Agency Information Collection Activities; Submission for Office of Management and Budget Review; Comment Request; Application for Food and Drug Administration Approval To Market a New Drug
Federal Register, Volume 79 Issue 180 (Wednesday, September 17, 2014)
Federal Register Volume 79, Number 180 (Wednesday, September 17, 2014)
Notices
Pages 55801-55804
From the Federal Register Online via the Government Printing Office www.gpo.gov
FR Doc No: 2014-22088
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DEPARTMENT OF HEALTH AND HUMAN SERVICES
Food and Drug Administration
Docket No. FDA-2010-N-0627
Agency Information Collection Activities; Submission for Office of Management and Budget Review; Comment Request; Application for Food and Drug Administration Approval To Market a New Drug
AGENCY: Food and Drug Administration, HHS.
ACTION: Notice.
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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.
DATES: Fax written comments on the collection of information by October 17, 2014.
ADDRESSES: 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: FDA Desk Officer, FAX: 202-395-7285, or emailed to oirasubmission@omb.eop.gov. All comments should be identified with the OMB control number 0910-
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Also include the FDA docket number found in brackets in the heading of this document.
FOR FURTHER INFORMATION CONTACT: FDA PRA Staff, Office of Operations, Food and Drug Administration, 8455 Colesville Rd., COLE-14526, Silver Spring, MD 20993-0002, PRAStaff@fda.hhs.gov.
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.
Application for FDA Approval to Market a New Drug--(OMB Control Number 0910-0001)--Extension
Under section 505(a) of the Federal Food, Drug, and Cosmetic Act (the FD&C Act) (21 U.S.C. 355(a)), a new drug may not be commercially marketed in the United States, imported, or exported from the United States, unless an approval of an application filed with FDA under section 505(b) or 505(j) of the act is effective with respect to such drug. Under the FD&C Act, it is the sponsor's responsibility to provide the information needed by FDA to make a scientific and technical determination whether the product is safe and effective for use.
This approval request is for all information collection requirements imposed on applicants by the regulations under part 314 (21 CFR part 314) who apply for approval of a new drug application (NDA) or abbreviated new drug application (ANDA) in order to market or to continue to market a drug.
Section 314.50(a) requires that an application form (Form FDA 356h) be submitted that includes introductory information about the drug as well as a checklist of enclosures.
Section 314.50(b) requires that an index be submitted with the archival copy of the application and that it reference certain sections of the application.
Section 314.50(c) requires that a summary of the application be submitted that presents a good general synopsis of all the technical sections and other information in the application.
Section 314.50(d) requires that the NDA contain the following technical sections about the new drug: Chemistry, manufacturing, and controls; nonclinical pharmacology and toxicology; human pharmacokinetics and bioavailability; microbiology; clinical data; statistical; and pediatric use sections.
Section 314.50(e) requires the applicant to submit samples of the drug if requested by FDA. In addition, the archival copy of the application must include copies of the label and all labeling for the drug.
Section 314.50(f) requires that case report forms and tabulations be submitted with the archival copy.
Section 314.50(h) requires that patent information, as described under Sec. 314.53, be submitted with the application. (The burden hours for Sec. 314.50(h) are already approved by OMB under OMB control number 0910-0513 and are not included in the burden estimates in Table 1 of this document.)
Section 314.50(i) requires that patent certification information be submitted in section 505(b)(2) applications for patents claiming the drug, drug product, or method of use.
Section 314.50(j) requires that applicants that request a period of marketing exclusivity submit certain information with the application.
Section 314.50(k) requires that the application contain a financial certification or disclosure statement or both.
Section 314.50(l) requires that an archival, review, and field copy of the application be submitted, including the content of labeling and all labeling and labels.
Section 314.52 requires that any notice of certification of invalidity or non-infringement of a patent to each patent owner and the NDA holder be sent by a section 505(b)(2) applicant that relies on a listed drug. A 505(b)(2) applicant is required to amend its application at the time notice is provided to include a statement certifying that the required notice has been provided. A 505(b)(2) applicant also is required to amend its application to document receipt of the required notice.
Section 314.54 sets forth the content requirements for applications filed under section 505(b)(2) of the FD&C Act. (The information collection burden estimate for 505(b)(2) applications is included in table 1 of this document under the estimates for Sec. 314.50 (a), (b), (c), (d), (e), (f), (g), (i), (j), (k) and (l)).
Section 314.60 sets forth reporting requirements for sponsors who amend an unapproved application.
Section 314.65 states that the sponsor must notify FDA when withdrawing an unapproved application.
Sections 314.70 and 314.71 require that supplements be submitted to FDA for certain changes to an approved application.
Section 314.72 requires sponsors to report to FDA any transfer of ownership of an application.
Section 314.80(c)(1) and (c)(2) sets forth requirements for expedited adverse drug experience postmarketing reports and followup reports, as well as for periodic adverse drug experience postmarketing reports (Form FDA 3500A). (The burden hours for Sec. 314.80(c)(1) and (c)(2) are already approved by OMB under OMB control numbers 0910-0230 and 0910-0291 and are not included in the burden estimates in table 1 of this document.)
Section 314.80(i) establishes recordkeeping requirements for reports of postmarketing adverse drug experiences. (The burden hours for
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Sec. 314.80(i) are already approved by OMB under OMB control numbers 0910-0230 and 0910-0291 and are not included in the burden estimates in table 1 of this document.)
Section 314.81(b)(1) requires that field alert reports be submitted to FDA (Form FDA 3331).
Section 314.81(b)(2) requires that annual reports be submitted to FDA (Form FDA 2252).
Section 314.81(b)(3)(i) requires that drug advertisements and promotional labeling be submitted to FDA (Form FDA 2253).
Section 314.81(b)(3)(iii) sets forth reporting requirements for sponsors who withdraw an approved drug product from sale. (The burden hours for Sec. 314.81(b)(3)(iii) are already approved by OMB under OMB control number 0910-0045 and are not included in the burden estimates in table 1 of this document.)
Section 314.90 sets forth requirements for sponsors who request waivers from FDA for compliance with Sec. Sec. 314.50 through 314.81. (The information collection burden estimate for NDA waiver requests is included in table 1 of this document under the estimates for each section that is in subpart B of part 314.)
Section 314.93 sets forth requirements for submitting a suitability petition in accordance with Sec. 10.20 (21 CFR 10.20) and Sec. 10.30. (The burden hours for Sec. 314.93 are already approved by OMB under 0910-0183 and are not included in the burden estimates in table 1 of this document.)
Section 314.94(a) and (d) requires that an ANDA contain the following information: Application form; table of contents; basis for ANDA submission; conditions of use; active ingredients; route of administration, dosage form, and strength; bioequivalence; labeling; chemistry, manufacturing, and controls; samples; patent certification.
Section 314.95 requires that any notice of certification of invalidity or non-infringement of a patent to each patent owner and the NDA holder be sent by ANDA applicants.
Section 314.96 sets forth requirements for amendments to an unapproved ANDA.
Section 314.97 sets forth requirements for submitting supplements to an approved ANDA for certain changes to the application.
Section 314.98(a) sets forth postmarketing adverse drug experience reporting and recordkeeping requirements for ANDAs. (The burden hours for Sec. 314.98(a) are already approved by OMB under OMB control numbers 0910-0230 and 0910-0291 and are not included in the burden estimates in table 1 of this document.)
Section 314.98(c) requires other postmarketing reports for ANDAs: Field alert reports (Form FDA 3331), annual reports (Form FDA 2252), and advertisements and promotional labeling (Form FDA 2253). (The information collection burden estimate for field alert reports is included in table 1 of this document under Sec. 314.81(b)(1); the estimate for annual reports is included under Sec. 314.81(b)(2); the estimate for advertisements and promotional labeling is included under Sec. 314.81(b)(3)(i).)
Section 314.99(a) requires that sponsors comply with certain reporting requirements for withdrawing an unapproved ANDA and for a change in ownership of an ANDA.
Section 314.99(b) sets forth requirements for sponsors who request waivers from FDA for compliance with Sec. Sec. 314.92 through 314.99. (The information collection burden estimate for ANDA waiver requests is included in table 1 of this document under the estimates for each section that is in subpart C of part 314.)
Section 314.101(a) states that if FDA refuses to file an application, the applicant may request an informal conference with FDA and request that the application be filed over protest.
Section 314.107(c) requires notice to FDA by the first applicant to submit a substantially complete ANDA containing a certification that a relevant patent is invalid, unenforceable, or will not be infringed of the date of first commercial marketing. (The information collection burden estimate for Sec. 314.107(c) is included in table 1 of this document under the estimates for Sec. 314.50 (a), (b), (c), (d), (e), (f), (g), (i), (j), (k) and (l)).
Section 314.107(e) requires that an applicant submit a copy of the entry of the order or judgment to FDA within 10 working days of a final judgment. (The information collection burden estimate for Sec. 314.107(e) applications is included in table 1 of this document under the estimates for Sec. 314.50 (a), (b), (c), (d), (e), (f), (g), (i), (j), (k) and (l)).
Section 314.107(f) requires that ANDA or section 505(b)(2) applicants notify FDA immediately of the filing of any legal action filed within 45 days of receipt of the notice of certification. A patent owner may also notify FDA of the filing of any legal action for patent infringement. If the patent owner or approved application holder who is an exclusive patent licensee waives its opportunity to file a legal action for patent infringement within the 45-day period, the patent owner or approved application holder must submit to FDA a waiver in the specified format. (The information collection burden estimate for Sec. 314.107(f) is included in table 1 of this document under the estimates for Sec. 314.50 (a), (b), (c), (d), (e), (f), (g), (i), (j), (k) and (l)).
Section 314.110(b)(3) states that, after receipt of an FDA complete response letter, an applicant may request an opportunity for a hearing on the question of whether there are grounds for denying approval of the application. (The burden hours for Sec. 314.110(b)(3) are included under parts 10 through 16 (21 CFR parts 10 and 16) hearing regulations, in accordance with Sec. 314.201, and are not included in the burden estimates in table 1 of this document.)
Section 314.122(a) requires that an ANDA or a suitability petition that relies on a listed drug that has been voluntarily withdrawn from sale must be accompanied by a petition seeking a determination whether the drug was withdrawn for safety or effectiveness reasons. (The burden hours for Sec. 314.122(a) are already approved by OMB under OMB control number 0910-0183 and are not included in the burden estimates in table 1 of this document.)
Section 314.122(d) sets forth requirements for relisting petitions for unlisted discontinued products. (The burden hours for Sec. 314.122(d) are already approved by OMB under OMB control number 0910-
0183 and are not included in the burden estimates in table 1 of this document.)
Section 314.126(c) sets forth requirements for a petition to waive criteria for adequate and well-controlled studies. (The burden hours for Sec. 314.126(c) are already approved by OMB under 0910-0183 and are not included in the burden estimates in table 1 of this document.)
Section 314.151(a) and (b) set forth requirements for the withdrawal of approval of an ANDA and the applicant's opportunity for a hearing and submission of comments. (The burden hours for Sec. 314.151(a) and (b) are included under parts 10 through 16 hearing regulations, in accordance with Sec. 314.201, and are not included in the burden estimates in table 1 of this document.)
Section 314.151(c) sets forth the requirements for withdrawal of approval of an ANDA and the applicant's opportunity to submit written objections and participate in a limited oral hearing. (The burden hours for Sec. 314.151(c) are included under parts 10 through 16 hearing regulations, in accordance with Sec. 314.201, and are not included in the
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burden estimates in table 1 of this document.)
Section 314.153(b) sets forth the requirements for suspension of an ANDA when the listed drug is voluntarily withdrawn for safety and effectiveness reasons, and the applicant's opportunity to present comments and participate in a limited oral hearing. (The burden hours for Sec. 314.152(b) are included under parts 10 through 16 hearing regulations, in accordance with Sec. 314.201, and are not included in the burden estimates in table 1 of this document.)
Section 314.161(b) and (e) sets forth the requirements for submitting a petition to determine whether a listed drug was voluntarily withdrawn from sale for safety or effectiveness reasons. (The burden hours for Sec. 314.161(b) and (e) are already approved by OMB under OMB control number 0910-0183 and are not included in the burden estimates in table 1 of this document.)
Section 314.200(c), (d), and (e) requires that applicants or others subject to a notice of opportunity for a hearing who wish to participate in a hearing file a written notice of participation and request for a hearing as well as the studies, data, and so forth, relied on. Other interested persons may also submit comments on the notice. This section also sets forth the content and format requirements for the applicants' submission in response to notice of opportunity for hearing. (The burden hours for Sec. 314.200(c), (d), and (e) are included under parts 10 through 16 hearing regulations, in accordance with Sec. 314.201, and are not included in the burden estimates in table 1 of this document.)
Section 314.200(f) states that participants in a hearing may make a motion to the presiding officer for the inclusion of certain issues in the hearing. (The burden hours for Sec. 314.200(f) are included under parts 10 through 16 hearing regulations, in accordance with Sec. 314.201, and are not included in the burden estimates in table 1 of this document.)
Section 314.200(g) states that a person who responds to a proposed order from FDA denying a request for a hearing provide sufficient data, information, and analysis to demonstrate that there is a genuine and substantial issue of fact which justifies a hearing. (The burden hours for Sec. 314.200(g) are included under parts 10 through 16 hearing regulations, in accordance with Sec. 314.201, and are not included in the burden estimates in table 1 of this document.)
Section 314.420 states that an applicant may submit to FDA a drug master file in support of an application, in accordance with certain content and format requirements.
Section 314.430 states that data and information in an application are disclosable under certain conditions, unless the applicant shows that extraordinary circumstances exist. (The burden hours for Sec. 314.430 are included under parts 10 through 16 hearing regulations, in accordance with Sec. 314.201, and are not included in the burden estimates in table 1 of this document.)
Section 314.530(c) and (e) states that if FDA withdraws approval of a drug approved under the accelerated approval procedures, the applicant has the opportunity to request a hearing and submit data and information. (The burden hours for Sec. 314.530(c) and (e) are included under parts 10 through 16 hearing regulations, in accordance with Sec. 314.201, and are not included in the burden estimates in table 1 of this document.)
Section 314.530(f) requires that an applicant first submit a petition for stay of action before requesting an order from a court for a stay of action pending review. (The burden hours for Sec. 314.530(f) are already approved by OMB under 0910-0194 and are not included in the burden estimates in table 1 of this document.)
Section 314.550 requires an applicant with a new drug product being considered for accelerated approval to submit copies of all promotional materials to FDA during the preapproval and post-approval periods.
Section 314.610(b)(1) requires that applicants include a plan or approach to postmarketing study commitments in applications for approval of new drugs when human efficacy studies are not ethical or feasible, and provide status reports of postmarketing study commitments. (The information collection burden estimate for Sec. 314.610(b)(1) is included in table 1 of this document under the estimates for Sec. Sec. 314.50 (a), (b), (c), (d), (e), (f), (k) and (l) and 314.81(b)(2)).
Section 314.610(b)(3) requires that applicants propose labeling to be provided to patient recipients in applications for approval of new drugs when human efficacy studies are not ethical or feasible. (The information collection burden estimate for Sec. 314.610(b)(3) is included in table 1 of this document under the estimates for Sec. 314.50(e)).
Section 314.630 requires that applicants provide postmarketing safety reporting for applications for approval of new drugs when human efficacy studies are not ethical or feasible. (The burden hours for Sec. 314.630 are already approved by OMB under OMB control numbers 0910-0230 and 0910-0291 and are not included in the burden estimates in table 1 of this document.)
Section 314.640 requires that applicants provide promotional materials for applications for approval of new drugs when human efficacy studies are not ethical or feasible. (The information collection burden estimate for Sec. 314.640 is included in table 1 of this document under the estimates for Sec. 314.81(b)(3)(i)).
Respondents to this collection of information are all persons who submit an application or abbreviated application or an amendment or supplement to FDA under Part 314 to obtain approval of a new drug, and any person who owns an approved application or abbreviated application.
In the Federal Register of March 24, 2014 (79 FR 16003), FDA published a 60-day notice requesting public comment on the proposed collection of information. We received one comment. The comment requested clarification of the duties, responsibilities, and potential liabilities of the person denoted as the ``Authorized U.S. Agent'' in field 39 of Form FDA 356h. The comment also requested that the formatting for field 39 be revised to clarify, ``What exactly it is that the Authorized U.S. Agent is attesting to by its signature.''
FDA response: Neither the form nor the instructions are intended to capture the exact duties, responsibilities, and potential liabilities of the person identified in field 39. Rather, as the instructions indicate, field 39 is intended to capture a countersignature where one is required in accordance with 21 CFR 314.50(a)(5): If the person signing the form in Field 38 does not reside or have a place of business within the United States, the form must be countersigned in Field 39 by an attorney, agent, or other authorized official who resides or maintains a place of business within the United States.
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Table 1--Estimated Annual Reporting Burden
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Number of Average
21 CFR Section; FDA Form No. Number of responses per Total annual burden per Total hours
respondents respondent responses response
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314.50(a), (b), (c), (d), (e), 106 1.42 151 1,921 290,071
(f), (g), (i), (j), (k) and (l)
356h.........................
314.52.......................... 7 3 21 16 336
314.95.......................... 209 3 627 16 10,032
314.60.......................... 277 8.73 2,419 80 193,520
314.65.......................... 18 1.16 21 2 42
314.70 and 314.71............... 374 7.63 2,854 150 428,100
314.72.......................... 66 2.20 145 2 290
314.81(b)(1) 3331............. 260 16.31 4,241 8 33,928
314.81(b)(2) 2252............. 930 11.28 10,495 40 419,800
314.81(b)(3)(i) 2253.......... 520 87.43 45,461 2 90,922
314.94(a) and (d)............... 251 4.73 1,186 480 569,280
314.96.......................... 434 24.60 10,675 80 854,000
314.97.......................... 306 18.34 5,611 80 448,880
314.99(a)....................... 219 3.01 659 2 1,318
314.101(a)...................... 1 1 1 * .50 .50
314.420......................... 524 1.98 1,038 61 63,318
314.550......................... 20 7 140 120 16,800
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Total....................... .............. .............. .............. .............. 3,420,637.50
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There are no capital costs or operating and maintenance costs associated with this collection of information.
* 30 minutes.
Dated: September 11, 2014.
Leslie Kux,
Assistant Commissioner for Policy.
FR Doc. 2014-22088 Filed 9-16-14; 8:45 am
BILLING CODE 4164-01-P
