Monday, May 29, 2017 by Russel Davis
The U.S. Food and Drug Administration (FDA) has extended its Request for Comment period on genome edited foods and animals. The move aims to continue gaining public input on the draft revised guidance about the agency’s stance on human and animal foods derived from plants that have undergone genome editing. The federal agency has also extended the comment period for the draft guidance regarding the regulation of intentionally-engineered genomic DNA in animals. The FDA’s recent action was in response to requests for additional time to submit comments. The comment periods for the two draft guidance will close on June 19, 2017.
The two draft guidance were originally released in January, which discuss the steps that the federal agency takes to clarify how it regulates specific biotechnology products. The recent announcements were in line with the federal agency’s commitments highlighted in the “National Strategy for Modernizing the Regulatory System for Biotechnology Products” issued in September last year. The document aims to ensure that the FDA is efficiently equipped to evaluate any risks associated with future biotechnology products.
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In its blog the FDA Voice, the federal agency outlined that recent scientific innovations have led to the development of more efficient and precise methods in modifying plant, animal, and microorganism genomes to produce ideal traits. According to the FDA, these genome editing technologies were relatively easy to use, and may have extensive applications to a wide range of sectors including the medical, food and environmental industries. The federal agency also noted that genome-editing technologies may have potential use in the introduction, removal, or replacement of one or more specific nucleotides at a specific region in the organism’s genome. According to the agency, a number of research are currently at work to determine how genome-editing technologies can be applied to the following:
However, the federal agency also stressed on the potential risks associated with genome editing technologies. According to the FDA, the risks include the technology’s effects on individual genomes, and its potential impact on the environment and ecosystem.