ISO 13926-3:2019
(Main)Pen systems - Part 3: Seals for pen-injectors for medical use
Pen systems - Part 3: Seals for pen-injectors for medical use
This document specifies the shape, dimensions, material, performance requirements and labelling of seals for pen-injectors for medical use. NOTE The potency, purity, stability and safety of a medicinal product during its manufacture and storage can be significantly affected by the nature and performance of the primary packaging.
Systèmes de stylos-injecteurs — Partie 3: Joints pour stylos-injecteurs à usage médical
General Information
- Status
- Published
- Publication Date
- 26-May-2019
- Current Stage
- 9093 - International Standard confirmed
- Start Date
- 15-Oct-2024
- Completion Date
- 13-Dec-2025
Relations
- Effective Date
- 15-Dec-2017
Overview
ISO 13926-3:2019 - Pen systems - Part 3: Seals for pen-injectors for medical use specifies the shape, dimensions, materials, performance requirements and labelling for seals used in pen‑injectors. It focuses on the primary‑packaging seal (aluminium cap + elastomeric disc) whose properties can materially affect the potency, purity, stability and safety of medicinal products during manufacture and storage.
Key topics and requirements
- Scope and classification
- Applies to seals for pen‑injectors; seals are classified as Type A (mono‑layer disc) or Type B (double‑layer disc).
- Shape and dimensions
- Standardised cap and disc geometries and tolerances are given (nominal sizes and dimensional rules); surface structuring is allowed to avoid sticking.
- Materials
- Caps: aluminium caps must conform to ISO 8872 and be anodized or suitably coated.
- Discs: elastomeric formulations must be the type originally tested and approved by the end user; manufacturers must ensure conformance to the agreed type sample.
- Elastomeric discs shall withstand two autoclave cycles at 121 ± 2 °C for 30 min without functional impairment (other sterilization methods must be evaluated).
- Physical performance
- Hardness: agreement between manufacturer and user; typical tolerance ±5 Shore A (or ±5 IRHD when applicable).
- Fragmentation: testing per ISO 8871‑5 using a medical needle (reference to ISO 7864).
- Freedom from leakage: mandatory leakage test (normative Annex A) using water‑filled cartridges and a defined force applied for a set time interval.
- Resealability: requirements reference ISO 11608‑3.
- Resistance to ageing: seals must maintain performance over the medicinal product’s shelf life (storage guidance per ISO 2230).
- Chemical and biological
- Chemical extractables and biological requirements reference ISO 8871‑1 and ISO 8871‑4 respectively.
- Labelling and designation
- Standard designation format e.g. “Seal ISO 13926‑3 – 7,5 – A”.
Practical applications and users
ISO 13926‑3 is intended for:
- Medical device and pen‑injector manufacturers (design and production)
- Pharmaceutical companies specifying primary packaging for injectable drugs (e.g., insulin pens)
- Elastomer and cap suppliers for qualification and incoming inspection
- Quality assurance, regulatory affairs and procurement teams for supplier agreements and stability programs
- Test houses validating leakage, resealability, sterilization compatibility and ageing
Using this standard helps ensure component interchangeability, product safety, compatibility with sterilization processes and consistent performance over shelf life.
Related standards
Relevant referenced documents include: ISO 13926‑1, ISO 13926‑2, ISO 8871 (parts 1,4,5), ISO 8872, ISO 11608‑3, ISO 48‑4, ISO 7864, ISO 15378, ISO 2230.
Keywords: ISO 13926-3:2019, seals for pen-injectors, pen systems, elastomeric seals, leakage test, resealability, medical device packaging, pharmaceutical primary packaging.
Frequently Asked Questions
ISO 13926-3:2019 is a standard published by the International Organization for Standardization (ISO). Its full title is "Pen systems - Part 3: Seals for pen-injectors for medical use". This standard covers: This document specifies the shape, dimensions, material, performance requirements and labelling of seals for pen-injectors for medical use. NOTE The potency, purity, stability and safety of a medicinal product during its manufacture and storage can be significantly affected by the nature and performance of the primary packaging.
This document specifies the shape, dimensions, material, performance requirements and labelling of seals for pen-injectors for medical use. NOTE The potency, purity, stability and safety of a medicinal product during its manufacture and storage can be significantly affected by the nature and performance of the primary packaging.
ISO 13926-3:2019 is classified under the following ICS (International Classification for Standards) categories: 11.040.25 - Syringes, needles an catheters. The ICS classification helps identify the subject area and facilitates finding related standards.
ISO 13926-3:2019 has the following relationships with other standards: It is inter standard links to ISO 13926-3:2012. Understanding these relationships helps ensure you are using the most current and applicable version of the standard.
You can purchase ISO 13926-3:2019 directly from iTeh Standards. The document is available in PDF format and is delivered instantly after payment. Add the standard to your cart and complete the secure checkout process. iTeh Standards is an authorized distributor of ISO standards.
Standards Content (Sample)
INTERNATIONAL ISO
STANDARD 13926-3
Second edition
2019-05
Pen systems —
Part 3:
Seals for pen-injectors for medical use
Systèmes de stylos-injecteurs —
Partie 3: Joints pour stylos-injecteurs à usage médical
Reference number
©
ISO 2019
© ISO 2019
All rights reserved. Unless otherwise specified, or required in the context of its implementation, no part of this publication may
be reproduced or utilized otherwise in any form or by any means, electronic or mechanical, including photocopying, or posting
on the internet or an intranet, without prior written permission. Permission can be requested from either ISO at the address
below or ISO’s member body in the country of the requester.
ISO copyright office
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Phone: +41 22 749 01 11
Fax: +41 22 749 09 47
Email: copyright@iso.org
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Published in Switzerland
ii © ISO 2019 – All rights reserved
Contents Page
Foreword .iv
Introduction .v
1 Scope . 1
2 Normative references . 1
3 Terms and definitions . 1
4 Classification . 2
5 Shape and dimensions . 2
6 Designation . 3
7 Material . 3
7.1 Cap . 3
7.2 Disc . 3
8 Requirements . 3
8.1 General . 3
8.2 Physical requirements . 3
8.2.1 Hardness of the disc . 3
8.2.2 Fragmentation . 4
8.2.3 Freedom from leakage . 4
8.2.4 Resealability . . 4
8.2.5 Resistance to ageing . 4
8.3 Chemical requirements. 4
8.4 Biological requirements . 4
9 Labelling . 4
Annex A (normative) Leakage test . 5
Bibliography . 7
Foreword
ISO (the International Organization for Standardization) is a worldwide federation of national standards
bodies (ISO member bodies). The work of preparing International Standards is normally carried out
through ISO technical committees. Each member body interested in a subject for which a technical
committee has been established has the right to be represented on that committee. International
organizations, governmental and non-governmental, in liaison with ISO, also take part in the work.
ISO collaborates closely with the International Electrotechnical Commission (IEC) on all matters of
electrotechnical standardization.
The procedures used to develop this document and those intended for its further maintenance are
described in the ISO/IEC Directives, Part 1. In particular, the different approval criteria needed for the
different types of ISO documents should be noted. This document was drafted in accordance with the
editorial rules of the ISO/IEC Directives, Part 2 (see www .iso .org/directives).
Attention is drawn to the possibility that some of the elements of this document may be the subject of
patent rights. ISO shall not be held responsible for identifying any or all such patent rights. Details of
any patent rights identified during the development of the document will be in the Introduction and/or
on the ISO list of patent declarations received (see www .iso .org/patents).
Any trade name used in this document is information given for the convenience of users and does not
constitute an endorsement.
For an explanation of the voluntary nature of standards, the meaning of ISO specific terms and
expressions related to conformity assessment, as well as information about ISO's adherence to the
World Trade Organization (WTO) principles in the Technical Barriers to Trade (TBT) see www .iso
.org/iso/foreword .html.
This document was prepared by Technical Committee ISO/TC 76, Transfusion, infusion and injection, and
blood processing equipment for medical and pharmaceutical use.
This second edition cancels and replaces the first edition (ISO 13926-3:2012), which has been
technically revised. The main changes compared to the previous edition are as follows:
— extension of the nature of cap in 7.1;
— deletion of one reference to a minimum requirement in 8.1;
— change of the reference in 8.2.2 to a needle for medical use;
— complete editorial revision.
A list of all parts in the ISO 13926 series can be found on the ISO website.
Any feedback or questions on this document should be directed to the user’s national standards body. A
complete listing of these bodies can be found at www .iso .org/members .html.
iv © ISO 2019 – All rights reserved
Introduction
Primary packaging components made of elastomeric materials are an integral part of medicinal
products. As such, the principles of current Good Manufacturing Practices (cGMP) are applicable to the
manufacturing of these components.
Principles of cGMP are described, for example, in ISO 15378.
INTERNATIONAL STANDARD ISO 13926-3:2019(E)
Pen systems —
Part 3:
Seals for pen-injectors for medical use
1 Scope
This document specifies the shape, dimensions, material, performance requirements and labelling of
seals for pen-injectors for medic
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