On November 14, 2011, APHIS announced plans to streamline and improve the agency's process for making determinations on petitions for nonregulated status for genetically engineered (GE) organisms. APHIS reviews such petitions in order to determine whether a GE organism poses a plant pest risk and, if not, should no longer be subject to APHIS regulation under 7 CFR part 340.
Since the petition process was first added to APHIS biotechnology regulations in 1992, the time it takes the Agency to reach a final decision has grown from six months on average to three to five years or more. As a result of these improvements, APHIS expects to reduce the length of the petition review by half, while also reducing the variability of the timeframe from one petition to another.
APHIS used Lean Six Sigma (LSS) business process improvement techniques to identify and address the root causes of the length and variability of the process, and to develop improvements to address those underlying root causes.
The new enhancements include:
By taking these steps, APHIS believes it can deliver to its customers and the public a more predictable process for considering and acting on petitions, without compromising the quality of the analysis supporting our decisionmaking.
Learn More about enhancements to the way APHIS solicits public input on petitions
Learn more about transition of pending petitions into the improved process
Last Modified: March 5, 2012