My company is a 3PL that primarily stores frozen/refrigerated goods...both finished goods and raw ingredients. We also have a couple of pharmaceutical customers. We are looking to go SQF within the next year. My question is, is there anything in the SQF scheme that would prohibit or hinder certification due to storing pharmaceutical product? Some of the product is raw ingredient to make other pharmaceutical goods for the farming industry and is labeled hazardous by the EPA if spilled. I'm just looking for some direction on how it might need to be segregated and stored in regards to SQF Edition 8, if the program even allows it at all.