Department of Crop Genetics, John Innes Centre, Norwich, UK.
Mol Biotechnol. 2010 Mar;44(3):267-75. doi: 10.1007/s12033-009-9237-x.
GM risk assessments (GMRAs) play an important role in the decision-making process surrounding the regulation, notification and permission to handle Genetically Modified Organisms (GMOs). Ultimately the role of each GMRA will be able to ensure the safe handling and containment of the GMO; and to asses any potential impacts on the environment and human health. A risk assessment should answer all "what if" scenarios, based on scientific evidence. This article sets out to provide researchers with helpful guidance notes on producing their own GMRA. While reference is made to UK and EU regulations, the underlying principles and points to consider are generic to most countries.
遗传修饰生物体(GMO)的风险评估(GMRA)在管理、通知和处理 GMO 的监管决策过程中发挥着重要作用。最终,每个 GMRA 的作用都将能够确保 GMO 的安全处理和控制;并评估对环境和人类健康的任何潜在影响。风险评估应根据科学证据回答所有“如果......会怎样”的情况。本文旨在为研究人员提供关于编写自己的 GMRA 的有用指导说明。虽然提到了英国和欧盟的法规,但基本原则和需要考虑的要点对大多数国家都是通用的。