FAQs
SS ISO 15223-1:2021
Medical devices – Symbols to be used with information to be supplied by the manufacturer – Part 1 : General requirements
SS ISO 35001:2021
Biorisk management for laboratories and other related organisations
SS IEC 60601-1-11 (+A1):2018
Medical electrical equipment – Part 1-11 : General requirements for basic safety and essential performance – Collateral standard: Requirements for medical electrical equipment and medical electrical systems used in
SS ISO 14065:2021
General principles and requirements for bodies validating and verifying environmental information
SS IEC 62366-1 (+A1):2018
Medical devices – Part 1 : Application of usability engineering to medical devices
SS ISO 50004:2021
Energy management systems – Guidance for the implementation, maintenance and improvement of an ISO 50001 energy management system
SS ISO 14155:2020
Clinical investigation of medical devices for human subjects — Good clinical practice
SS ISO 10993-12:2021
Biological evaluation of medical devices – Part 12 : Sample preparation and reference materials
SS ISO 14064-3:2021
Greenhouse gases – Part 3 : Specification with guidance for the verification and validation of greenhouse gas statements