Container Closure Systems for Packaging Human Drugs and Biologics -- Questions and Answers: Guidance for Industry

Administrative guidance, not enacted legislation. This captured publisher edition preserves the listed document and attachments; later developments are not independently consolidated.

Guidance for Industry
Container Closure Systems for
Packaging Human Drugs
and Biologics
Questions and Answers
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)
May 2002
CMC

Guidance for Industry
Container Closure Systems for
Packaging Human Drugs
and Biologics
Questions and Answers
Additional copies are available from:
Office of Training and Communications
Division of Drug Information, HFD-240
Center for Drug Evaluation and Research
Food and Drug Administration
5600 Fishers Lane
Rockville, MD 20857
(Tel) 301-827-4573
http://www.fda.gov/cder/guidance/index.htm
or
Office of Communication, Training and
Manufacturers Assistance, HFM-40
Center for Biologics Evaluation and Research
Food and Drug Administration
1401 Rockville Pike, Rockville, MD 20852-1448
http://www.fda.gov/cber/guidelines.htm
Fax: 1-888-CBERFAX or 301-827-3844
Phone: the Voice Information System at 800-835-4709 or 301-827-1800
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)
May 2002
CMC

Guidance for Industry1
Container Closure Systems for Packaging
Human Drugs and Biologics
Questions and Answers
This guidance represents the Food and Drug Administration=s current thinking on this topic. It does not
create or confer any rights for or on any person and does not operate to bind FDA or the public. An
alternative approach may be used if such approach satisfies the requirements of the applicable statutes
and regulations.
This document provides questions and answers relating to the guidance on Container Closure
Systems for Packaging Human Drugs and Biologics (the guidance).2 The questions are based on
those posed to CDER by applicants.
Q1: 	Table 5 of the guidance (section III.E.2) provides information on the American
Academy of Ophthalmology (AAO) uniform color coding system for the caps and labels
of topical ocular medications. Is there a source for current information on this coding
system?
A1: 	Current information on the AAO color coding system can be found on AAO’s Web
site at http:///www.aao.org (type color coding in the search entry box).
Q2: 	Section VI.B of the guidance states that container closure systems for on-site storage
have generally been considered a Current Good Manufacturing Practices (CGMP)
issue. However, the guidance goes on to state that if a firm plans to hold bulk drug
products3 in storage, then the container closure system and the maximum storage time
should be described and justified in the application. If this is a CGMP issue, does
information need to be included in the application?
1 This guidance has been prepared by the Packaging Technical Committee of the Chemistry, Manufacturing, and
Controls Committee (CMCCC) in the Center for Drug Evaluation and Research (CDER) at the Food and Drug
Administration (FDA).
2 A notice of availability for this guidance published in the Federal Register on July 7, 1999 (64 FR 36694).
3 A bulk drug product means finished dosage form that has not yet been packaged into the container closure systems
intended for market and/or sale.
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A2: 	Information on container closure systems used for storage of bulk drug products,
other than biologics or protein drug products, need not be included in the application.
However, these container closure systems should be shown to be suitable for their
intended use. The suitability of the storage containers should be supported by data
retained by the applicant and/or manufacturer and should be made available during
FDA inspection upon demand. Information as requested in section VI.B. of the
packaging guidance should be included in the application on the container closure
system for storage prior to packaging or shipping of biologics and protein drug
products, including container closure suitability. This information should be provided
for biologics and proteins because, in general, there is greater potential for adverse
effects on the identity, strength, quality, purity, or potency of biologics and protein
drug products during storage or shipping.
Q3: 	Section VI.B of the guidance states that a container closure system for the
transportation of bulk drug products to contract packagers should be described in the
application; section VI.B also provides recommendations on information to include in
the application. However, different recommendations are provided for holding bulk
drug products in storage, and this situation appears to include shipping of bulk drug
products between applicant-owned manufacturing sites and applicant-owned
packaging sites. Why are the recommendations different for these similar situations?
A3: 	Information on container closure systems used for shipping (i.e., between applicant's
own facilities or contract facilities) and bulk drug products, other than biologics or
proteins, need not be included in the application. However, these container closure
systems should be shown to be suitable for their intended use. The suitability of the
storage containers should be supported by data retained by the applicant and/or
manufacturer and should be made available during FDA inspection upon demand.
Information as requested in section VI.B. of the packaging guidance on the container
closure system for storage (shipping) of biologics and protein drug products,
including container closure suitability, should be included in the application. This
information should be provided for biologics and proteins because, in general, there is
greater potential for adverse effects on the identity, strength, quality, purity, or
potency of biologics and proteins during storage or shipping.
2