Agency Information Collection Activities; Submission for Office of Management and Budget Review; Comment Request; Aluminum in Large and Small Volume Parenterals Used in Total Parenteral Nutrition, 30143-30144 [E6-7984]
Download as PDF
Federal Register / Vol. 71, No. 101 / Thursday, May 25, 2006 / Notices
ongoing investigation for a drug or
biologic. An applicant may respond to
a clinical hold.
Under section 505(i)(3)(C) of the
Federal Food, Drug, and Cosmetic Act
(21 U.S.C. 355), any written request to
FDA from the sponsor of an
investigation that a clinical hold be
removed must receive a decision, in
writing and specifying the reasons,
within 30 days after receipt of the
request. The request must include
sufficient information to support the
removal of the clinical hold.
In the Federal Register of May 14,
1998 (63 FR 26809), FDA published a
notice of availability of a guidance that
described how applicants should submit
responses to clinical holds so that they
may be identified as complete responses
and the agency can track the time to
respond.
FDA issued a revised guidance in
October 2000 which states that FDA will
respond in writing within 30 calendar
days of receipt of a sponsor’s request to
release a clinical hold and a complete
response to the issue(s) that led to the
clinical hold. An applicant’s complete
response to an IND clinical hold is a
response in which all clinical hold
issues identified in the clinical hold
letter have been addressed.
The guidance requests that applicants
type ‘‘Clinical Hold Complete
Response’’ in large, bold letters at the
top of the cover letter of the complete
response to expedite review of the
response. The guidance also requests
that applicants submit the complete
response letter in triplicate to the IND,
and that they fax a copy of the cover
letter to FDA’s contact listed in the
clinical hold letter who is responsible
for the IND. The guidance requests more
than an original and two copies of the
cover letter in order to ensure that the
30143
submission is received and handled in
a timely manner.
Based on data concerning the number
of complete responses to clinical holds
received by the Center for Drug
Evaluation and Research (CDER) in 2004
and 2005, CDER estimates that
approximately 88 responses are
submitted annually from approximately
67 applicants, and that it takes
approximately 284 hours to prepare and
submit to CDER each response.
Based on data concerning the number
of complete responses to clinical holds
received by the Center for Biologics
Evaluation and Research (CBER) in 2004
and 2005, CBER estimates that
approximately 92 responses are
submitted annually from approximately
60 applicants, and that it takes
approximately 284 hours to prepare and
submit to CBER each response.
TABLE 1—ESTIMATED ANNUAL REPORTING BURDEN1
Complete Responses to
Clinical Holds
No. of Responses Per
Respondent
No. of Respondents
Total Annual Responses
Hours Per Response
Total Hours
CDER
67
.76
88
284
24,992
CBER
60
1.53
92
284
26,128
Total
51,120
1There
are no capital costs or operating and maintenance costs associated with this collection of information.
Dated: May 18, 2006.
Jeffrey Shuren,
Assistant Commissioner for Policy.
[FR Doc. E6–7983 Filed 5–24–06; 8:45 am]
the Paperwork Reduction Act of 1995
(the PRA).
Fax written comments on the
collection of information by June 26,
2006.
DATES:
BILLING CODE 4160–01–S
Food and Drug Administration
[Docket No. 2006N–0080]
Agency Information Collection
Activities; Submission for Office of
Management and Budget Review;
Comment Request; Aluminum in Large
and Small Volume Parenterals Used in
Total Parenteral Nutrition
AGENCY:
Food and Drug Administration,
HHS.
ACTION:
Notice.
OMB is still experiencing
significant delays in the regular mail,
including first class and express mail,
and messenger deliveries are not being
accepted. To ensure that comments on
the information collection are received,
OMB recommends that written
comments be faxed to the Office of
Information and Regulatory Affairs,
OMB, Attn: Fumie Yokota, Desk Officer
for FDA, FAX: 202–395–6974.
ADDRESSES:
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
FOR FURTHER INFORMATION CONTACT:
Karen L. Nelson, Office of Management
Programs (HFA–250), Food and Drug
Administration, 5600 Fishers Lane,
Rockville, MD 20857, 301–827–1482.
In
compliance with 44 U.S.C. 3507, FDA
has submitted the following proposed
collection of information to OMB for
review and clearance.
cchase on PROD1PC60 with NOTICES
SUPPLEMENTARY INFORMATION:
The Food and Drug
Administration (FDA) is announcing
that a proposed collection of
information has been submitted to the
Office of Management and Budget
(OMB) for review and clearance under
SUMMARY:
VerDate Aug<31>2005
16:42 May 24, 2006
Jkt 208001
PO 00000
Frm 00031
Fmt 4703
Sfmt 4703
Aluminum in Large and Small Volume
Parenterals Used in Total Parenteral
Nutrition—21 CFR 201.323—(OMB
Control Number 0910–0439)—Extension
FDA is requesting OMB approval
under the PRA (44 U.S.C. 3501–3520),
for the labeling requirements for
aluminum content in large volume
parenterals (LVPs), small volume
parenterals (SVPs), and pharmacy bulk
packages (PBPs) used in total parenteral
nutrition (TPN). As explained in the
final rule on aluminum content labeling
requirements published in the Federal
Register of January 26, 2000 (65 FR
4103) (the January 2000 final rule),
aluminum content in parenteral drug
products could result in a toxic
accumulation of aluminum in the
tissues of individuals receiving TPN
therapy. Research indicates that
neonates and patient populations with
impaired kidney function may be at
high risk of exposure to unsafe amounts
of aluminum. Studies show that
aluminum may accumulate in the bone,
urine, and plasma of infants receiving
TPN. Many drug products used
routinely in parenteral therapy may
contain levels of aluminum sufficiently
E:\FR\FM\25MYN1.SGM
25MYN1
30144
Federal Register / Vol. 71, No. 101 / Thursday, May 25, 2006 / Notices
high to cause clinical manifestations.
Generally, when medication and
nutrition are administered orally, the
gastrointestinal tract acts as an efficient
barrier to the absorption of aluminum,
and relatively little ingested aluminum
actually reaches body tissues. However,
parenterally administered drug products
containing aluminum bypass the
protective mechanism of the
gastrointestinal tract and aluminum
circulates and is deposited in human
tissues.
Aluminum toxicity is difficult to
identify in infants because few reliable
techniques are available to evaluate
bone metabolism in premature infants.
Techniques used to evaluate the effects
of aluminum on bone in adults cannot
be used in premature infants. Although
aluminum toxicity is not commonly
detected clinically, it can be serious in
selected patient populations, such as
neonates, and may be more common
than is recognized.
FDA amended its regulations to add
labeling requirements for aluminum
content in LVPs, SVPs, and PBPs used
in TPN. FDA specified an upper limit of
aluminum permitted in LVPs and
required applicants to submit to FDA
validated assay methods for determining
aluminum content in parenteral drug
products. The agency added these
requirements because of evidence
linking the use of parenteral drug
products containing aluminum to
morbidity and mortality among patients
on TPN therapy, especially among
premature neonates and patients with
impaired kidney function.
The information collection reporting
requirements are as follows:
Section 201.323(b) (21 CFR
201.323(b)) requires that the package
insert of all LVPs used in TPN therapy
state that the drug product contains no
more than 25 micrograms (µg)/liter (L).
This information must be contained in
the ‘‘Precautions’’ section of the labeling
of all LVPs used in TPN therapy.
Section 201.323(c) (21 CFR
201.323(c)) requires that the maximum
level of aluminum present at expiry be
stated on the immediate container label
of all SVP drug products and PBPs used
in the preparation of TPN solutions. The
aluminum content must be stated as
prescribed in the regulation. The
immediate container label of all SVP
drug products and PBPs that are
lyophilized powders used in the
preparation of TPN solutions must
contain the statement prescribed in the
regulation.
Section 201.323(d) (21 CFR
201.323(d)) requires that the package
insert for all LVPs, SVPs, and PBPs used
in TPN contain a warning statement,
prescribed in the regulation, intended
for patients with impaired kidney
function and for neonates receiving TPN
therapy. This information must be
contained in the ‘‘Warnings’’ section of
the labeling.
Section 201.323(e) (21 CFR
201.323(e)) requires that applicants and
manufacturers must use validated assay
methods to determine the aluminum
content in parenteral drug products. The
assay methods must comply with
current good manufacturing practice
requirements. Applicants must submit
to FDA both validation of the method
used and release data for several
batches. Manufacturers of parenteral
drug products not subject to an
approved application must make assay
methodology available to FDA during
inspections. Holders of pending
applications must submit an
amendment to the application.
Compliance with the information
collection burdens under § 201.323(b),
(c), and (d) consists of submitting
application supplements to FDA
containing the revised labeling for each
product, and analytical method
validation must be submitted under
§ 201.323(e). During the period since the
publication of the January 2000 final
rule, FDA has received approximately
100 supplements and analytical method
validation from approximately four
respondents. Because the final rule was
effective on July 26, 2004, FDA expects
to receive fewer submissions per year.
FDA estimates that it will take
approximately 14 hours to prepare and
submit to FDA each submission.
In the Federal Register of February
27, 2006 (71 FR 9829), FDA published
a 60-day notice requesting public
comment on the information collection
provisions. No comments were received.
FDA estimates the burden of this
collection of information as follows:
TABLE 1.—ESTIMATED ANNUAL REPORTING BURDEN1
21 CFR Section
No. of
Respondents
Annual Frequency
per Response
Total Annual
Responses
Hours per
Response
Total Hours
201.323(b), (c), and (d)
4
1.25
5
14
70
201.323(e)
4
1.25
5
14
70
Total
1There
140
are no capital costs or operating and maintenance costs associated with this collection of information.
Dated: May 18, 2006.
Jeffrey Shuren,
Assistant Commissioner for Policy.
[FR Doc. E6–7984 Filed 5–24–06; 8:45 am]
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Food and Drug Administration
BILLING CODE 4160–01–S
cchase on PROD1PC60 with NOTICES
[Docket No. 2006N–0203]
Agency Information Collection
Activities; Proposed Collection;
Comment Request; User Fee Cover
Sheet; Form FDA 3397
AGENCY:
Food and Drug Administration,
HHS.
ACTION:
VerDate Aug<31>2005
16:42 May 24, 2006
Jkt 208001
PO 00000
Notice.
Frm 00032
Fmt 4703
Sfmt 4703
SUMMARY: The Food and Drug
Administration (FDA) is announcing an
opportunity for public comment on the
proposed collection of certain
information by the agency. Under the
Paperwork Reduction Act of 1995 (the
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
User Fee Cover Sheet; Form FDA 3397
that must be submitted along with
E:\FR\FM\25MYN1.SGM
25MYN1
Agencies
[Federal Register Volume 71, Number 101 (Thursday, May 25, 2006)]
[Notices]
[Pages 30143-30144]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: E6-7984]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Food and Drug Administration
[Docket No. 2006N-0080]
Agency Information Collection Activities; Submission for Office
of Management and Budget Review; Comment Request; Aluminum in Large and
Small Volume Parenterals Used in Total Parenteral Nutrition
AGENCY: Food and Drug Administration, HHS.
ACTION: Notice.
-----------------------------------------------------------------------
SUMMARY: The Food and Drug Administration (FDA) is announcing that a
proposed collection of information has been submitted to the Office of
Management and Budget (OMB) for review and clearance under the
Paperwork Reduction Act of 1995 (the PRA).
DATES: Fax written comments on the collection of information by June
26, 2006.
ADDRESSES: OMB is still experiencing significant delays in the regular
mail, including first class and express mail, and messenger deliveries
are not being accepted. To ensure that comments on the information
collection are received, OMB recommends that written comments be faxed
to the Office of Information and Regulatory Affairs, OMB, Attn: Fumie
Yokota, Desk Officer for FDA, FAX: 202-395-6974.
FOR FURTHER INFORMATION CONTACT: Karen L. Nelson, Office of Management
Programs (HFA-250), Food and Drug Administration, 5600 Fishers Lane,
Rockville, MD 20857, 301-827-1482.
SUPPLEMENTARY INFORMATION: In compliance with 44 U.S.C. 3507, FDA has
submitted the following proposed collection of information to OMB for
review and clearance.
Aluminum in Large and Small Volume Parenterals Used in Total Parenteral
Nutrition--21 CFR 201.323--(OMB Control Number 0910-0439)--Extension
FDA is requesting OMB approval under the PRA (44 U.S.C. 3501-3520),
for the labeling requirements for aluminum content in large volume
parenterals (LVPs), small volume parenterals (SVPs), and pharmacy bulk
packages (PBPs) used in total parenteral nutrition (TPN). As explained
in the final rule on aluminum content labeling requirements published
in the Federal Register of January 26, 2000 (65 FR 4103) (the January
2000 final rule), aluminum content in parenteral drug products could
result in a toxic accumulation of aluminum in the tissues of
individuals receiving TPN therapy. Research indicates that neonates and
patient populations with impaired kidney function may be at high risk
of exposure to unsafe amounts of aluminum. Studies show that aluminum
may accumulate in the bone, urine, and plasma of infants receiving TPN.
Many drug products used routinely in parenteral therapy may contain
levels of aluminum sufficiently
[[Page 30144]]
high to cause clinical manifestations. Generally, when medication and
nutrition are administered orally, the gastrointestinal tract acts as
an efficient barrier to the absorption of aluminum, and relatively
little ingested aluminum actually reaches body tissues. However,
parenterally administered drug products containing aluminum bypass the
protective mechanism of the gastrointestinal tract and aluminum
circulates and is deposited in human tissues.
Aluminum toxicity is difficult to identify in infants because few
reliable techniques are available to evaluate bone metabolism in
premature infants. Techniques used to evaluate the effects of aluminum
on bone in adults cannot be used in premature infants. Although
aluminum toxicity is not commonly detected clinically, it can be
serious in selected patient populations, such as neonates, and may be
more common than is recognized.
FDA amended its regulations to add labeling requirements for
aluminum content in LVPs, SVPs, and PBPs used in TPN. FDA specified an
upper limit of aluminum permitted in LVPs and required applicants to
submit to FDA validated assay methods for determining aluminum content
in parenteral drug products. The agency added these requirements
because of evidence linking the use of parenteral drug products
containing aluminum to morbidity and mortality among patients on TPN
therapy, especially among premature neonates and patients with impaired
kidney function.
The information collection reporting requirements are as follows:
Section 201.323(b) (21 CFR 201.323(b)) requires that the package
insert of all LVPs used in TPN therapy state that the drug product
contains no more than 25 micrograms (microg)/liter (L). This
information must be contained in the ``Precautions'' section of the
labeling of all LVPs used in TPN therapy.
Section 201.323(c) (21 CFR 201.323(c)) requires that the maximum
level of aluminum present at expiry be stated on the immediate
container label of all SVP drug products and PBPs used in the
preparation of TPN solutions. The aluminum content must be stated as
prescribed in the regulation. The immediate container label of all SVP
drug products and PBPs that are lyophilized powders used in the
preparation of TPN solutions must contain the statement prescribed in
the regulation.
Section 201.323(d) (21 CFR 201.323(d)) requires that the package
insert for all LVPs, SVPs, and PBPs used in TPN contain a warning
statement, prescribed in the regulation, intended for patients with
impaired kidney function and for neonates receiving TPN therapy. This
information must be contained in the ``Warnings'' section of the
labeling.
Section 201.323(e) (21 CFR 201.323(e)) requires that applicants and
manufacturers must use validated assay methods to determine the
aluminum content in parenteral drug products. The assay methods must
comply with current good manufacturing practice requirements.
Applicants must submit to FDA both validation of the method used and
release data for several batches. Manufacturers of parenteral drug
products not subject to an approved application must make assay
methodology available to FDA during inspections. Holders of pending
applications must submit an amendment to the application.
Compliance with the information collection burdens under Sec.
201.323(b), (c), and (d) consists of submitting application supplements
to FDA containing the revised labeling for each product, and analytical
method validation must be submitted under Sec. 201.323(e). During the
period since the publication of the January 2000 final rule, FDA has
received approximately 100 supplements and analytical method validation
from approximately four respondents. Because the final rule was
effective on July 26, 2004, FDA expects to receive fewer submissions
per year. FDA estimates that it will take approximately 14 hours to
prepare and submit to FDA each submission.
In the Federal Register of February 27, 2006 (71 FR 9829), FDA
published a 60-day notice requesting public comment on the information
collection provisions. No comments were received.
FDA estimates the burden of this collection of information as
follows:
Table 1.--Estimated Annual Reporting Burden\1\
--------------------------------------------------------------------------------------------------------------------------------------------------------
No. of Annual Frequency Total Annual Hours per
21 CFR Section Respondents per Response Responses Response Total Hours
--------------------------------------------------------------------------------------------------------------------------------------------------------
201.323(b), (c), and (d) 4 1.25 5 14 70
--------------------------------------------------------------------------------------------------------------------------------------------------------
201.323(e) 4 1.25 5 14 70
--------------------------------------------------------------------------------------------------------------------------------------------------------
Total 140
--------------------------------------------------------------------------------------------------------------------------------------------------------
\1\There are no capital costs or operating and maintenance costs associated with this collection of information.
Dated: May 18, 2006.
Jeffrey Shuren,
Assistant Commissioner for Policy.
[FR Doc. E6-7984 Filed 5-24-06; 8:45 am]
BILLING CODE 4160-01-S