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用于非大麻素成分毒理学风险评估的出发点 (POD) 或毒理学关注阈值 (TTC) 的确定（如有必要）的标准指南

Standard Guide for Determining a Point of Departure (POD) or Assigning a Threshold of Toxicological Concern (TTC), if needed, for Use in a Toxicological Risk Assessment of a Non-Cannabinoid Ingredient

用于蒸发用大麻素产品的非大麻素成分的每日吸入暴露限值计算方法的标准实施规程

Standard Practice for Approach to Calculating the Daily Inhalation Exposure Limit for a Non-cannabinoid Ingredient Intended for use in Cannabinoid Products for Vaporization

医疗器械生物学评价第17部分：医疗器械成分毒理学风险评估

Biological evaluation of medical devices - Part 17: Toxicological risk assessment of medical device constituents (ISO/DIS 10993-17:2021); German and English version prEN ISO 10993-17:2021 / Note: Date of issue 2021-11-12*Intended as replacement for DIN...

医疗器械生物学评价 第17部分：医疗器械成分的毒理学风险评估（ISO 10993-17:2023）

Biological evaluation of medical devices - Part 17: Toxicological risk assessment of medical device constituents (ISO 10993-17:2023)

医疗器械的生物学评价-第17部分：医疗器械成分的毒理学风险评估（ISO 10993-17:2023）

Biological evaluation of medical devices - Part 17: Toxicological risk assessment of medical device constituents (ISO 10993-17:2023); German version EN ISO 10993-17:2023

医疗器械生物学评价 第18部分：风险管理过程中医疗器械材料的化学表征

Biological evaluation of medical devices—Part 18: Chemical characterization of medical device materials within a risk management process

医疗器械生物学评价 第17部分：医疗器械成分毒理学风险评估

Biological evaluation of medical devices — Part 17: Toxicological risk assessment of medical device constituents

医疗保健应用中呼吸气体通路的生物相容性评估

Biocompatibility evaluation of breathing gas pathways in healthcare applications

生物医学器械评价 第17部分：医疗器械材料毒理学风险评价（ISO 10993-17:2023）

Biological evaluation of medical devices - Part 17: Toxicological risk assessment of medical device constituents (ISO 10993-17:2023)

无烟草口服尼古丁袋 组成、制造和测试 规格

Tobacco-free oral nicotine pouches. Composition, manufacture and testing. Specification

医疗器械生物学评价 第17部分：医疗器械成分的毒理学风险评估（ISO 10993-17:2023 IDT）

Biological evaluation of medical devices — Part 17: Toxicological risk assessment of medical device constituents (ISO 10993-17:2023, IDT)

医用美利体育官网首页网址的生物评价 第17部分: 医用美利体育官网首页网址成分的毒理风险评估（ISO 10993-17:2023 等同采用）

Biological evaluation of medical devices — Part 17: Toxicological risk assessment of medical device constituents (ISO 10993-17:2023, IDT)

上市药品包装变更等同性/可替代性及相容性研究指南

Guidance of equivalence/replaceability assessment and compatibility studies for postapproval changes to pharmaceutical packages

医疗器械的生物学评价 第17部分：医疗器械成分的毒理学风险评估（ISO 10993-17:2023）

Biological evaluation of medical devices - Part 17: Toxicological risk assessment of medical device constituents (ISO 10993-17:2023)

医疗器械生物学评价 第17部分：医疗器械成分的毒理学风险评估

Biological evaluation of medical devices - Part 17:Toxicological risk assessment of medical device constituents

医疗器械生物学评价 第17部分：医疗器械成分的毒理学风险评估

Biological evaluation of medical devices - Part 17: Toxicological risk assessment of medical device constituents