------------------------------------------------
\1\ There are no capital costs or operating and maintenance costs associated with this collection of
information.
CBER = Center for Biologics Evaluation and Research
CDER = Center for Drug Evaluation and Research
CDRH = Center for Devices and Radiological Health
HFP = Human Foods Program
CTP = Center for Tobacco Products
The estimates in table 1 are based on current Agency data and our
experience with the information collection.
[[Page 5909]]
Table 2--Estimated Annual Reporting Burden E-Submissions Including via SRP \1\
----------------------------------------------------------------------------------------------------------------
Number of
FDA form 3800 Number of responses per Total annual Average burden Total hours
respondents respondent responses per response
----------------------------------------------------------------------------------------------------------------
Reportable Foods Registry 875 1 875 0.6 (36 525
(mandatory reports)............ minutes)
Reportable Foods Registry 5 1 5 0.6 (36 3
(voluntary reports)............ minutes)
Food, Infant Formula, and 1,165 1.2 1,398 0.6 (36 839
Cosmetic Adverse Event Reports. minutes)
Voluntary Dietary Supplement 360 1.2 432 0.6 (36 259
Adverse Event Reports.......... minutes)
Mandatory Dietary Supplement 80 12 960 1 960
Adverse Event Reports..........
Animal Food: Voluntary Pet Food 1,401 1 1,401 0.6 (36 841
Reports........................ minutes)
Animal Food: Voluntary Livestock 23 1 23 0.6 (36 14
Food Reports................... minutes)
Voluntary Tobacco Product Health 176 1 176 0.6 (36 106
Problem or Product Problem minutes)
(i.e., adverse experience)
Reports to SRP (both
questionnaires)................
Mandatory Tobacco Product Health 3 6 18 0.6 (36 11
Problem or Product Problem minutes)
(i.e., adverse experience)
Reports 1114.41(a)(2)..........
-------------------------------------------------------------------------------
Total....................... .............. .............. 5,924 .............. 3,961
----------------------------------------------------------------------------------------------------------------
\1\ There are no capital costs or operating and maintenance costs associated with this collection of
information.
The number of respondents for the Voluntary Tobacco Product Health
Problem or Product Problem Reports e-submissions has decreased from 204
to 176, according to an updated analysis.
Based on burden estimates associated with the Premarket Tobacco
Product applications and Recordkeeping Requirements regulation, we have
decreased the average burden per response from 1 hour to 36 minutes for
``1114.41(a)(2); Mandatory Tobacco Product Health Problem or Product
Problem Reports.''
CVM reports a decrease in the number of submissions received over
the last few years.
FDA's Center for Drug Evaluation and Research (CDER) and Center for
Biologics Evaluation and Research (CBER) has increased the number of
direct safety reports from healthcare providers and consumers.
Additionally, CDER mandatory reports Form FDA 3500A previously included
in this information collection, are now reported in the approved
information collection, OMB control number 0910-0230. However,
increases in receipts of CBER mandatory reports have obscured any
decrease in burden. Adverse event reports related to 21 CFR 310.305
from outsourcing facilities are also included in OMB control number
0910-0230 and decreases the total burden of this collection.
Based on updated data, the Center for Devices and Radiological
Health (CDRH) has revised our estimate for forms FDA 3500 and FDA
3500B. Additionally, we have determined that the estimate previously
reported in this information collection for mandatory reporting under
part 803, associated with medical device products, using Form FDA
3500A, is redundant with our approved burden estimates in OMB control
number 0910-0437 ``Medical Device Reporting (under part 803).'' We have
therefore removed CDRH reporting via Form FDA 3500A from this
information collection request and continue to account for its burden
in OMB control number 0910-0437.
Based on Agency experience the Human Food Program's estimated
burden for the information collection reflects an overall increase. We
attribute this adjustment to an increase in the number of submissions
we received over the last few years, due primarily to changes in the
infant formula industry.
Therefore, the cumulative changes, both program changes which
include form revisions, and adjustments reflecting fluctuations in
submissions, as well as removing double-counted burden reflects and
overall increase of 116,014 hours to the total burden for this
information collection.
Dated: January 7, 2025.
P. Ritu Nalubola,
Associate Commissioner for Policy.
[FR Doc. 2025-01149 Filed 1-16-25; 8:45 am]
BILLING CODE 4164-01-P