ISO/TR 19244:2014
(Main)Guidance on transition periods for standards developed by ISO/TC 84 - Devices for administration of medicinal products and catheters
Guidance on transition periods for standards developed by ISO/TC 84 - Devices for administration of medicinal products and catheters
ISO/TR 19244:2014 outlines the recommended transition plans for all the TC 84 standards: Needle-based Injection systems; Sharps Injury Protection; Sharps Containers, Aerosol Drug Delivery Devices; Needle-free injection systems; Syringes; Needles; Intravascular Catheters and Ports.
Directives relatives aux périodes de transition concernant les normes développées par l'ISO/TC 84 — Dispositifs d'administration de produits médicinaux et cathéters
General Information
- Status
- Published
- Publication Date
- 06-Aug-2014
- Technical Committee
- ISO/TC 84 - Devices for administration of medicinal products and catheters
- Current Stage
- 6060 - International Standard published
- Start Date
- 07-Aug-2014
- Completion Date
- 01-Aug-2014
Overview
ISO/TR 19244:2014 - Guidance on transition periods for standards developed by ISO/TC 84 - provides recommended transition plans for standards covering devices for administration of medicinal products and intravascular catheters. It clarifies how manufacturers, notified bodies and regulators should treat new or revised ISO/TC 84 standards from the date of publication, addressing concepts such as grandfathering, transition period, and significant design change.
Key topics and requirements
- Scope: Applies across ISO/TC 84 series, including needle-based injection systems, sharps protection and containers, aerosol drug delivery, needle-free injectors, syringes, needles, intravascular catheters and ports.
- Grandfathering (marketed devices):
- Marketed devices that show acceptable post-market safety/performance may remain on the market without meeting the newest standard.
- Conditions: adequate post-market data and an annual updated risk assessment (see ISO 14971).
- If a device undergoes a significant design change, grandfathering should not apply and design verification to the latest standard is recommended.
- Non-marketed and new devices:
- Recommended that non-marketed devices be designed to the latest edition.
- New marketed devices should comply with the new standard no later than three years after publication; beyond that, regulators or notified bodies should not accept conformity claims referencing the previous version.
- Rationale:
- Transition periods allow time for test method development, validation, documentation updates, and regulatory approval coordination with Notified Bodies and Competent Authorities.
Practical applications
- Provides a clear, pragmatic approach for:
- Regulatory affairs teams planning conformity timelines after publication of a revised ISO/TC 84 standard.
- Product development and quality engineers performing design verification and validation.
- Risk managers conducting annual ISO 14971-based assessments to justify grandfathering.
- Notified Bodies and Competent Authorities assessing acceptance of legacy devices and design changes.
Who should use this standard
- Medical device manufacturers (R&D, QA/RA)
- Regulatory and compliance professionals
- Notified Bodies and auditors
- Design verification and validation teams
- Risk management specialists
Related standards
Key referenced documents include:
- ISO 11608 (needle-based injection systems)
- ISO 20072 (aerosol drug delivery)
- ISO 21649 (needle-free injectors)
- ISO 7886 / ISO 8537 / ISO 9626 (syringes and needle components)
- ISO 23907 / ISO 23908 (sharps protection)
- ISO 10555 / ISO 11070 (intravascular catheters and introducers)
- ISO 14971 (risk management)
Keywords: ISO/TR 19244:2014, ISO/TC 84, transition periods, grandfathering, medical devices, administration of medicinal products, catheters, design verification, notified body, risk assessment.
Frequently Asked Questions
ISO/TR 19244:2014 is a technical report published by the International Organization for Standardization (ISO). Its full title is "Guidance on transition periods for standards developed by ISO/TC 84 - Devices for administration of medicinal products and catheters". This standard covers: ISO/TR 19244:2014 outlines the recommended transition plans for all the TC 84 standards: Needle-based Injection systems; Sharps Injury Protection; Sharps Containers, Aerosol Drug Delivery Devices; Needle-free injection systems; Syringes; Needles; Intravascular Catheters and Ports.
ISO/TR 19244:2014 outlines the recommended transition plans for all the TC 84 standards: Needle-based Injection systems; Sharps Injury Protection; Sharps Containers, Aerosol Drug Delivery Devices; Needle-free injection systems; Syringes; Needles; Intravascular Catheters and Ports.
ISO/TR 19244:2014 is classified under the following ICS (International Classification for Standards) categories: 11.040.01 - Medical equipment in general. The ICS classification helps identify the subject area and facilitates finding related standards.
You can purchase ISO/TR 19244:2014 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)
TECHNICAL ISO/TR
REPORT 19244
First edition
2014-08-15
Guidance on transition periods for
standards developed by ISO/TC
84 — Devices for administration of
medicinal products and catheters
Directives relatives aux périodes de transition concernant les normes
développées par l’ISO/TC 84 — Dispositifs d’administration de
produits médicinaux et cathéters
Reference number
©
ISO 2014
© ISO 2014
All rights reserved. Unless otherwise specified, no part of this publication may be reproduced or utilized otherwise in any form
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the requester.
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Published in Switzerland
ii © ISO 2014 – All rights reserved
Contents Page
Foreword .iv
Introduction .v
1 Scope . 1
2 Terms and definitions . 1
3 Recommendations for implementing ISO/TC 84 standards . 1
3.1 Marketed devices (Grandfathering). 1
3.2 Non-marketed devices. 2
3.3 Rationale for the transition period . 2
Bibliography . 3
Foreword
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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. 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. 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 on the meaning of ISO specific terms and expressions related to conformity
assessment, as well as information about ISO’s adherence to the WTO principles in the Technical Barriers
to Trade (TBT), see the following URL: Foreword - Supplementary information
The committee responsible for this document is ISO/TC 84, Devices for administration of medicinal
products and intravascular catheters.
iv © ISO 2014 – All rights reserved
Introduction
This Technical Report outlines an ISO/TC 84 recommended transition period for newly published
standards. It describes the recommended plan and the rationale for transitioning from “old versions” or
“outdated” standards, which have been updated or replaced by new ISO/TC 84 standards. It addresses
the concepts of “Grandfathering” and “Transition Periods” relative to compliance requirements with
new standards.
When new International Standards are issued, the standard is valid from the date of publication. When
new versions of existing International Standards are issued, the new standard is valid from the date
of publication and the previous version of the standard is wit
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