Press "Enter" to skip to content

Insights on Necessary Changes in Gene Edited Animals

Since the last couple of years, the Food and Drug Administration and the United States Department of Agriculture has struggled to reach an agreement regarding which one of the two agencies should take over the regulatory standards of gene-edited Animals. Newly emerging recommendations are now appealing for updating the pre-existing FDA regulatory framework, followed by developing a coordinated and streamlined procedure for assessment and approval among the FDA and USDA.

For the last eighteen months, a panel consisting of experts from the American Association of Veterinary Medical Colleges (AAVMC) and the Association of Public and Land-grant Universities (APLU) evaluated data for enabling gene editing in agriculture Animals.Gene editing in agriculture holds immense potential to generate massive gains in terms of productivity. There is a crucial requirement for remodeling the federal regulatory structure.

The AAVMC/APLU published Gene Editing in Agriculture Taskforce Report indicates that the present-day protocols cannot cope with the advancing technologies and are in desperate need of modernization to impart accurate understanding to society associated with the novel scientific capabilities.Public perception of GMO-derived agricultural or Animals products has inclined on the negative side, and there is still a dominating preference for opting for non-GMO products.

In the current scenario, the most significant application of the technology associated with genetic engineering has transformed gene editing.At present, the Food and Drug Administration regulates genetic work done on food Animals in the name of the Animals drug under strict protocols established in the maiden days of the Biotechnology Revolution.

Be First to Comment

Leave a Reply

Your email address will not be published. Required fields are marked *