汇总 HESI 研讨会:发育和生殖毒性终点的解释以及不良事件对数据解释的影响
M L Green1, A Kluever2, Connie Chen3
1Hurley Consulting Associates, Ltd., Summit, New Jersey, USA.
Birth defects research
|February 12, 2024
概括
卫生和环境科学研究所发育和生殖毒理学 (HESI-DART) 研讨会确立了评估化学风险的共识原则. 这些原则指导监管决策的危险识别和风险评估.
科学领域:
- 毒理学 毒理学 毒理学
- 风险评估 风险评估
- 监管科学 监管科学
背景情况:
- 卫生和环境科学研究所发育和生殖毒理学 (HESI-DART) 组召开了2022年关于在监管环境中解释DART发现的研讨会.
- 评估DART风险至关重要,因为对动物试验,标签和临床试验的下游影响.
研究的目的:
- 在发生非临床发现时,建立共识方法来评估化学物质暴露的DART风险.
- 在化学和制药行业的监管框架中协调数据解释原则.
主要方法:
- 一个混合研讨会,涉及来自不同科学背景的154名国际参与者.
- 网络研讨会模块集中在解释DART数据的最佳实践和监管框架内的新方法方法论上.
主要成果:
- 为系统的数据解释制定两步原则分类.
- 步骤1:通过详细的研究终点分析识别危险.
- 步骤2:使用权重证据方法进行风险评估.
结论:
- 研讨会提供了在监管环境中对DART数据的一致解释的指导原则.
- 这些原则旨在提高化学产品风险评估的准确性和效率.
- 协调解释支持知情的监管决策,并减少潜在的负面影响.
更多相关视频
17:28Human Pluripotent Stem Cell Based Developmental Toxicity Assays for Chemical Safety Screening and Systems Biology Data Generation
Published on: June 17, 2015
12.6K
16:02Demonstration of the Sequence Alignment to Predict Across Species Susceptibility Tool for Rapid Assessment of Protein Conservation
Published on: February 10, 2023
2.7K
相关概念视频
Teratogenicity
2.4K
The ability of a drug to produce structural deformations and functional abnormalities in the developing embryo or the fetus is called teratogenicity, and the drug producing this effect is known as a teratogen. Teratogenic effects include stillbirth, miscarriage, intrauterine growth restriction, and neurocognitive delay. A teratogen may affect the embryo at different stages of development, which is important in determining the type and extent of the damage. During blastocyst formation, the early...
2.4K
Mutagenicity and Carcinogenicity
1.3K
Mutagenicity and carcinogenicity refer to the ability of drugs to cause genetic defects and induce cancer, respectively. The International Agency for Research on Cancer (IARC) classifies agents into four groups based on their carcinogenic potential. Group 1 agents are known human carcinogens; group 2A agents are probably carcinogenic to humans; group 3 agents lack data to support their role in carcinogenesis; and group 4 includes agents for which data support that they are not likely to be...
1.3K
Types of Biopharmaceutical Studies: Controlled and Non-Controlled Approaches
126
Biopharmaceutical studies constitute a vital field aiming to enhance drug delivery methods and refine therapeutic approaches, drawing upon diverse interdisciplinary knowledge. In research methodologies, the choice between controlled and non-controlled studies significantly influences the study's reliability and accuracy.
Non-controlled studies, commonly employed for initial exploration, lack a control group, rendering them susceptible to biases and external influences. In contrast,...
Non-controlled studies, commonly employed for initial exploration, lack a control group, rendering them susceptible to biases and external influences. In contrast,...
126
