Question

"In accordance with the FDA's 1986 policy under CFRB, FDA intends to regulate foods produced by rDNA techniques, within the existing regulatory framework that applies for foods produced by traditional breeding techniques. What does CFRB stand for?"

-Common Framework for the Regulation of Bioproducts
-Center for the Regulation of Biotechnology
-Coordinated Framework for the Regulation of Biotechnology
-Committee For Regulation of Biotechnology
-Consolidated Framework for the Release of Biotechnology

Answer 1

CFRB stands for the Coordinated Framework for the Regulation of Biotechnology, which regulates foods produced by rDNA techniques. This framework ensures the safety of biotechnology products, including those in the medical and agricultural sectors.

Step-by-step explanation:

The acronym CFRB refers to the Coordinated Framework for the Regulation of Biotechnology. Established in 1986, the policy was designed to provide a comprehensive regulatory framework for the oversight of foods produced by recombinant DNA (rDNA) techniques and ensures that they meet the same safety standards as foods developed through traditional breeding techniques. The Center for Biologics Evaluation and Research (CBER) is a branch of the FDA responsible for the safety and effectiveness of biological therapeutic agents like vaccines, blood and tissue products, and products derived from biotechnology.

Recombinant DNA technology has significant applications in medicine, such as the production of human insulin and different vaccines. This technology is also used in agriculture to produce genetically modified crops with enhanced qualities. Under CBER's guidance, such products are subject to careful regulation to ensure they are safe for consumption and use.