PD CEN ISO/TS 16791:2020
Health informatics. Requirements for international machine-readable coding of medicinal product package identifiers
Standard number: | PD CEN ISO/TS 16791:2020 |
Pages: | 46 |
Released: | 2020-10-21 |
ISBN: | 978 0 539 00592 9 |
Status: | Standard |
PD CEN ISO/TS 16791:2020 - Health Informatics: Requirements for International Machine-Readable Coding of Medicinal Product Package Identifiers
In the rapidly evolving field of health informatics, the need for standardized, machine-readable coding of medicinal product package identifiers is more crucial than ever. The PD CEN ISO/TS 16791:2020 standard provides comprehensive guidelines and requirements to ensure that medicinal product packages are coded in a way that is universally understandable and accessible by machines across different healthcare systems worldwide.
Overview of the Standard
This standard, officially titled Health Informatics. Requirements for International Machine-Readable Coding of Medicinal Product Package Identifiers, is a pivotal document for professionals in the healthcare and pharmaceutical industries. Released on October 21, 2020, it spans 46 pages of detailed requirements and guidelines. The standard is identified by the number PD CEN ISO/TS 16791:2020 and carries the ISBN 978 0 539 00592 9.
Key Features and Benefits
- International Compatibility: The standard ensures that medicinal product package identifiers are compatible across different countries and healthcare systems, facilitating global trade and communication.
- Machine-Readable Format: By focusing on machine-readable coding, the standard enhances the efficiency of data processing and reduces the risk of human error in the handling of medicinal products.
- Improved Patient Safety: Accurate and standardized coding helps in the prevention of medication errors, thereby improving patient safety and care quality.
- Streamlined Supply Chain Management: The standard aids in the efficient management of the pharmaceutical supply chain, from manufacturing to distribution and retail.
Who Should Use This Standard?
The PD CEN ISO/TS 16791:2020 standard is essential for a wide range of stakeholders in the healthcare and pharmaceutical sectors, including:
- Pharmaceutical Manufacturers: To ensure their products meet international coding requirements.
- Healthcare Providers: To facilitate accurate medication dispensing and administration.
- Regulatory Bodies: To enforce compliance with international standards.
- Software Developers: To create systems that can accurately read and process medicinal product package identifiers.
Why Choose PD CEN ISO/TS 16791:2020?
Adopting the PD CEN ISO/TS 16791:2020 standard offers numerous advantages:
- Global Recognition: As an internationally recognized standard, it ensures that your products and systems are aligned with global best practices.
- Future-Proofing: By adhering to this standard, organizations can stay ahead of regulatory changes and technological advancements.
- Enhanced Efficiency: Streamlined processes and reduced errors lead to cost savings and improved operational efficiency.
Conclusion
In an era where healthcare systems are becoming increasingly interconnected, the PD CEN ISO/TS 16791:2020 standard is a critical tool for ensuring that medicinal product package identifiers are coded in a way that is both machine-readable and internationally compatible. By adopting this standard, organizations can enhance patient safety, improve supply chain management, and ensure compliance with global regulations.
Whether you are a pharmaceutical manufacturer, healthcare provider, regulatory body, or software developer, the PD CEN ISO/TS 16791:2020 standard is an invaluable resource for navigating the complexities of health informatics in the modern world.
PD CEN ISO/TS 16791:2020
This standard PD CEN ISO/TS 16791:2020 Health informatics. Requirements for international machine-readable coding of medicinal product package identifiers is classified in these ICS categories:
- 35.240.80 IT applications in health care technology
This document provides guidelines on identification and labelling of medicinal products from the point of manufacture of packaged medicinal product to the point of dispensing the product.
This document outlines best practice for AIDC barcoding solutions for applications. Users can, however, consider the coding interoperability requirements for other AIDC technologies, e.g. Radio Frequency Identification (RFID).