Jove
Visualize
联系我们
JoVE
x logofacebook logolinkedin logoyoutube logo
关于 JoVE
概览领导团队博客JoVE 帮助中心
作者
出版流程编辑委员会范围与政策同行评审常见问题投稿
图书馆员
用户评价订阅访问资源图书馆顾问委员会常见问题
研究
JoVE JournalMethods CollectionsJoVE Encyclopedia of Experiments存档
教育
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab Manual教师资源中心教师网站
使用条款与条件
隐私政策
政策

相关概念视频

Drug Regulation01:25

Drug Regulation

1.3K
Drug regulation encompasses the management of drug usage by evaluating its safety and efficacy through assessments conducted by regulatory authorities. Regrettably, the history of drug regulation is marred by several catastrophic events. One such incident is the Elixir Sulfanilamide tragedy, in which the toxic compound diethyl glycol was included in a sweet-tasting medication, leading to numerous fatalities. This event prompted the enactment of the Food, Drug, and Cosmetic Act in 1938. Under...
1.3K
Data Validation01:15

Data Validation

153
Method validation is a crucial process in analytical chemistry designed to confirm that a given method consistently produces reliable and high-quality results. This process is essential when a method is applied to different sample matrices or when procedural modifications are made, ensuring that the results meet acceptable standards across various applications.
Key parameters for method validation include:
153
Effects of Chemicals: Overview01:27

Effects of Chemicals: Overview

1.2K
Drugs, encompassing various chemical compounds from natural sources, lab synthesis, or genetic engineering, elicit different biological responses in living organisms. Some of these responses are desirable or therapeutic, while others are undesirable. The primary goal of administering a drug is to achieve a therapeutic effect, that is, to address a specific disease or health condition. Any concurrent effects outside of this therapeutic outcome are considered undesirable. These undesirable...
1.2K
Drug Classes and Categories01:25

Drug Classes and Categories

1.9K
Drugs can be classified according to their chemical composition or their intended therapeutic application. For instance, anti-infective agents that possess the ability to eliminate pathogens or suppress their growth and reproduction can be grouped based on the organisms they target or their chemical structure. Furthermore, drugs can be divided into prescription, nonprescription, or controlled substances. Prescription medications, such as antibiotics, require oversight from a licensed healthcare...
1.9K
Measurement: Derived Units03:02

Measurement: Derived Units

42.9K
The International System of Units or SI system, by international agreement, has fixed measurement units for seven fundamental properties: length, mass, time, temperature, electric current, amount of substance, and luminosity. These are called the SI base units.
42.9K

您也可能阅读

相关文章

通过共同作者、期刊和引用图与本文相关的文章。

排序
Same author

Aligning Horizon Scanning Approaches with Differing Needs and Topics at the Science-Policy Interface on Chemicals, Waste, and Pollution.

Environmental science & technology·2026
Same author

60 Years of Science on Contaminants of Emerging Concern in <i>ES&T</i>: From Serendipitous Discoveries to a More Systematic Understanding.

Environmental science & technology·2026
Same author

PFASGroups: An Open-Source Framework for Automated Identification, Structural Classification, and Prioritization of Per- and Polyfluoroalkyl Substances.

Journal of chemical information and modeling·2026
Same author

Planetary Boundary for Novel Entities: Time for a Reboot.

Environmental science & technology·2026
Same author

Legacy and Emerging Per- and Polyfluoroalkyl Substances (PFAS) in Glacial Meltwater from Mt. Everest.

Environmental science & technology·2026
Same author

Response to Letter to the Editor Regarding "Is Persistence a Hazard?"

Environmental science & technology·2026

相关实验视频

Updated: Jun 16, 2025

Identifying Per- and Polyfluorinated Chemical Species with a Combined Targeted and Non-Targeted-Screening High-Resolution Mass Spectrometry Workflow
09:04

Identifying Per- and Polyfluorinated Chemical Species with a Combined Targeted and Non-Targeted-Screening High-Resolution Mass Spectrometry Workflow

Published on: April 18, 2019

12.4K

在化学品立法中实施"基本用途"概念的数据要求.

Romain Figuière1, Zhanyun Wang2, Juliane Glüge3

  • 1Department of Environmental Science, Stockholm University, SE-10691 Stockholm, Sweden.

Environmental science & technology
|June 2, 2025
PubMed
概括

基本用途概念可以指导化学品法规,如斯德哥尔摩公约和欧盟REACH. 这项研究表明,现有法规已经包含了基本性,不需要对数据进行重大修改才能实施.

关键词:
基本使用概念的概念.微塑料是一种微塑料.REACH 授权程序 授权过程在REACH法规中,规定了REACH法规.对化学品进行合理管理.斯德哥尔摩公约 斯德哥尔摩公约

更多相关视频

In Silico Modeling Method for Computational Aquatic Toxicology of Endocrine Disruptors: A Software-Based Approach Using QSAR Toolbox
00:05

In Silico Modeling Method for Computational Aquatic Toxicology of Endocrine Disruptors: A Software-Based Approach Using QSAR Toolbox

Published on: August 28, 2019

13.9K
High Content Screening Analysis to Evaluate the Toxicological Effects of Harmful and Potentially Harmful Constituents HPHC
11:38

High Content Screening Analysis to Evaluate the Toxicological Effects of Harmful and Potentially Harmful Constituents HPHC

Published on: May 10, 2016

12.2K

相关实验视频

Last Updated: Jun 16, 2025

Identifying Per- and Polyfluorinated Chemical Species with a Combined Targeted and Non-Targeted-Screening High-Resolution Mass Spectrometry Workflow
09:04

Identifying Per- and Polyfluorinated Chemical Species with a Combined Targeted and Non-Targeted-Screening High-Resolution Mass Spectrometry Workflow

Published on: April 18, 2019

12.4K
In Silico Modeling Method for Computational Aquatic Toxicology of Endocrine Disruptors: A Software-Based Approach Using QSAR Toolbox
00:05

In Silico Modeling Method for Computational Aquatic Toxicology of Endocrine Disruptors: A Software-Based Approach Using QSAR Toolbox

Published on: August 28, 2019

13.9K
High Content Screening Analysis to Evaluate the Toxicological Effects of Harmful and Potentially Harmful Constituents HPHC
11:38

High Content Screening Analysis to Evaluate the Toxicological Effects of Harmful and Potentially Harmful Constituents HPHC

Published on: May 10, 2016

12.2K

科学领域:

  • 环境法 环境法 环境法
  • 化学品法规 化学品法规
  • 风险评估 风险评估

背景情况:

  • 斯德哥尔摩公约和欧盟REACH法规是关键的全球和欧洲化学品立法.
  • 关于修订的讨论正在进行中,包括逐步淘汰有害化学品的"必要用途"概念.

研究的目的:

  • 评估基本用途概念如何为化学品法规中的豁免做出决定提供信息.
  • 提供有关实施基本使用概念的见解.
  • 通过微塑料案例研究,探索使用现有的数据要求进行基本性评估.

主要方法:

  • 根据"斯德哥尔摩公约"对34起案件的分析.
  • 根据REACH (截至2023年11月) 审查了45项限制和544份授权申请.
  • 关于REACH限制故意添加的微塑料的详细案例研究.

主要成果:

  • 基本用途概念的要素已经存在于斯德哥尔摩公约和REACH的决策过程中.
  • 监管框架内现有的数据要求适用于基本性评估.
  • 为了实现基本用途概念,不需要对数据要求进行重大修改.

结论:

  • 斯德哥尔摩公约和REACH法规可以在没有实质性修改的情况下有效地整合基本用途概念.
  • 该研究为在化学品管理中应用基本用途概念提供了一个框架.
  • 这些发现支持继续使用和完善现有的化学安全监管工具.