BS ISO 21882:2019 - Sterile Packaged Ready for Filling Glass Vials

Introducing the BS ISO 21882:2019, a comprehensive standard that sets the benchmark for sterile packaged ready for filling glass vials. This essential document is a must-have for professionals in the pharmaceutical and medical industries, ensuring the highest standards of quality and safety in the packaging and handling of glass vials.

Overview

The BS ISO 21882:2019 standard provides detailed guidelines and specifications for the production and packaging of sterile glass vials that are ready for filling. Released on October 23, 2019, this standard is a critical resource for manufacturers and quality assurance teams who are committed to maintaining the integrity and sterility of their products.

Key Features

• Standard Number: BS ISO 21882:2019
• Pages: 28
• ISBN: 978 0 580 95918 9
• Status: Standard

Why Choose BS ISO 21882:2019?

In the highly regulated field of pharmaceuticals, maintaining sterility and quality is paramount. The BS ISO 21882:2019 standard is designed to help you achieve these goals by providing a clear framework for the production and packaging of glass vials. Here are some reasons why this standard is indispensable:

Ensures Sterility

One of the primary concerns in the pharmaceutical industry is the sterility of packaging materials. This standard outlines the necessary steps and precautions to ensure that glass vials remain sterile from production to filling, minimizing the risk of contamination.

Quality Assurance

With detailed specifications and guidelines, the BS ISO 21882:2019 standard helps manufacturers maintain consistent quality in their products. This consistency is crucial for building trust with clients and regulatory bodies.

Compliance with International Standards

Adhering to the BS ISO 21882:2019 standard ensures that your products meet international quality and safety requirements. This compliance is essential for companies looking to expand their market reach and operate globally.

Comprehensive Guidelines

Spanning 28 pages, this standard provides a thorough overview of the requirements for sterile packaged glass vials. It covers everything from material selection and manufacturing processes to packaging and labeling, offering a complete guide for industry professionals.

Who Should Use This Standard?

The BS ISO 21882:2019 standard is ideal for a wide range of professionals and organizations, including:

• Pharmaceutical manufacturers
• Quality assurance teams
• Regulatory compliance officers
• Packaging engineers
• Research and development teams

Conclusion

In an industry where precision and safety are non-negotiable, the BS ISO 21882:2019 standard is an invaluable resource. By following its guidelines, you can ensure that your glass vials are produced and packaged to the highest standards of sterility and quality. Whether you are a manufacturer, quality assurance professional, or regulatory officer, this standard will help you achieve excellence in your operations.

Invest in the BS ISO 21882:2019 standard today and take a significant step towards ensuring the safety and reliability of your pharmaceutical products.

BS ISO 21882:2019

This standard BS ISO 21882:2019 Sterile packaged ready for filling glass vials is classified in these ICS categories:

• 11.080.30 Sterilized packaging

This document specifies the characteristics of sterile and ready for filling empty glass vials for injectable preparations, including the minimum requirements of materials, packaging systems and analytical test methods.