Popular ISO 9001 Quality management > ISO 13485 Quality Management for Medical Devices > ISO 14001 Environmental management > ISO 22301 Business continuity > ISO/IEC 27001 Information security > ISO 45001 (OHSAS 18001) Occupational health and safety > View all standards >
Access and buy standards How to access and buy > Decide which option works best for your business Buy standards > BSOL > Full standards collections Compliance Navigator > Medical device standards
Auditing, certification and training Assessment and ISO certification > ISO certification and others eg: IATF, FSSC Auditing and verification > Supplier audits, custom audits and internal audits Product testing and certification > BSI Kitemark, CE marking and verification, Market access solutions Validate BSI-issued certificates > Check company, site and product certificates
Training courses > Individual, group and company-wide training Medical devices services > CE marking for medical devices, MDR and IVDR, quality management for medical devices
Industry reports, research and news Digital construction > BIM, smart cities and connected assets Future of mobility > Global market access > Health, safety and wellbeing > Information security > Cybersecurity, privacy (GDPR) and compliance
About BSI > BSI impartiality > Our accreditation > Our clients and partners > Our financial information >
Our governance > Our legal information > Our purpose, mission and vision > Our Royal Charter > UK National Standards body > The global role of BSI as the national standards body >
Careers > Events and webinars > Media centre/press room > Sustainability > Modern slavery statement Contact us >
CE Marking: European Regulations > ISO 13485 Quality Management Systems > Medical Device Single Audit Program (MDSAP) > ISO 14971 Risk Management > EN 60601 Electro-medical Electrical > Compliance Navigator > Training Courses >
Popular topics BSI Medical Devices and Brexit > OBL / Virtual Manufacturers > Transfer to BSI > Unannounced Audits > Role of the Notified Body > Product Lifecycle >
Featured training ISO 13485 Transition & Auditor Refresher > ISO 13485 Senior Management Briefing > Medical Device Single Audit Program (MDSAP) >
AIMD > Active Devices > Ancillary medicinal substances > In Vitro Diagnostics > Devices utilizing animal tissue > Electronic Cigarettes > Microbiology and Sterile Devices > View all technologies >
Mobile Devices > Ophthalmic Devices > Orthopaedic and Dental Devices > Software as a Medical Device > Vascular Devices > Woundcare > DuPont™ Tyvek® Transition Project >
Webinars > White papers > Training courses > Brochures > Newsletters > Events > Industry guidance > Case studies >
Book now for the BSI IVDR Spring Roadshow BSI’s In Vitro Diagnostics Regulation (IVDR) Roadshow will be returning in Spring 2020 in various locations in Europe. Come along to hear the latest IVDR updates from BSI and engage face-to-face with the only organization with two Notified Bodies with full scope designation to the IVDR. European locations - book your seat today >
BSI product experts speaking at events As one of the world’s leading organizations dedicated to raising standards, our product experts speak at industry conferences and events across the world. View a list of where our product experts are speaking >
Webinars We offer a wide range of free webinars addressing key topics that affect your business. Visit our webinars page to find out more. View all webinars >
