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ISO 14644-8:2022(en)

ISO 14644-8 is a part of the ISO 14644 series that provides guidelines for the classification of airborne molecular contamination (AMC) in cleanrooms and controlled environments. While other parts of the ISO 14644 series focus on particulate contamination, ISO 14644-8 addresses the control and measurement of molecular contaminants, such as gases, vapors, and chemical compounds, that can affect sensitive processes in industries like pharmaceuticals, semiconductors, and aerospace. This standard provides a framework for evaluating the presence of molecular contaminants that could potentially compromise product quality, performance, or safety. It outlines the methods for measuring and monitoring AMC, as well as offering guidance on how to manage these contaminants through appropriate materials selection, air filtration, and environmental control systems. ISO 14644-8 is particularly important for environments where even low levels of chemical contamination can lead to defects or contamination in highly sensitive manufacturing processes.


ISO-14644-8-2022.pdf


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Foreword

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 209, Cleanrooms and associated controlled environments, in collaboration with the European Committee for Standardization (CEN) Technical Committee CEN/TC 243, Cleanroom technology, in accordance with the Agreement on technical cooperation between ISO and CEN (Vienna Agreement).

This third edition cancels and replaces the second edition (ISO 14644-8:2013), of which it constitutes a minor revision. The changes are as follows:

  •  the term class (classification, classified) changed to grade or assessment where appropriate;

  •  3.1.2, definition revised;

  •  Bibliography updated;

  •  minor editorial changes.

A list of all parts in the ISO 14644 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.

Introduction

Cleanrooms and associated controlled environments provide for the control of airborne particulate contamination to levels of cleanliness appropriate for accomplishing process activities sensitive to a range of contaminants. Products and processes that benefit from the control of airborne contamination include those in such industries as aerospace, microelectronics, pharmaceuticals, medical devices, food, healthcare, optics, instrumentation, vacuum technology, coatings, photovoltaics, displays, LEDs, coatings, automotive and surface analysis.

In some of these industries, the product or process can be sensitive to, or can be destroyed by, chemical contamination resulting from chemicals that are present due to external, process or other generated sources.

Within this document, the presence of chemicals is expressed as air chemical contamination. Chemical contamination is a three-step event. The first step is generation due to external sources such as process leakage, construction material, personnel or material outgassing. The second step is transport as airborne chemical contamination. The third step is sorption on the sensitive surface, which can be quantified as a surface chemical contamination.

The generating materials and the surfaces where sorption takes place will have a large influence on the steps of generation and sorption in addition to the actual air contamination. Thus, for these two steps, not only the contaminants but also the involved bulk and surfaces need to be defined. In order to make a standard generally applicable to any type of cleanroom or associated controlled environment, air chemical cleanliness (ACC) has been chosen for the level assessment.

This document assigns ISO grading levels to be used to specify the level of ACC within a cleanroom and associated controlled environment, where the product or process is deemed to be at risk from air chemical contamination.

For level assessment purposes, this document provides guidance for a range of ACC levels and provides standard protocols for specifying such levels with regard to chemical compounds, methods of test and analysis, and time weighted factors.

Annexes A to D contain the following information:

  •  parameters for consideration: Annex A;

  •  typical contaminating chemicals and substances: Annex B;

  •  typical methods of measurement and analysis: Annex C;

  •  considerations of specific requirements for separative devices: Annex D.

This document is one of a series of standards concerned with cleanrooms and contamination control. Many factors besides ACC need to be considered in the design, specification, operation and control of cleanrooms and other controlled environments. These features are recognized in this document and covered in some detail in other parts of the International Standards prepared by ISO/TC 209, including the ISO 14698 series. In some circumstances, relevant regulatory agencies can impose supplementary policies or restrictions. In such situations, appropriate adaptations of this document can be required.

NOTE When assessment of ACC at critical control point(s) is used as an additional cleanliness attribute to classification of air cleanliness by airborne particle concentration in accordance with ISO 14644-1, then the space can be described as a cleanroom or clean-zone. If ACC is used alone, then the space must be described as a controlled zone.

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ISO 14644-8:2022(EN) Video Introduction

FAQ

  • Q: What is ISO 14644-1 Class 8 standards?

    A: ISO 14644-1 Class 8 refers to the cleanliness standard for cleanrooms based on the maximum allowable concentration of airborne particles of size 0.5 microns or larger. According to ISO 14644-1, an ISO Class 8 cleanroom allows a maximum of 3,520,000 particles per cubic meter of air that are 0.5 microns or larger. This class of cleanroom is considered suitable for less sensitive environments where contamination control is important but not as critical as higher-class rooms (e.g., Class 5 or Class 7). ISO Class 8 cleanrooms are commonly used in industries such as food processing, non-critical medical device manufacturing, and some areas of pharmaceuticals, where the risk of contamination is managed but does not require the strictest control of airborne particles.


  • Q: What is the difference between ISO 14698 and ISO 14644?

    A: ISO 14644 and ISO 14698 are both part of the standards for cleanrooms, but they focus on different aspects of contamination control. ISO 14644 is primarily concerned with cleanroom classification based on airborne particulate contamination (such as particle count and air cleanliness standards), and it defines the cleanliness levels for various cleanroom classes (e.g., Class 1 to Class 9). In contrast, ISO 14698 focuses on biological contamination control, particularly the microbiological testing of cleanrooms, such as methods for testing the presence of bacteria, fungi, and other microorganisms. ISO 14644 provides guidelines for physical contamination, while ISO 14698 focuses on microbial contamination, offering guidelines for the monitoring and control of biocontaminants in controlled environments.


  • Q: What is an ISO Class 8 cleanroom?

    A: An ISO Class 8 cleanroom is a type of controlled environment that meets specific cleanliness criteria based on the concentration of airborne particles. According to the ISO 14644-1 standard, an ISO Class 8 cleanroom allows a maximum of 3,520,000 particles of 0.5 microns or larger per cubic meter of air. While this is a less stringent classification compared to higher-class rooms (such as Class 7 or Class 5), it is still suitable for environments that require some level of contamination control, like certain manufacturing processes in pharmaceuticals, packaging, food processing, or electronic assembly. The primary purpose of an ISO Class 8 cleanroom is to minimize contamination risks in applications where high precision or sterility is not as critical as in more controlled environments like those for semiconductor production or sterile pharmaceutical manufacturing.


  • Q: What is the latest version of ISO 14644?

    A: The latest version of ISO 14644 includes several updated parts, with the most recent revisions being ISO 14644-1:2015, ISO 14644-2:2015, ISO 14644-3:2019, ISO 14644-4:2018, and ISO 14644-5:2020. These versions reflect current best practices in cleanroom classification, testing, monitoring, and environmental control. ISO 14644-1:2015 outlines the classification of cleanrooms based on airborne particle concentrations, while ISO 14644-2:2015 provides procedures for monitoring cleanroom performance. ISO 14644-3:2019 deals with testing methods for measuring particle counts, airflow, and other factors, and ISO 14644-4:2018 focuses on the air change rates and airflow patterns necessary to maintain cleanroom standards. ISO 14644-5:2020 provides guidelines on the installation, maintenance, and verification of cleanroom equipment. These revisions help ensure that cleanrooms meet stringent contamination control requirements across industries such as pharmaceuticals, biotechnology, and semiconductor manufacturing.

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