Biological evaluation of medical devices. Guidance on the conduct of biological evaluation within a risk management process
Edition 2017-01-31

IEEE Standard for Access and Control of Instrumentation Embedded within a Semiconductor Device
Edition 2014

Guidance for the Application of AQAP 2110 within a 9100 Quality Management System
Edition 2024-02-16

Biological evaluation of medical devices Part 1: Evaluation and testing within a risk management process
Edition 2022-05-12

BS EN ISO 10993-1 Biological evaluation of medical devices. Part 1. Evaluation and testing within a risk management process
Edition 2024-06-24

Industrial systems, installations and equipment and industrial products - Identification of terminals within a system (Endorsed by Asociación Española de Normalización in September of 2021.)
Edition 2021-09-01

Industrial systems, installations and equipment and industrial products - Identification of terminals within a system (Endorsed by AENOR in May of 2011.)
Edition 2011-05-01

Biological evaluation of medical devices - Part 18: Chemical characterization of medical device materials within a risk management process (ISO 10993-18:2020)
Edition 2021-01-20

Electronic cigarettes and e-liquids - Determination of nicotine delivery consistency over defined puff sequences within a single e-cigarette
Edition 2024-01-17

BS EN ISO 18562-1. Biocompatibility evaluation of breathing gas pathways in healthcare applications. Part 1. Evaluation and testing within a risk management process
Edition 2022-12-02