BS EN 16777:2018

Comprehensive Healthcare Technology Standard

BS EN 16777:2018 is the essential standard for healthcare providers, medical device manufacturers, and service providers. This European Standard specifies requirements and recommendations for the design, development, and implementation of healthcare technology solutions.

Ensure Compliance and Best Practices

Compliance with BS EN 16777:2018 is crucial for organizations operating in the healthcare sector. The standard outlines best practices and technical specifications to:- Enhance patient safety and care quality- Improve operational efficiency and cost-effectiveness- Mitigate risks and ensure regulatory compliance

Detailed Technical Specifications

This 40-page standard covers a wide range of technical requirements and guidelines, including:• General system design principles• Hardware and software requirements• Cybersecurity and data protection measures• Maintenance, servicing, and lifecycle management• Usability and human factors engineering• Validation and verification procedures

Key Benefits of BS EN 16777:2018

• Enhances patient outcomes and care quality• Improves operational efficiency and cost-savings• Ensures compliance with relevant regulations and standards• Mitigates risks and liabilities associated with healthcare technology• Promotes best practices in the design, development, and implementation of medical devices and services

Who Should Use This Standard?

BS EN 16777:2018 is an essential resource for a wide range of healthcare stakeholders, including:• Healthcare providers (hospitals, clinics, long-term care facilities)• Medical device and technology manufacturers• Healthcare IT and service providers• Regulatory bodies and policymakers• Healthcare professionals and researchersImplementing the requirements and recommendations of BS EN 16777:2018 can help organizations in the healthcare sector deliver safer, more effective, and more efficient technology-enabled services.