Circular Economy - Extended Producer Responsibility (EPR) - Requirements and guidelines for Producer Responsibility Organizations (PRO)

Processing of health care products - Information to be provided by the medical device manufacturer for the processing of medical devices - Part 3: Guidance on the designation of a reusable medical device to a quantitative cleaning classification

Water-tube boilers and auxiliary installations - Part 17: Guideline for the involvement of an inspection body independent of the manufacturer

Petroleum and related products - Alternative fuels and fuel blending components assessment guide - Information to producers and blenders of automotive fuels

Circular Economy - Extended Producer Responsibility (EPR) - Requirements and guidelines for Producer Responsibility Organizations (PRO)

Guidelines for end-of-life information provided by manufacturers and recyclers and for recyclability rate calculation of electrical and electronic equipment

Medical devices - Symbols to be used with information to be supplied by the manufacturer - Part 1: General requirements - Amendment 1 (ISO 15223-1:2021/DAM 1:2024); German and English version EN ISO 15223-1:2021/prA1:2024

Medical devices - Information to be supplied by the manufacturer (ISO/DIS 20417:2024); German and English version prEN ISO 20417:2024

Measurement of radioactivity in the environment - Air: Radon-222 - Quality assurance and quality control for calibration facilities, radon measurement device manufacturers and measurement device analysis providers

Medical devices - Symbols to be used with information to be supplied by the manufacturer - Part 1: General requirements - Amendment 1: Addition of defined term for authorized representative and Modified EC REP symbol to not be country or region specific (ISO 15223 1:2021/DAM 1:2024)