Standards Worldwide
Standards Worldwide
Phone +49 30 58885700-07

Standard [CURRENT]

ASTM E 3051:2025

Standard Guide for Specification, Design, Verification, and Application of Single-Use Systems in Pharmaceutical and Biopharmaceutical Manufacturing

Publication date
2025
Original language
English
Pages
11

from 81.30 EUR VAT included

from 75.98 EUR VAT excluded

Format and language options

PDF download
  • 81.30 EUR

  • 97.60 EUR

Shipment (3-5 working days)
  • 90.40 EUR

Monitor with the Standards Ticker

This option is only available after login.
Easily subscribe: Save time and money now!

You can also subscribe to this document - together with other important standards in your industry. This makes your work easier and pays for itself after a short time.

Sparschwein_data
Subscription advantages
Sparschwein Vorteil 1_data

Important standards for your industry, regularly updated

Sparschwein Vorteil 2_data

Much cheaper than buying individually

Sparschwein Vorteil 3_data

Useful functions: Filters, version comparison and more

Publication date
2025
Original language
English
Pages
11
DOI
https://dx.doi.org/10.1520/E3051-25

Quick delivery via download or delivery service

Buy securely with a credit card or pay upon receipt of invoice

All transactions are encrypted

Short description
1.1 This guide is intended as a complement to Guide E2500 . 1.2 This guide is applicable to the range of manufacturing systems described in Guide E2500 , specifically all elements of single-use systems, or hybrids of single-use and traditional components, used for the manufacturing of pharmaceutical and biopharmaceutical products, including: materials of construction, components, assembly, manifolds, supporting utilities, associated process monitoring and control systems, automation systems, and controlled environment that have the potential to affect product quality and patient safety. 1.3 This guide is applicable for the implementation of changes to manufacturing system design for existing systems. It may be used for continuous improvement and changes in operation from clinical through to commercial scale. 1.4 For brevity, single-use systems are referred to as SUS throughout the rest of this guide. 1.5 The approach may be applied by the end user, the supplier of SUS, and raw materials sub-suppliers further back in the supply chain. 1.6 This guide is not intended to apply to the use of single-use technology for packaging, primary containers, combination products (products composed of any combination of a drug, device, or biological product) or devices. 1.7 This guide does not address specific local requirements, which remain the responsibility of the end user. 1.8 This guide does not address employee health and safety, environmental, nor other good engineering and manufacturing practices (GxP) requirements. This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety, health, and environmental practices and determine the applicability of regulatory limitations prior to use. 1.9 This international standard was developed in accordance with internationally recognized principles on standardization established in the Decision on Principles for the Development of International Standards, Guides and Recommendations issued by the World Trade Organization Technical Barriers to Trade (TBT) Committee.
ICS
11.120.99
DOI
https://dx.doi.org/10.1520/E3051-25
Also available in
Loading recommended items...
Loading recommended items...
Loading recommended items...
Loading recommended items...