Abstract

This paper gives an overview of scientific challenges in implementing and certifying “Zero residue” approach. The rationale behind the concept is that final control of commodities during/immediately after harvesting should confirm that traces of all used plant protection products are less than or equal to 0.01 mg/kg. To evaluate the risks in applying this concept, FMEA (Failure Mode and Effect Analysis) as a tool has been used. Among the most common factors affecting the pesticide residue levels in fresh produce, the following three appeared to be the biggest challenges in the “Zero residue” concept implementation and certification process: the use of unregistered plant protection products, inadequate sampling plan, and inappropriate laboratory methods. The analysis showed that all three factors have strong influence on achieving “Zero residue” limits.

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