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Microbiology Audit

The purpose of this document is to provide guidance to prepare for Microbiology Audits.

Brochures

Medical Device Expertise and Technologies from BSI

BSI is a leading global organization with technical expertise and experience from a notified body for medical device technologies and...

Medical Devices focus

UKCA Certification Transfer to BSI

Transfer your UKCA certification to BSI with confidence. Understand the UKCA transfer process, requirements, and key steps for medical devices.

Brochures

Facility Management (ISO 41001)

Driving consistency and value across your facilities.

System Certification

A Circular Energy Revolution - Circularity in the Renewable Energy Sector

Learn how the renewable energy sector can adopt a circular economy to accelerate progress to a sustainable world.

Blogs

PAS 2009:2024 Digital Maturity for Organizations Guide

PAS 2009 gives guidance to government organizations on how to increase their digital maturity. It covers operations, service delivery and...

Brochures

MDR Documentation Submission

Get comprehensive guidance on documentation submission requirements under the Medical Device Regulation (MDR) with BSI's informative brochure.

Brochures

Umony achieves ISO/IEC 42001 certification for responsible AI

Umony evidences responsible AI via an independently certified AIMS, strengthening client assurance and supporting alignment with evolving regulations.

Case Studies

Clinical Evaluation for Medical Software & AI Devices

Gain insights into clinical evaluation requirements for medical software and AI devices under MDR.

Webinars

Kurs eLearningowy: Szkolenie wprowadzające dotyczące diagnostyki In Vitro

Z kursu dowiesz się jak IVDR nadaje priorytet bezpieczeństwu, skuteczności i najwyższym standardom zdrowia publicznego w UE.

Training & Qualifications