ISO 13408-1:2023 PDF

Name: ISO 13408-1:2023 — Aseptic processing of health care products — Part 1: General requirements
SKU: ISO 13408-1:2023
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Aseptic processing of health care products — Part 1: General requirements

Название (английский):

ISO 13408-1:2023

Aseptic processing of health care products — Part 1: General requirements

Статус документа:: Действующий
Формат:: Электронный (PDF)
Количество страниц:: 72
Дата публикации:: 15 августа 2023 г.
Издание:: ISO IS 13408 edition 3 version 1
ICS:: 11.080.01

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Описание (английский):

This document specifies the general requirements for, and offers guidance on, processes, programs and procedures for development, validation and routine control of aseptic processing of health care products. This document includes requirements and guidance relative to the overall topic of aseptic processing. Specific requirements and guidance on various specialized processes and methods related to sterilizing filtration, lyophilization, clean-in place (CIP) technologies, sterilization in place (SIP) and isolator systems are given in the other parts of the ISO 13408 series.

Abstract

Похожие стандарты

Упомянутые в описании и другие стандарты ISO

Overview

ISO 13408-1:2023 - Aseptic processing of health care products - Part 1: General requirements defines the general requirements and guidance for establishing, validating and controlling aseptic processing used in the manufacture of sterile health care products. It covers principles, process design, contamination control, personnel, equipment, environmental monitoring, validation and product release activities that form the foundation of an aseptic processing quality system.

Keywords: ISO 13408-1, aseptic processing, health care products, cleanroom, contamination control, process validation.

Key topics and technical requirements

The standard organizes practical and technical expectations across the aseptic lifecycle. Major topics include:

Principles of aseptic processing

Use of aseptic processes and core elements that support sterility assurance.
Definition of critical processing zone, direct support and indirect support zones for flow and contamination control.

Process design, development and risk management

Risk assessment, identification of critical control points and process parameters.
Materials handling, flow management (containment, item introduction/egress, waste) and process duration considerations.

Contamination Control Strategy (CCS)

Integrated approach including cleaning, disinfection, sterilization and maintenance of sterility.
Cleaning/disinfection program requirements and validation of cleaning/disinfection processes.
Sterilization and depyrogenation considerations; endotoxin control.

Personnel and facility requirements

Roles for training, health monitoring, interventions and cleanroom clothing systems.
Service personnel and maintenance controls.

Equipment, components and single-use systems

Qualification lifecycle (URS, design qualification, IQ/OQ/PQ, requalification) and routine maintenance/calibration.

Environmental monitoring and validation

Non‑viable particulate and microbiological monitoring approaches.
Aseptic process validation (process simulation, initial aseptic qualification, periodic requalification) and documentation.
Product release testing (sterility, bacterial endotoxins, mycoplasma and alternative microbiological methods).

Practical applications - who uses this standard

Pharmaceutical and biotech manufacturers producing sterile injectables, ophthalmics, and parenteral solutions.

Medical device manufacturers of sterile devices and combination products.

Quality assurance/quality control, validation engineers, facility designers, cleanroom managers and regulatory affairs teams.

Contract manufacturing organizations (CMOs) and third‑party sterilization/testing service providers.

ISO 13408-1:2023 PDF

Abstract

Похожие стандарты

Overview

Key topics and technical requirements

Practical applications - who uses this standard

Related standards

Технические детали

BS EN ISO 13408-1:2024

Aseptic processing of health care products. General requirements.

BS EN ISO 13408-3:2011

Aseptic processing of health care products. Lyophilization.

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