Formal-Meetings-Between-the-FDA-and-Sponsors-or-Applicants-of-BsUFA-Products-Guidance-for-Industry

Formal Meetings Between
the FDA and Sponsors or
Applicants of BsUFA
Products
Guidance for Industry
DRAFT GUIDANCE
This guidance document is being distributed for comment purposes only.
Comments and suggestions regarding this draft document should be submitted within 90 days of
publication in the Federal Register of the notice announcing the availability of the draft
guidance. Submit electronic comments to https://www.regulations.gov. Submit written
comments to the Dockets Management Staff (HFA-305), Food and Drug Administration, 5630
Fishers Lane, Rm. 1061, Rockville, MD 20852. All comments should be identified with the
docket number listed in the notice of availability that publishes in the Federal Register.
For questions regarding this draft document, contact (CDER) Neel Patel at 301-796-0970 or
(CBER) the Office of Communication, Outreach, and Development at 800-835-4709 or 240-4028010.

U.S. Department of Health and Human Services
Food and Drug Administration
Center for Drug Evaluation and Research (CDER)
Center for Biologics Evaluation and Research (CBER)
June 2018
Procedural

18958449dft.docx
5/31/2018

Formal Meetings Between
the FDA and Sponsors or
Applicants of BsUFA
Products
Guidance for Industry
Additional copies are available from:
Office of Communications, Division of Drug Information
Center for Drug Evaluation and Research
Food and Drug Administration
10001 New Hampshire Ave., Hillandale Bldg., 4th Floor
Silver Spring, MD 20993-0002
Phone: 855-543-3784 or 301-796-3400; Fax: 301-431-6353; Email: druginfo@fda.hhs.gov
https://www.fda.gov/Drugs/GuidanceComplianceRegulatoryInformation/Guidances/default.htm
and/or
Office of Communication, Outreach, and Development
Center for Biologics Evaluation and Research
Food and Drug Administration
10903 New Hampshire Ave., Bldg. 71, rm. 3128
Silver Spring, MD 20993-0002
Phone: 800-835-4709 or 240-402-8010; Email: ocod@fda.hhs.gov
https://www.fda.gov/BiologicsBloodVaccines/GuidanceComplianceRegulatoryInformation/Guidances/default.htm

U.S. Department of Health and Human Services
Food and Drug Administration
Center for Drug Evaluation and Research (CDER)
Center for Biologics Evaluation and Research (CBER)
June 2018
Procedural

TABLE OF CONTENTS
I.

INTRODUCTION............................................................................................................. 1

II.

BACKGROUND ............................................................................................................... 2

III.

MEETING TYPES ........................................................................................................... 2

A.

BIA Meeting ................................................................................................................................... 3

B.

BPD Type 1 Meeting ...................................................................................................................... 3

C.

BPD Type 2 Meeting ...................................................................................................................... 4

D.

BPD Type 3 Meeting ...................................................................................................................... 4

E.

BPD Type 4 Meeting ...................................................................................................................... 5

IV.

BSUFA FEES ASSOCIATED WITH THE BPD PROGRAM..................................... 5

V.

MEETING FORMATS .................................................................................................... 5

VI.

MEETING REQUESTS ................................................................................................... 6

VII.

ASSESSING AND RESPONDING TO MEETING REQUESTS ................................ 8

A.

Meeting Denied .............................................................................................................................. 9

B.

Meeting Granted ............................................................................................................................ 9

VIII. MEETING PACKAGE .................................................................................................. 10
A.

Timing of Meeting Package Submission .................................................................................... 10

B.

Where and How Many Copies of Meeting Packages to Send .................................................. 10

C.

Meeting Package Content............................................................................................................ 11

IX.

PRELIMINARY RESPONSES ..................................................................................... 12

X.

RESCHEDULING MEETINGS.................................................................................... 13

XI.

CANCELING MEETINGS ........................................................................................... 14

XII.

MEETING CONDUCT .................................................................................................. 14

XIII. MEETING MINUTES.................................................................................................... 15
REFERENCES ............................................................................................................................ 17

Contains Nonbinding Recommendations
Draft — Not for Implementation

Formal Meetings Between the FDA and
Sponsors or Applicants of BsUFA Products
Guidance for Industry 1

1
2
3
4
5
6
7
8
9
10
11
12
13
14
15
16
17
18
19
20
21
22
23
24
25
26
27
28
29
30
31
32

This draft guidance, when finalized, will represent the current thinking of the Food and Drug
Administration (FDA or Agency) on this topic. It does not establish any rights for any person and is not
binding on FDA or the public. You can use an alternative approach if it satisfies the requirements of the
applicable statutes and regulations. To discuss an alternative approach, contact the FDA staff responsible
for this guidance as listed on the title page.

I.

INTRODUCTION

This guidance provides recommendations to industry on formal meetings between the Food and
Drug Administration (FDA) and sponsors or applicants relating to the development and review
of biosimilar or interchangeable biological products regulated by the Center for Drug Evaluation
and Research (CDER) or the Center for Biologics Evaluation and Research (CBER). This
guidance does not apply to meetings associated with the development of products intended for
submission in, or with the review of, new drug applications or abbreviated new drug applications
under section 505 of the Federal Food, Drug and Cosmetic Act (FD&C Act), biologics license
applications (BLAs) under section 351(a) of the Public Health Service Act (PHS Act), or
submissions for devices under the FD&C Act. 2 For the purposes of this guidance, formal
meeting includes any meeting that is requested by a sponsor or applicant (hereafter referred to as
requester(s)) following the procedures provided in this guidance and includes meetings
conducted in any format (i.e., face to face, teleconference/videoconference, or written response
only (WRO)).

1

This guidance has been prepared by the Center for Drug Evaluation and Research (CDER) in cooperation with the
Center for Biologics Evaluation and Research (CBER) at the Food and Drug Administration.

2

For information on meetings for new drug applications and 351(a) BLAs, see the draft guidance for industry
Formal Meetings Between the FDA and Sponsors or Applicants of PDUFA Products. When final, this guidance will
represent the FDA’s current thinking on this topic. For the most recent version of a guidance, check the FDA Drugs
or Biologics guidance web pages at
https://www.fda.gov/Drugs/GuidanceComplianceRegulatoryInformation/Guidances/default.htm and
https://www.fda.gov/BiologicsBloodVaccines/GuidanceComplianceRegulatoryInformation/Guidances/default.htm.

1

Contains Nonbinding Recommendations
Draft — Not for Implementation

33
34
35
36
37
38
39
40
41
42
43
44
45
46
47
48
49
50
51
52
53
54
55
56
57
58
59
60
61
62
63
64
65

This guidance discusses the principles of good meeting management practices (GMMPs) and
describes standardized procedures for requesting, preparing, scheduling, conducting, and
documenting such formal meetings. 3
In general, FDA’s guidance documents do not establish legally enforceable responsibilities.
Instead, guidances describe the Agency’s current thinking on a topic and should be viewed only
as recommendations, unless specific regulatory or statutory requirements are cited. The use of
the word should in Agency guidances means that something is suggested or recommended, but
not required.

II.

BACKGROUND

Each year, FDA review staff participate in many meetings with requesters who seek advice
relating to the development and review of a biosimilar or interchangeable product. Because
these meetings often represent critical points in the regulatory and development process, it is
important that there are efficient, consistent procedures for the timely and effective conduct of
such meetings. The GMMPs in this guidance are intended to provide consistent procedures that
will promote well-managed meetings and to ensure that such meetings are scheduled within a
reasonable time, conducted efficiently, and documented appropriately.
As part of the reauthorization of the Biosimilar User Fee Act (BsUFA), 4 the FDA has committed
to specific performance goals that include meeting management goals for formal meetings that
occur between the FDA and requesters. 5

III.

MEETING TYPES 6

There are five types of formal meetings that occur between requesters and FDA staff to discuss
development and review of a biosimilar or interchangeable product: Biosimilar Initial Advisory
(BIA), Biosimilar Biological Product Development (BPD) Type 1, BPD Type 2, BPD Type 3,
and BPD Type 4.

3

The previous guidance for industry Formal Meetings Between the FDA and Biosimilar Biological Product
Sponsors or Applicants published November 18, 2015, has been withdrawn.

4

The Biosimilar User Fee Act of 2012 (BsUFA I) added sections 744G and 744H to the FD&C Act, authorizing
FDA to collect user fees for a 5-year period from persons that develop biosimilar biological products. BsUFA was
reauthorized for a 5-year period in 2017 under Title IV of the FDA Reauthorization Act of 2017 (BsUFA II),
enacted on August 18, 2017.

5

See the BsUFA II goals letter titled “BsUFA Reauthorization Performance Goals and Procedures Fiscal Years
2018 Through 2022” available on the FDA website at
https://www.fda.gov/downloads/ForIndustry/UserFees/BiosimilarUserFeeActBsUFA/UCM521121.pdf.

6

The meeting types and goal dates are described in the BsUFA II goals letter and apply to formal meetings between
FDA staff and requesters of BsUFA meetings; they do not apply to meetings with CDER Office of Generic Drugs,
CDER Office of Compliance, or CDER Office of Prescription Drug Promotion.

2

Contains Nonbinding Recommendations
Draft — Not for Implementation

66
67
68
69
70
71
72
73
74
75
76
77
78
79
80
81
82
83
84
85
86
87
88
89
90
91
92
93
94
95
96
97
98
99
100
101
102
103
104
105
106
107
108

Requesters are not required to request meetings in sequential order (i.e., BIA, BPD Type 2, BPD
Type 3, then BPD Type 4). The meeting type requested depends on the stage of the development
program and/or the advice being sought. Although the FDA would, in general, grant one BIA
meeting and one BPD Type 4 meeting for a particular biosimilar or interchangeable product,
requesters can request, as appropriate, as many BPD Type 2 and Type 3 meetings as needed to
support the development and review of a biosimilar or interchangeable product.
A.

BIA Meeting

A BIA meeting is an initial assessment limited to a general discussion regarding whether
licensure under section 351(k) of the PHS Act may be feasible for a particular product, and if so,
general advice on the expected content of the development program. This meeting type does not
include any meeting that involves substantive review of summary data or full study reports.
However, preliminary comparative analytical similarity data from at least one lot of the proposed
biosimilar or interchangeable product compared to the U.S.-licensed reference product should be
provided in the meeting package. The analytical similarity data should be sufficient to enable the
FDA to make a preliminary determination as to whether licensure under section 351(k) of the
PHS Act may be feasible for a particular product and to provide meaningful advice. A general
overview of the development program, including synopses of results and findings from all
completed studies and information about planned studies, also should be provided.
Extensive analytical, nonclinical, and/or clinical data are not expected to be provided based on
the expected stage of development of the proposed biosimilar or interchangeable product. If the
requester is seeking targeted advice on the adequacy of any comparative data or extensive advice
for any aspect of a planned or ongoing biosimilar or interchangeable development program, a
different meeting type should be requested.
B.

BPD Type 1 Meeting

A BPD Type 1 meeting is a meeting that is necessary for an otherwise stalled development
program to proceed or a meeting to address an important safety issue. Examples of a BPD Type
1 meeting include the following:
•

Meetings to discuss clinical holds: (1) in which the requester seeks input on how to
address the hold issues; or (2) in which a response to hold issues has been submitted, and
reviewed by the FDA, but the FDA and the requester agree that the development is
stalled and a new path forward should be discussed.

•

Meetings that are requested after receipt of an FDA nonagreement Special Protocol
Assessment letter in response to protocols submitted under the special protocol
assessment procedures as described in the guidance for industry Special Protocol
Assessment. 7

7

We update guidances periodically. To make sure you have the most recent version of a guidance, check the FDA
guidance web page at https://www.fda.gov/RegulatoryInformation/Guidances/default.htm.

3

Contains Nonbinding Recommendations
Draft — Not for Implementation

109
110
111
112
113
114
115
116
117
118
119
120
121
122
123
124
125
126
127
128
129
130
131
132
133
134
135
136
137
138
139
140
141
142
143
144
145
146
147
148
149
150
151
152
153
154

•

Meetings to discuss an important safety issue, when such an issue is identified and the
FDA and requester agree that the issue should be discussed.

•

Dispute resolution meetings as described in 21 CFR 10.75 and 312.48 and in the
guidance for industry and review staff Formal Dispute Resolution: Sponsor Appeals
Above the Division Level.

•

Post-action meetings requested after an FDA regulatory action other than an approval
(i.e., issuance of a complete response letter).

•

Meetings requested within 30 days of FDA issuance of a refuse-to-file letter to discuss
whether the FDA should file the application.
C.

BPD Type 2 Meeting

A BPD Type 2 meeting is a meeting to discuss a specific issue (e.g., ranking of quality attributes;
chemistry, manufacturing, and controls such as control strategy; study design or endpoints; postapproval changes) or questions for which the FDA will provide targeted advice regarding an
ongoing development program. This meeting type may include substantive review of summary
data but does not include review of full study reports.
D.

BPD Type 3 Meeting

A BPD Type 3 meeting is an in-depth data review and advice meeting regarding an ongoing
development program. This meeting type includes substantive review of full study reports or an
extensive data package (e.g., detailed and robust analytical similarity data), FDA advice
regarding the similarity between the proposed biosimilar or interchangeable product and the
reference product based on a comprehensive data package, and FDA advice regarding the need
for additional studies, including design and analysis, based on a comprehensive data package.
•

•

Examples of a BPD Type 3 meeting submission include the following:
‒

Comprehensive analytical similarity data that permit the FDA to make a preliminary
evaluation of analytical similarity during development. The level of analytical data
provided should be similar to what the requester intends to submit in a 351(k) BLA
(e.g., full study reports and/or datasets that support the full study reports).

‒

Full study report(s) for a clinical study or clinical studies.

Based on the data and/or datasets and results reported in the full study reports, the FDA
encourages the requester to provide an update on the development plan of the proposed
biosimilar or interchangeable product. Examples of topics the requester can address as
part of a BPD Type 3 meeting in addition to the in-depth data submitted include the
following:
‒

Proposal for any planned additional studies

4

Contains Nonbinding Recommendations
Draft — Not for Implementation

155
156
157
158
159
160
161
162
163
164
165
166
167
168
169
170
171
172
173
174
175
176
177
178
179
180
181
182
183
184
185
186
187
188
189
190
191
192
193
194
195
196
197

‒
E.

Proposal for extrapolation
BPD Type 4 Meeting

A BPD Type 4 meeting is a presubmission meeting to discuss the format and content of a
complete application for an original biosimilar or interchangeable product application or
supplement submitted under 351(k) of the PHS Act. The purpose of this meeting is to discuss
the format and content of the planned submission and other items, including the following:

IV.

•

Identification of those studies that the sponsor is relying on to support a demonstration of
biosimilarity or interchangeability

•

Discussion of any potential review issues identified based on the information provided

•

Identification of the status of ongoing or needed studies to adequately address the
Pediatric Research Equity Act

•

Acquainting FDA reviewers with the general information to be submitted in the
marketing application (including technical information)

•

Discussion of the best approach to the presentation and formatting of data in the
marketing application

BSUFA FEES ASSOCIATED WITH THE BPD PROGRAM

Under the BsUFA user fee provisions of the FD&C Act, BPD fees are assessed for products in
the BPD program. BPD fees include the initial BPD fee, the annual BPD fee, and the
reactivation fee. No fee is associated with a BIA meeting. For more information about BsUFA
fees, including the assessment of BPD fees and the consequences for failure to pay any required
BPD fees, refer to the draft guidance for industry Assessing User Fees Under the Biosimilar
User Fee Amendments of 2017. 8

V.

MEETING FORMATS

There are three formats for formal meetings: face to face, teleconference/videoconference, and
WRO as follows:
1. Face to face — Traditional face-to-face meetings are those in which the majority of
attendees participate in person at the FDA.

8

When finalized, this guidance will represent the FDA’s current thinking on this topic.

5

Contains Nonbinding Recommendations
Draft — Not for Implementation

198
199
200
201
202
203
204
205
206
207
208
209
210
211
212
213
214
215
216
217
218
219
220
221
222
223
224
225
226
227
228
229
230
231
232
233
234
235
236
237

2. Teleconference/Videoconference — Teleconferences/videoconferences are meetings in
which the attendees participate from various remote locations via an audio (e.g.,
telephone) and/or video connection.
3. Written response only (WRO) — WRO responses are sent to requesters in lieu of
meetings conducted in one of the other two formats described above. Requesters may
request this meeting format for BIA and BPD Type 2 meetings.

VI.

MEETING REQUESTS

To make the most efficient use of FDA resources, before seeking a meeting, requesters should
consult the information publicly available from the FDA that relates to biosimilar or
interchangeable product development. 9
To promote efficient meeting management, requesters should try to anticipate future needs and,
to the extent practical, combine related product development issues into the fewest possible
meetings.
To request a meeting, submit a written request to the FDA via the respective center’s document
room (paper submissions) or via the electronic gateway, as appropriate. Written meeting
requests must be made in accordance with any applicable electronic submission requirements. 10
Requests should be addressed to the appropriate review division or office and, if previously
assigned, submitted to the pre-investigational new drug application (pre-IND) file or application
(e.g., investigational new drug application (IND), BLA). Meeting requests sent by fax or email
are considered courtesy copies only and are not a substitute for a formal submission.
A meeting request for the development of a proposed biosimilar or interchangeable product with
multiple indications that span multiple review divisions should be submitted to the division that
has regulatory oversight of the reference product.
The meeting request should include adequate information for the FDA to assess the potential
utility of the meeting and to identify FDA staff necessary to discuss proposed agenda items.
The meeting request should include the following information:
1. The application number (if previously assigned).
2. The development-phase code name of product (if pre-licensure).

9

See the guidance for industry Best Practices for Communication Between IND Sponsors and FDA During Drug
Development.

10

See the guidances for industry Providing Regulatory Submissions in Electronic Format — Submissions Under
Section 745A(a) of the Federal Food, Drug, and Cosmetic Act and Providing Regulatory Submissions in Electronic
Format — Certain Human Pharmaceutical Product Applications and Related Submissions Using the eCTD
Specifications.

6

Contains Nonbinding Recommendations
Draft — Not for Implementation

238
239
240
241
242
243
244
245
246
247
248
249
250
251
252
253
254
255
256
257
258
259
260
261
262
263
264
265
266
267
268
269
270
271
272
273
274
275
276
277
278
279
280
281
282

3. The proper name (if post-licensure).
4. The structure (if applicable).
5. The reference product proper and proprietary names.
6. The proposed indication(s) or context of product development.
7. Pediatric study plans, if applicable.
8. Human factors engineering plan, if applicable.
9. Combination product information (e.g., constituent parts, including details of the device
constituent part, intended packaging, planned human factors studies), if applicable.
The meeting request must include the following information for the performance goals described
in section I.I., Meeting Management Goals, of the commitment letter to apply: 11
1. The meeting type being requested (i.e., BIA meeting, BPD Type 1, 2, 3, or 4 meeting).
The rationale for requesting the meeting type should also be included.
2. The proposed format of the meeting (i.e., face to face, teleconference/videoconference or
WRO).
3. A brief statement of the purpose of the meeting. This statement should include a brief
background of the issues underlying the agenda. It also can include a brief summary of
completed or planned studies or data that the requester intends to discuss at the meeting,
the general nature of the critical questions to be asked, and where the meeting fits in
overall development plans. Although the statement should not provide the details of
study designs or completed studies, it should provide enough information to facilitate
understanding of the issues, such as a small table that summarizes major results.
4. A list of the specific objectives or outcomes the requester expects from the meeting.
5. A proposed agenda, including estimated times needed for discussion of each agenda item.
6. A list of questions, grouped by FDA discipline. For each question there should be a brief
explanation of the context and purpose of the question.
7. A list of planned attendees from the requester’s organization, which should include their
names and titles. The list should also include the names, titles, and affiliations of
consultants and interpreters, if applicable.
8. A list of requested FDA attendees and/or discipline representative(s). Note that requests
for attendance by FDA staff who are not otherwise essential to the application’s review
11

See BsUFA II goals letter.

7

Contains Nonbinding Recommendations
Draft — Not for Implementation

283
284
285
286
287
288
289
290
291
292
293
294
295
296
297
298
299
300
301
302
303
304
305
306
307
308
309
310
311
312
313
314
315
316
317
318
319
320
321
322
323
324
325
326
327
328

may affect the ability to hold the meeting within the specified time frame of the meeting
type being requested. Therefore, when attendance by nonessential FDA staff is
requested, the meeting request should provide a justification for such attendees and state
whether or not a later meeting date is acceptable to the requester to accommodate the
nonessential FDA attendees.
9. Suggested dates and times (e.g., morning or afternoon) for the meeting that are within or
beyond the appropriate scheduling time frame of the meeting type being requested (see
Table 2 in section VII.B., Meeting Granted). Dates and times when the requester is not
available should also be included.
When submitting a meeting request, the requester should define the specific areas of input
needed from the FDA. A well-written meeting request that includes the above components can
help the FDA understand and assess the utility and timing of the meeting related to product
development or review. The list of requester attendees and the list of requested FDA attendees
can be useful in providing or preparing for the input needed at the meeting. However, during the
time between the request and the meeting, the planned attendees can change. If there are
changes, an updated list of attendees with their titles and affiliations should be provided to the
appropriate FDA contact at least 1 week before the meeting.
The objectives and agenda provide overall context for the meeting topics, but it is the list of
questions that is most critical to understanding the kind of information or input needed by the
requester and to focus the discussion should the meeting be granted. Each question should be
precise and include a brief explanation of the context and purpose of the question. The questions
submitted within a single meeting request should be limited to those that can be reasonably
answered within the allotted meeting time, taking into consideration the complexity of the
questions submitted. Similar considerations regarding the complexity of questions submitted
within a WRO should be applied.

VII.

ASSESSING AND RESPONDING TO MEETING REQUESTS

Although requesters should request a specific meeting type and format, the FDA assesses each
meeting request, including WRO requests for BIA and BPD Type 2 meetings, and determines
whether or not the request should be granted, the appropriate meeting type, and the appropriate
meeting format. Requests for BPD Type 2, 3, and 4 meetings will be honored except in the most
unusual circumstances. However, if the FDA determines that WRO format is not appropriate for
a requested WRO meeting or that in-person format (i.e., face to face or
teleconference/videoconference) is not appropriate for a requested in-person meeting, we will
notify the requester that the meeting has been denied, as described in section VII.A., Meeting
Denied.
The meeting request should be accompanied by the meeting package (see section VIII.C.,
Meeting Package Content, for additional information regarding the content of the meeting
package). This ensures that the FDA has adequate information to assess the potential utility of
the meeting and prepare for the meeting. If the meeting package is not submitted to the review

8

Contains Nonbinding Recommendations
Draft — Not for Implementation

329
330
331
332
333
334
335
336
337
338
339
340
341
342
343
344
345
346
347
348
349
350
351
352
353
354
355
356
357
358
359
360
361
362
363
364

division with the meeting request, the FDA will consider the meeting request incomplete and
generally will deny the meeting request.
A.

Meeting Denied

If a meeting request is denied, the FDA will notify the requester in writing according to the
timelines described in Table 1. The notification will include an explanation of the reason for the
denial. Denials will be based on a substantive reason, not merely on the absence of a minor
element of the meeting request or a minor element of the meeting package. For example, a
meeting request can be denied because it is premature for the stage of product development, is
clearly unnecessary, or is not appropriate for the format requested (e.g., face to
face/videoconference/teleconference versus WRO) or the meeting package does not provide an
adequate basis for the meeting discussion.
The FDA may also deny requests for meetings that do not have substantive information related
to the elements described in section VI., Meeting Requests. A subsequent request to schedule
the meeting will be considered as a new request (i.e., a request that is assigned a new set of time
frames described below in section VII. B., Meeting Granted).
B.

Meeting Granted

If a meeting request is granted, the FDA will notify the requester in writing according to the
timelines described in Table 1. For face-to-face and teleconference/videoconference meetings,
the notification will include the date, time, conferencing arrangements and/or location of the
meeting, and expected FDA participants. For BIA and BPD Type 2 WRO meetings, the
notification will include the date the FDA intends to send the written response (see Table 3 for
FDA WRO response timelines).
For face-to-face and teleconference/videoconference meetings, the FDA will schedule the
meeting on the next available date at which all expected FDA staff are available to attend;
however, the meeting should be scheduled consistent with the type of meeting requested (see
Table 2 for FDA meeting scheduling time frames). If the requested date for any meeting type is
greater than the specified time frame, the meeting date should be within 14 calendar days of the
requested date.
Table 1: FDA Meeting Request Response Timelines
Response Time
(calendar days from receipt of meeting
Meeting Type
request and meeting package)
BIA
21 days
BPD 1
14 days
BPD 2
21 days
BPD 3
21 days
BPD 4
21 days

365
366

9

Contains Nonbinding Recommendations
Draft — Not for Implementation

367

368
369
370

Table 2: FDA Meeting Scheduling Time Frames
Meeting Scheduling
(calendar days from receipt of
Meeting Type
meeting request and meeting
package)
BIA
75 days
BPD 1
30 days
BPD 2
90 days
BPD 3
120 days
BPD 4
60 days

Table 3: FDA WRO Response Timelines
Meeting Type
BIA
BPD 2

371
372
373
374
375
376
377
378
379
380
381
382
383
384
385
386
387
388
389
390
391
392
393

WRO Response Time
(calendar days from receipt of
WRO meeting request and meeting
package)
75 days
90 days

VIII. MEETING PACKAGE
Premeeting preparation is critical for achieving a productive discussion or exchange of
information. Preparing the meeting background package should help the requester focus on
describing its principal areas of interest. The meeting package should provide information
relevant to the discussion topics and enable the FDA to prepare adequately for the meeting.
A.

Timing of Meeting Package Submission

As discussed in section VII., Assessing and Responding to Meeting Requests, if the meeting
package is not submitted with the meeting request for each meeting type, the meeting request
will be considered incomplete and the FDA generally will deny the meeting.
B.

Where and How Many Copies of Meeting Packages to Send

Requesters should submit an archival meeting package to the appropriate review division or
office or, if previously assigned, to the relevant pre-IND file or application(s) (e.g., IND, BLA)
via the appropriate center’s document room (paper submission) or via the electronic gateway, as
applicable. Submissions must be made in accordance with any applicable electronic submission
requirements. 12

12

See the guidances for industry Providing Regulatory Submissions in Electronic Format — Submissions Under
Section 745A(a) of the Federal Food, Drug, and Cosmetic Act and Providing Regulatory Submissions in Electronic
Format — Certain Human Pharmaceutical Product Applications and Related Submissions Using the eCTD
Specifications.

10

Contains Nonbinding Recommendations
Draft — Not for Implementation

394
395
396
397
398
399
400
401
402
403
404
405
406
407
408
409
410
411
412
413
414
415
416
417
418
419
420
421
422
423
424
425
426
427
428
429
430
431
432
433
434
435
436

To facilitate the meeting process, CDER strongly suggests that copies of meeting packages
provided in electronic format also be provided in paper (desk copies). The number of desk
copies of a meeting package will vary based on the meeting. The CDER project manager will
advise on the number of desk copies needed for the meeting attendees. CBER neither requests
nor accepts paper copies (desk copies) of meeting packages that have been submitted in
electronic format.
C.

Meeting Package Content

The meeting package should provide information relevant to the product, stage of development,
and meeting type requested (see section III., Meeting Types), in addition to any supplementary
information needed to develop responses to issues raised by the requester or review division.
The meeting package should contain sufficient detail to meet the intended meeting objectives.
For example, inclusion of raw data in addition to the derived conclusions may be appropriate in
some situations. Similarly, merely describing a result as significant does not provide the review
division with enough information to give good advice or identify important problems the
requester may have missed. FDA guidances identify and address many issues related to
biosimilar or interchangeable product development and should be considered when planning,
developing, and providing information needed to support a meeting with the FDA. 13 If a product
development plan deviates from current guidances, or from current practices, the deviation
should be recognized and explained. Known or expected difficult design and evidence issues
should be raised for discussion (e.g., selection of study populations, doses, or endpoints different
from those studied for the reference product’s licensure; extrapolation of indications).
To facilitate FDA review, the meeting package content should be organized according to the
proposed agenda. The meeting package should be a sequentially paginated document with a
table of contents, appropriate indices, appendices, and cross references. It should be tabbed or
bookmarked to enhance reviewers’ navigation across different sections within the package, both
in preparation for and during the meeting. Meeting packages generally should include the
following information in the order listed below:
1. The application number (if previously assigned).
2. The development-phase code name of product (if pre-licensure).
3. The proper name (if post-licensure).
4. The structure (if applicable).
5. The reference product proprietary and proper names.
6. The proposed indication(s) or context of product development.

13

See the FDA Biosimilars guidance web page, available at
https://www.fda.gov/Drugs/GuidanceComplianceRegulatoryInformation/Guidances/ucm290967.htm.

11

Contains Nonbinding Recommendations
Draft — Not for Implementation

437
438
439
440
441
442
443
444
445
446
447
448
449
450
451
452
453
454
455
456
457
458
459
460
461
462
463
464
465
466
467
468
469
470
471
472
473
474
475
476
477
478
479
480
481
482

7. The dosage form, route of administration, dosing regimen (frequency and duration), and
presentation(s).
8. Pediatric study plans, if applicable.
9. Human factors engineering plan, if applicable.
10. Combination product information (e.g., constituent parts, including details of the device
constituent part, intended packaging, planned human factors studies), if applicable.
11. A list of all individuals, with their titles and affiliations, who will attend the requested
meeting from the requester’s organization, including consultants and interpreters, if
applicable.
12. A background section that includes the following:
a. A brief history of the development program and relevant communications with the
FDA before the meeting
b. Substantive changes in product development plans (e.g., manufacturing changes, new
study population or endpoint), when applicable
c. The current status of product development (e.g., chemistry, manufacturing, and
controls; nonclinical; and clinical, including any development outside the United
States, as applicable)
13. A brief statement summarizing the purpose of the meeting.
14. A proposed agenda, including estimated times needed for discussion of each agenda item.
15. A list of questions for discussion grouped by FDA discipline and with a brief summary
for each question to explain the need or context for the question. Questions regarding
combination product issues should be grouped together.
16. Data to support discussion organized by FDA discipline and question. The level of detail
of the data should be appropriate to the meeting type requested and the stage of product
development.

IX.

PRELIMINARY RESPONSES

Communications before the meeting between requesters and the FDA, including preliminary
responses, can serve as a foundation for discussion or as the final meeting responses.
Nevertheless, preliminary responses should not be construed as final unless there is agreement
between the requester and the FDA that additional discussion is not necessary for any question
(i.e., when the meeting is canceled because the requester is satisfied with the FDA’s preliminary

12

Contains Nonbinding Recommendations
Draft — Not for Implementation

483
484
485
486
487
488
489
490
491
492
493
494
495
496
497
498
499
500
501
502
503
504
505
506
507
508
509
510
511
512
513
514
515
516
517
518
519
520
521
522
523
524
525
526
527

responses), or a particular question is considered resolved allowing time for discussion of the
other questions during the meeting. Preliminary responses communicated by the FDA are not
intended to generate the submission of new information or new questions. If a requester
nonetheless provides new data or a revised or new proposal, the FDA may not be able to provide
comments on the new information, and the requester may need to submit a new meeting request
for the FDA to provide feedback on the new information.
The FDA holds internal meetings, including meetings with the CDER or CBER Biosimilar
Review Committee, to discuss the content of meeting packages and to gain internal alignment on
the preliminary responses. The FDA will send the requester its preliminary responses to the
questions in the meeting package no later than 5 calendar days before the face-to-face,
videoconference, or teleconference meeting date for BPD Type 2 and BPD Type 3 meetings.
For all other meeting types, the FDA intends to send the requester its preliminary responses no
later than 2 calendar days before the face-to-face, videoconference, or teleconference meeting.

X.

RESCHEDULING MEETINGS

Occasionally, circumstances arise that necessitate the rescheduling of a meeting. If a meeting
needs to be rescheduled, it should be rescheduled as soon as possible after the original date. A
new meeting request should not be submitted. Requesters and the FDA should take reasonable
steps to avoid rescheduling meetings. For example, if an attendee becomes unavailable, a
substitute can be identified, or comments on the topic that the attendee would have addressed can
be forwarded to the requester following the meeting. It will be at the discretion of the review
division whether the meeting should be rescheduled depending on the specific circumstances.
The following situations are examples of when a meeting may be rescheduled by FDA. This list
includes representative examples and is not intended to be an exhaustive list.
•

The review team determines that additional information is needed to address the
requester’s questions or other important issues, and it is possible to identify the additional
information needed and arrange for its timely submission.

•

Essential attendees are no longer available for the scheduled date and time because of an
unexpected or unavoidable conflict or an emergency situation.

•

Before preliminary responses are sent by the FDA, the requester sends the FDA
additional questions or data that are intended for discussion at the meeting and require
additional review time.

•

It is determined that attendance by additional FDA personnel not originally anticipated or
requested is critical and their unavailability precludes holding the meeting on the original
date.

13

Contains Nonbinding Recommendations
Draft — Not for Implementation

528
529
530
531
532
533
534
535
536
537
538
539
540
541
542
543
544
545
546
547
548
549
550
551
552
553
554
555
556
557
558
559
560
561
562
563
564
565
566
567
568

XI.

CANCELING MEETINGS

Failure to pay required BPD fees for a product, within the required time frame, may result in the
cancellation by FDA of a previously scheduled BPD meeting. 14 For more information on BPD
fees, refer to the draft guidance for industry Assessing User Fees Under the Biosimilar User Fee
Amendments of 2017. 15 If the requester pays the required BPD fee after the meeting has been
canceled because of nonpayment, the goal time frame for FDA’s response to a meeting request
will be calculated from the date on which FDA received the payment, not the date on which the
sponsor originally submitted the meeting request. 16
Occasionally, other circumstances arise that necessitate the cancellation of a meeting. If a
meeting is canceled for reasons other than nonpayment of a required BPD fee, the FDA will
consider a subsequent request to schedule a meeting to be a new request and the goal time frame
for FDA’s response will be calculated from the date of the subsequent request. Requesters and
the FDA should take reasonable steps to avoid canceling meetings (unless the meeting is no
longer necessary). Cancellation will be at the discretion of the review division and will depend
on the specific circumstances.
The following situations are examples of when a meeting may be canceled. This list includes
representative examples and is not intended to be an exhaustive list.
•

The requester determines that preliminary responses to its questions are sufficient for its
needs and additional discussion is not necessary (see section IX., Preliminary Responses).
In this case, the requester should contact the FDA regulatory project manager to request
cancellation of the meeting. The FDA will consider whether it agrees that the meeting
should be canceled. Some meetings can be valuable because of the discussion they
generate and the opportunity for the division to ask about relevant matters, even if the
preliminary responses seem sufficient to answer the requester’s questions. If the FDA
agrees that the meeting can be canceled, the reason for cancellation will be documented
and the preliminary responses will represent the final responses and the official record.

•

The FDA determines that the meeting package is inadequate. Meetings are scheduled on
the condition that the requester has submitted appropriate information to support the
discussion. Adequate planning by the requester should avoid this problem.

XII.

MEETING CONDUCT

Meetings will be chaired by an FDA staff member and begin with introductions and an overview
of the agenda. Attendees should not make audio or visual recordings of discussions at meetings
described in this guidance.
14

See section 744H(a)(1)(E)(i) of the FD&C Act.

15

When finalized, this guidance will represent the FDA’s current thinking on this topic.

16

See BsUFA II goals letter.

14

Contains Nonbinding Recommendations
Draft — Not for Implementation

569
570
571
572
573
574
575
576
577
578
579
580
581
582
583
584
585
586
587
588
589
590
591
592
593
594
595
596
597
598
599
600
601
602
603
604
605
606
607
608
609
610
611
612

Presentations by requesters generally are not needed because the information necessary for
review and discussion should be part of the meeting package. If a requester plans to make a
presentation, the presentation should be discussed ahead of time with the FDA project manager
to determine if a presentation is warranted and to ensure that the FDA has the presentation
materials ahead of the meeting, if possible. All presentations should be kept brief to maximize
the time available for discussion. The length of the meeting will not be increased to
accommodate a presentation. If a presentation contains more than a small amount of content,
distinct from clarifications or explanations of previous data, that was not included in the original
meeting package submitted for review, FDA staff may not be able to provide commentary.
Either a representative of the FDA or the requester should summarize the important discussion
points, agreements, clarifications, and action items. Summation can be done at the end of the
meeting or after the discussion of each question. Generally, the requester will be asked to
present the summary to ensure that there is mutual understanding of meeting outcomes and
action items. FDA staff can add or further clarify any important points not covered in the
summary and these items can be added to the meeting minutes.
At BPD Type 4 meetings for original applications reviewed under the BsUFA Program for
Enhanced Review Transparency and Communication for Original 351(k) BLAs (also known as
the Program), 17 the requester and the FDA should also summarize agreements regarding the
content of a complete application and any agreements reached on delayed submission of certain
minor application components.

XIII. MEETING MINUTES
Because the FDA’s minutes are the official records of meetings, the FDA’s documentation of
meeting outcomes, agreements, disagreements, and action items is critical to ensuring that this
information is preserved for meeting attendees and future reference. The FDA will issue the
official, finalized minutes to the requester within 30 calendar days after the meeting.
The following are general considerations regarding meeting minutes:

17

•

FDA minutes will outline the important agreements, disagreements, issues for further
discussion, and action items from the meeting in bulleted format. This information does
not need to be in great detail. The minutes are not intended to represent a transcript of
the meeting.

•

FDA project managers will use established templates to ensure that all important meeting
information is captured.

•

The FDA may communicate additional information in the final minutes that was not
explicitly communicated during the meeting (e.g., pediatric requirements, data standards)

See BsUFA II goals letter.

15

Contains Nonbinding Recommendations
Draft — Not for Implementation

613
614
615
616
617
618
619
620
621
622
623
624
625
626
627
628
629
630
631
632
633
634
635
636
637
638
639
640
641
642
643
644
645

or that provides further explanation of discussion topics. The FDA’s final minutes will
distinguish this additional information from the discussion that occurred during the
meeting.
The following steps should be taken when a requester disagrees that the minutes are an accurate
account of the meeting:
•

The requester should contact the FDA project manager and describe the concern

•

If, after contacting the FDA project manager, the requester still disagrees with the content
of the minutes, the requester should submit a description of the specific disagreements
either:

•

‒

To the application; or

‒

If there is no application, in a letter to the division director, with a copy to the FDA
project manager

The review division and the office director, if the office director was present at the
meeting, will take the concerns under consideration
‒

If the minutes are deemed to accurately and sufficiently reflect the meeting
discussion, the FDA project manager will convey this decision to the requester and
the minutes will stand as the official documentation of the meeting.

‒

If the FDA deems it necessary, changes will be documented in an addendum to the
official minutes. The addendum will also document any remaining requester
objections.

To request information on additional issues that were not addressed at the meeting, the requester
should submit a new meeting request or a submission containing specific questions for FDA
feedback.

16

Contains Nonbinding Recommendations
Draft — Not for Implementation

646
647
648
649
650
651
652
653
654
655
656
657
658
659
660
661
662
663
664
665
666
667
668
669
670
671
672
673
674
675
676
677
678

REFERENCES
Related guidances 1
Draft guidance for industry Assessing User Fees Under the Biosimilar User Fee Amendments of
2017 2
Guidance for industry and review staff Best Practices for Communication Between IND
Sponsors and FDA During Drug Development
Guidance for review staff and industry Good Review Management Principles and Practices for
PDUFA Products
Related CBER SOPPs 3
SOPP 8101.1: Regulatory Meetings With Sponsors and Applicants for Drugs and Biological
Products
SOPP 8404.1: Procedures for Filing an Application When the Applicant Protests a Refusal to
File Action (File Over Protest)
Other guidances
Draft guidance for industry Formal Meetings Between the FDA and Sponsors or Applicants of
PDUFA Products 4
Guidance for industry Providing Regulatory Submissions in Electronic Format — Certain
Human Pharmaceutical Product Applications and Related Submissions Using the eCTD
Specifications
Guidance for industry Providing Regulatory Submissions in Electronic Format — Submissions
Under Section 745A(a) of the Federal Food, Drug, and Cosmetic Act

1
We update guidances periodically. To make sure you have the most recent version of a guidance, check the FDA
Drugs or Biologics guidance web pages at
https://www.fda.gov/Drugs/GuidanceComplianceRegulatoryInformation/Guidances/default.htm and
https://www.fda.gov/BiologicsBloodVaccines/GuidanceComplianceRegulatoryInformation/Guidances/default.htm.
2

When final, this guidance will represent the FDA’s current thinking on this topic. For the most recent version of a
guidance, check the FDA Drugs or Biologics guidance web pages at
https://www.fda.gov/Drugs/GuidanceComplianceRegulatoryInformation/Guidances/default.htm and
https://www.fda.gov/BiologicsBloodVaccines/GuidanceComplianceRegulatoryInformation/Guidances/default.htm.
3

SOPPs can be found on the Biologics Procedures (SOPPs) web page at
https://www.fda.gov/BiologicsBloodVaccines/GuidanceComplianceRegulatoryInformation/ProceduresSOPPs/defau
lt.htm.

4

When final, this guidance will represent the FDA’s current thinking on this topic.

17

Contains Nonbinding Recommendations
Draft — Not for Implementation

679
680
681
682
683

Guidance for industry Special Protocol Assessment
Guidance for industry and review staff Formal Dispute Resolution: Sponsor Appeals Above the
Division Level

18