In its dry form, polyacrylamide is a white, granular substance that is stable and easy to handle. It is generally non-toxic when properly used, although the actual degree of toxicity can depend on the presence of residual acrylamide monomers. Therefore, it is crucial in its production and handling to adhere to safety guidelines to minimize any potential health risks.
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The process of developing an API typically involves several stages, including discovery, preclinical testing, and clinical trials. Once an API is developed and approved, it must be manufactured under stringent conditions in facilities that adhere to Good Manufacturing Practice (GMP) guidelines. Manufacturers must ensure that their APIs meet defined specifications for purity, potency, and consistency.