BS EN ISO 17523:2025 - Health Informatics: Requirements for Electronic Prescriptions

In the rapidly evolving world of healthcare, the need for efficient, secure, and standardized electronic prescriptions is more critical than ever. The BS EN ISO 17523:2025 standard is a comprehensive guide that sets forth the requirements for electronic prescriptions, ensuring that healthcare providers can deliver prescriptions in a manner that is both safe and effective.

Overview of the Standard

The BS EN ISO 17523:2025 is a pivotal document in the field of health informatics, focusing on the requirements for electronic prescriptions. Released on August 7, 2025, this standard is designed to enhance the interoperability and security of electronic prescription systems across various healthcare settings.

Key Features

• Standard Number: BS EN ISO 17523:2025
• Pages: 34
• ISBN: 978 0 539 25744 1
• Status: Standard

Why This Standard Matters

Electronic prescriptions are a cornerstone of modern healthcare, offering numerous benefits over traditional paper prescriptions. They reduce errors, enhance patient safety, and streamline the prescription process. However, without a standardized approach, the potential for miscommunication and data breaches increases. The BS EN ISO 17523:2025 addresses these challenges by providing a robust framework for the secure and efficient exchange of electronic prescriptions.

Benefits of Implementing BS EN ISO 17523:2025

• Improved Patient Safety: By minimizing prescription errors and ensuring accurate data exchange, this standard enhances patient safety.
• Enhanced Interoperability: Facilitates seamless communication between different healthcare systems, ensuring that prescriptions are accurately transmitted and received.
• Data Security: Establishes stringent security protocols to protect sensitive patient information from unauthorized access.
• Efficiency: Streamlines the prescription process, reducing the time and resources required to manage prescriptions.

Who Should Use This Standard?

The BS EN ISO 17523:2025 is essential for a wide range of stakeholders in the healthcare industry, including:

• Healthcare Providers: Doctors, nurses, and pharmacists who are involved in prescribing and dispensing medications.
• Healthcare IT Professionals: Individuals responsible for implementing and maintaining electronic health record systems.
• Policy Makers: Government and regulatory bodies involved in setting healthcare standards and regulations.
• Software Developers: Companies and individuals developing electronic prescription software and systems.

Conclusion

The BS EN ISO 17523:2025 is a vital resource for anyone involved in the healthcare industry. By adhering to this standard, organizations can ensure that their electronic prescription systems are secure, efficient, and interoperable. This not only enhances patient care but also contributes to the overall improvement of healthcare delivery systems.

With its comprehensive guidelines and focus on security and interoperability, the BS EN ISO 17523:2025 is an indispensable tool for modern healthcare providers looking to optimize their electronic prescription processes.

BS EN ISO 17523:2025

This standard BS EN ISO 17523:2025 Health informatics. Requirements for electronic prescriptions is classified in these ICS categories:

• 35.240.80 IT applications in health care technology

The scope of this document is constrained to the content of the electronic prescription (ePrescription) itself, the digital document which is issued by a prescribing healthcare professional and received by a dispensing healthcare professional. The prescribed medicinal product is to be dispensed through an authorized healthcare professional with the aim of being administered to a human patient. The ePrescription in the administrative workflow of reimbursement is not covered in this document. This document specifies the requirements that apply to ePrescriptions. It describes generic principles that are considered important for all ePrescriptions. This document is applicable to ePrescriptions of medicinal products for human use. Although other kinds of products (e.g. medical devices, wound care products) can be ordered by means of an ePrescription, the requirements in this document are aimed at medicinal products that have a market authorization and at pharmaceutical preparations which are compounded in a pharmacy. This document does not limit the scope to any setting (community, institutional) and leaves it to the national bodies to decide on this matter. This document specifies a list of data elements that can be considered as essential for ePrescriptions, depending on jurisdiction or clinical setting (primary healthcare, hospital, etc.). Ensuring the authenticity of these data elements is in scope and will have impact on the requirements of information systems. Other messages, roles and scenarios (e.g. validation of a prescription, administration, medication charts, EHR of the patient, reimbursement of care and dispensed products) are not covered in this document, because they are country-specific or region-specific, due to differences in culture and in legislation of healthcare. However, requirements and content of ePrescriptions within the context of jurisdictions have a relationship with these scenarios. This document also does not cover the way in which ePrescriptions are made available or exchanged, and the process of prescribing itself. The logistic process of prescribing itself is not part of the scope. A prescription can either be sent (pushed) to a dispenser or either be retrieved (pulled) at the dispenser. However, the requirement for the prescription is described, that it will be able to function in both environments.