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Extractables are substances or compounds that can be extracted from a primary container, component material, delivery system or manufacturing surfaces when laboratory manipulation occurs (solvent or heat exposure), leading to contamination of pharmaceutical products. Extractables and leachables (E&L) testing is an Food and Drug Administration required step in filings of drug products or devices to determine what effect the packaging, delivery system, device materials or any other component that interacts with the drug or patient will have on it.